CARD9 mediates Dectin-1–induced ERK activation by linking Ras-GRF1 to H-Ras for antifungal

15 Pages·2014·2.48 MB·English

Article
CARD9 mediates Dectin-1–induced ERK
activation by linking Ras-GRF1 to H-Ras
for antifungal immunity
Xin-Ming Jia,1 Bing Tang,2 Le-Le Zhu,1 Yan-Hui Liu,1 Xue-Qiang Zhao,3
Sara Gorjestani,3 Yen-Michael S. Hsu,3 Long Yang,1 Jian-Hong Guan,1
Guo-Tong Xu,1 and Xin Lin3
1Research Center for Translational Medicine, Shanghai East Hospital, and Department of Immunology, Tongji University
School of Medicine, Shanghai 200120, China D
2Department of Burns, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China ow
n
3Department of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030 loa
d
e
d
ne from
i Dectin-1 functions as a pattern recognition receptor for sensing fungal infection. It has h
c ttp
di been well-established that Dectin-1 induces innate immune responses through caspase ://ru
e recruitment domain-containing protein 9 (CARD9)–mediated NF-B activation. In this pre
M study, we find that CARD9 is dispensable for NF-B activation induced by Dectin-1 ligands, ss.o
rg
l such as curdlan or Candida albicans yeast. In contrast, we find that CARD9 regulates H-Ras /jem
enta asicgtnivaal-tiroeng ublya tleindk pinrogt Reians -kGinRaFs1e t(oE RHK-)R aacst, iwvahtiicohn manedd ipatroesin Dfleacmtimn-a1to–riyn druescpeodn esxetsr wacheellnu lar /article-p
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m stimulated by their ligands. Mechanistically, Dectin-1 engagement initiates spleen tyrosine f/2
1
i kinase (Syk)–dependent Ras-GRF1 phosphorylation, and the phosphorylated Ras-GRF1 1/1
r 1
e recruits and activates H-Ras through forming a complex with CARD9, which leads to acti- /23
p 07
x vation of ERK downstream. Finally, we show that inhibiting ERK activation significantly accel- /12
1
E erates the death of C. albicans–infected mice, and this inhibitory effect is dependent on 1
5
of CARD9. Together, our studies reveal a molecular mechanism by which Dectin-1 induces 36/jem
H-Ras activation that leads to ERK activation for host innate immune responses against _
2
al fungal infection. 013
n 23
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ur 9.pd
Jo CXiOnR-MREinSPgO JNiaD: ENCE Ttehrne rimecmogunnieti osyns treemce upsteosr sg (ePrmRlRinse)- teon cseondseed v paarti-- PmRunRitsy tois ethlieciirt icnaflpaabmilmitya titoon a cantidva tien nmatuel tiimple- f by gu
he jOiaRx [email protected] ous pathogens including bacteria, viruses, and signaling cascades, leading to activation of var- est on
T Xin Lin: fungi, or endogenous danger signals, initiating ious transcription factors including NF-B 05
[email protected] intracellular signal cascades that result in the (Vallabhapurapu and Karin, 2009; Cargnello and Jan
u
a
Abbreviations used: Bcl10, activation of transcription factors, up-regulation Roux, 2011). ry 2
B cell leukemia-lymphoma 10; of defense-associated target genes, and release Dectin-1 is a Syk-coupled CLR and recog- 02
3
BMDC, BM-derived dendritic
of cytokines (Medzhitov, 2009). During fungal nizes -glucan carbohydrates on various fungi
cell; BMDM, BM-derived
macrophage; CARD9, caspase infection, the initial innate immune response including Candida albicans, Aspergillus fumigatus,
recruitment domain-containing is determined by the recognition of PAMPs and Pneumocystis carinii (Brown and Gordon, 2001;
protein 9; CLR, C-type lectin (pathogen-associated molecular patterns) by Steele et al., 2005; Saijo et al., 2007), whereas
receptor; CRD, extracellular
PRRs of innate immune cells (Romani, 2004). Dectin-2 and Dectin-3, two Syk-coupled
carbohydrate-binding domain;
ERK, extracellular signal- Several types of PRRs with signaling capacity CLRs, form heterodimeric PRR to recognize
regulated protein kinase; GDP, include TLRs, NLRs (nucleotide-oligomeriza- -mannans on the surface of C. albicans hyphae
guanosine diphosphate; GTPase,
tion domain-like receptors), RLRs (retinoic (Sato et al., 2006; Saijo et al., 2010; Zhu et al.,
guanosine triphosphatase;
ITAM, immunoreceptor tyro- acid-inducible gene I–like helicases), and the re- 2013). As the main nonopsonic receptor in-
sine-based activation motif; cently emerging family of spleen tyrosine kinase volved in fungal uptake (Heinsbroek et al., 2008),
Malt1, mucosa-associated lym-
(Syk)–coupled C-type lectin receptors (CLRs;
phoid tissue 1; PRR, pattern
recognition receptor; RLR, Kerrigan and Brown, 2011). The ability of these ©N o2n0c1o4m Jmiae recti aal–l. ShTahreis Aarlitkicel–eN ios dMisitrrriobru tSeidt eus nldiceer ntshee ftoerr mtsh eo ffi arsnt Astixtr ibmuotinotnh–s
retinoic acid-inducible gene I– after the publication date (see http://www.rupress.org/terms). After six months
like helicase; Syk, spleen X.-M. Jia, B. Tang, and L.-L. Zhu contributed equally to it is available under a Creative Commons License (Attribution–Noncommercial–
Share Alike 3.0 Unported license, as described at http://creativecommons.org/
tyrosine kinase. this paper. licenses/by-nc-sa/3.0/).
The Rockefeller University Press $30.00
J. Exp. Med. 2014 Vol. 211 No. 11 2307-2321 2307
www.jem.org/cgi/doi/10.1084/jem.20132349
Dectin-1 binds to -glucans from different fungal species previous study shows that stimulation of Dectin-1 with zymo-
(Brown and Gordon, 2001) and forms a phagocytic synapse san, curdlan, or HI C. albicans yeasts induces NF-B activation
complex on the cytoplasm membrane (Goodridge et al., 2011). through a CARD9-independent pathway in macrophages,
Dectin-1 collaborates with TLR2 (Ferwerda et al., 2008), whereas Dectin-2 stimulation by C. albicans hyphae triggers
SIGNR1 (Takahara et al., 2011), and galectin-3 (Esteban et al., NF-B activation through the CARD9-dependent pathway
2011) in recognizing -glucans on the surface of C. albicans (Bi et al., 2010). This study suggests that Dectin-1–induced sig-
yeast cells leading to induction of proinflammatory cytokines. naling may be more complicated than originally proposed
The caspase recruitment domain-containing protein 9 (Gross et al., 2006), and the molecular mechanism by which
(CARD9) is the critical adaptor protein that operates down- CARD9 is involved in Dectin-1 signaling pathway may need
stream of several immunoreceptor tyrosine-based activation to be further determined. Furthermore, a recent study also
motif (ITAM)–associated CLRs including Dectin-1, Dectin-2, shows that Dectin-1–induced signaling can module NF-B
and Mincle (Gross et al., 2006; Robinson et al., 2009; Bi through Raf-1–dependent phosphorylation and acetylation of
et al., 2010; Saijo et al., 2010; Schoenen et al., 2010). After re- p65 subunit of NF-B (Gringhuis et al., 2009), suggesting that
ceptor engagement and Syk kinase phosphorylation, CARD9 multiple signaling pathways may modulate Dectin-1–induced Do
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forms a complex with B cell leukemia-lymphoma 10 (Bcl10) NF-B activation. nlo
and mucosa-associated lymphoid tissue 1 (Malt1), which In this study, using Curdlan, a -glucan ligand and a mu- ade
d
transduces non–TLR signaling to the canonical NF-B path- tant C. albicans strain mnn5, which has the highly exposed sur- fro
m
way (Kingeter and Lin, 2012), leading to inducing the expres- face -glucans, we were able to examine the requirement of h
sion of proinflammatory cytokines, including TNF, IL-1, CARD9 for -glucan–induced signaling in innate immune cells ttp://ru
and IL-6. These proinflammatory cytokines control antifungal and found that although CARD9 is dispensable for Dectin-1– pre
immune responses (Netea et al., 1999; Vonk et al., 2006). More induced NF-B activation, it is required for Dectin-1–induced ss.o
importantly, the role of Dectin-1 and CARD9 in antifungal ERK activation by linking Ras-GRF1 to H-Ras. Together, rg/je
m
host defense has been confirmed by in vivo studies (Gross our studies reveal a molecular mechanism by which CARD9 /a
et al., 2006; Saijo et al., 2007; Taylor et al., 2007), together mediates Dectin-1-induced ERK activation for host anti- rticle
-p
with the discovery that host mutations in Dectin-1 or CARD9 fungal immune responses. df/2
1
lead to primary immunodeficiencies associated with fungal 1/1
1
infections (Ferwerda et al., 2009; Glocker et al., 2009). Thus, RESULTS /2
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CARD9 plays a central role in antifungal defense by receiving -glucans exposed on the surface of C. albicans yeast 7/1
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signals from Dectin-1 and Dectin-2 and stimulating proin- activate NF-B and ERK through Dectin-1 11
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flammatory responses. C. albicans is coated with mannoproteins that prevent -glucan 36
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However, most of the in vitro studies on Dectin-1 signal- moieties from being recognized by Dectin-1 on innate im- m
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ing have used -glucan–containing particles, such as zymosan mune cells (Gantner et al., 2005; Wheeler and Fink, 2006). To 01
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from Saccharomyces cerevisiae, curdlan from nonpathogenic study the effect of surface -glucans of live fungi on Dectin-1– 23
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bacteria, or heat-inactivated C. albicans yeasts as stimuli (Gross mediated innate immune responses, we generated a mutant .p
d
et al., 2006) because -glucans only become accessible at the strain of C. albicans, mnn5, in which the -1,2-mannosyltrans- f by g
site of budding scars in living C. albicans yeast cells (Gantner feranse gene MNN5 (Bai et al., 2006) was disrupted by homol- ue
et al., 2005). In addition, serum can induce a dimorphic tran- ogous recombination, thereby causing the increased exposure st o
n
0
sition of C. albicans from yeast to hyphae forms (Sevilla and of -glucans on the cell wall of C. albicans yeasts (Fig. 1 A). 5
Ja
Odds, 1986), which complicates the data interpretation of Consistently, the -glucan moiety on the surface of mnn5 yeast nu
a
in vitro studies of -glucan signaling through Dectin-1. Recent was more accessible to soluble GFP-tagged extracellular car- ry 2
0
studies showed that -glucans on the surface of C. albicans can bohydrate-binding domain (CRD) of Dectin-1 (sDectin-1CRD) 23
be unmasked by several experimental manipulations, such as than that on WT C. albicans yeast cells (Fig. 1 B).
heat-killing (Gantner et al., 2005), treatment with the anti- To further confirm that the exposed -glucan on the sur-
fungal drug caspofungin (Wheeler and Fink, 2006; Wheeler face of mnn5 yeast activates the signaling pathway through
et al., 2008), or deletion of certain Candida genes including Dectin-1, we stimulated BMDMs from WT (Clec7A+/+)
extracellular signal-regulated kinase gene CEK (Galán-Díez or Dectin-1–deficient (Clec7A/) mice with WT or mnn5
et al., 2010), the histidine kinase gene CHK1 (Klippel et al., yeast cells, and found that mnn5 yeasts induced more potent
2010), the predicted glucosyltransferase gene KRE5 (Wheeler NF-B DNA binding than WT yeast (Fig. 1 C), together with
and Fink, 2006), or the glycosidase gene PHR2 (Wheeler and more IB degradation (Fig. 1 D). Consistently, Dectin-1
Fink, 2006). Furthermore, unmasked -glucans of C. albicans deficiency impaired the NF-B activation (Fig. 1 C) and
can be specifically recognized by Dectin-1 and lead to more IB degradation (Fig. 1 D). Moreover, mnn5 yeasts triggered
potent activation of NF-B and extracellular signal-regulated stronger and sustained activation of ERK than WT yeast in
protein kinase (ERK) in human DCs (Wheeler and Fink, 2006; BMDMs (Fig. 1 D), but Dectin-1 deficiency significantly
Galán-Díez et al., 2010). impaired yeast-induced ERK activation in BMDMs (Fig. 1 D).
In contrast to the model that Dectin-1–induced NF-B In contrast, when these cells were stimulated with hyphal
is mediated through the CARD9-dependent pathway, our forms of C. albicans, NF-B activation (Fig. 1 E) and IB
2308 CARD9 regulates H-Ras activation. | Jia et al.
Article
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Figure 1. Surface -glucans on C. albicans yeasts activate NF-B and ERK through Dectin-1. (A and B) Surface -glucan accessibility on WT or
mnn5 yeast C. albicans strains, which were stained with anti–-1,3-glucan monoclonal antibodies (-glucan), followed by staining with FITC-labeled sec-
ondary antibodies (A) or soluble GFP-tagged Dectin-1 carbohydrate recognition domain (sDectin-1CRD; B). Bright field (BF), fluorescence (FL), and overlay
(right) are shown individually. Bars, 10 µm. (C and D) WT and Dectin-1 (Clec7A)–deficient BMDMs were stimulated with UV-inactivated WT yeasts or mnn5
yeasts (MOI = 5) for indicated times. Nuclear extracts were subjected to EMSA using 32P-labeled NF-B or Oct-1 probe (C). Cell lysates were subjected to
immunoblotting analysis using the indicated antibodies (D). (E and F) WT and Dectin-1 (Clec7A)–deficient BMDMs were stimulated with hyphae of WT
JEM Vol. 211, No. 11 2309
Figure 2. CARD9 engages the yeast-
induced ERK, but not NF-B activation.
(A and B) WT and CARD9-deficient BMDMs
(A) or BMDCs (B) were stimulated with UV-
inactivated WT or mnn5 strains of C. albicans
yeasts (MOI = 5) or hyphae (MOI = 1) for 1 h.
Nuclear extracts were prepared and subjected
to immunoblotting analysis using indicated
antibodies. (C and D) WT and CARD9-deficient
BMDMs (C) or BMDCs (D) were stimulated
with UV-inactivated WT or mnn5 mutant
strain of C. albicans yeast for the indicated
times. Cell lysates were prepared and sub-
jected to immunoblotting analysis using indi-
cated antibodies. (E) WT and CARD9-deficient
D
BMDMs were stimulated with UV-inactivated ow
n
mnn5 yeast cells (MOI = 5) for the indicated loa
d
times. Cell lysates were prepared and sub- ed
jected to immunoblotting analysis using fro
m
indicated antibodies. (F) WT and Bcl10- h
ttp
deficient BMDMs were stimulated with ://ru
UV-inactivated WT or mnn5 yeast cells pre
(MOI = 5) for the indicated times. Cell lysates ss.o
were prepared and subjected to immunoblot- rg
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ting analysis using indicated antibodies. Data m
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degradation and ERK activation (Fig. 1 F) were no different potent proinflammatory responses through Dectin-1, but not 21
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between WT and Dectin-1–deficient cells stimulated with Dectin-2, TLR2, or TLR4. 3
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WT or mnn5 mutant. These data indicate that mnn5 mutation /jem
_
does not increase the exposure of -glucan on the surface of CARD9 is required for the C. albicans yeast 20
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hyphae form of C. albicans; thereby Dectin-1 deficiency does stimulation-induced ERK but not NF-B activation 23
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not affect mnn5 hyphal form stimulation-induced signaling. Previous studies suggest that -glucans from C. albicans acti- 9.p
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We also found that blockade of Dectin-2 using its specific vate Dectin-1–mediated NF-B activation through a CARD9- f b
monoclonal antibodies (Zhu et al., 2013) in BMDMs had dependent pathway (Gross et al., 2006). To further investigate y gu
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almost no effect on NF-B activation induced by WT and mnn5 the role of CARD9 in Dectin-1–induced signaling pathways st o
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yeast stimulation (Fig. 1 G) and the production of proinflam- in response to fungal infection, BM-derived macrophages 05
matory cytokine TNF and IL-6 (Fig. 1 H). However, when (BMDMs) or BM-derived DCs (BMDCs) from WT (Card9+/+) Jan
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challenged with WT and mnn5 hyphae, blocking Dectin-2 or CARD9-deficient (Card9/) mice were stimulated with ary 2
completely inhibited NF-B activation (Fig. 1 G) and signifi- WT or mnn5 strain of C. albicans yeast. We found that CARD9 02
3
cantly reduced secretion of TNF and IL-6 (Fig. 1 H). Further- deficiency in BMDMs and BMDCs had no influences on the
more, deficiency of TRL2 or TLR4 had no influences on yeast stimulation-induced nuclear translocation of NF-B
WT and mnn5 yeast stimulation-induced activation of NF-B (p65 and p50 subunits; Fig. 2, A and B), as well as IB phos-
(Fig. 1 I) and ERK (Fig. 1, J and K). Together, these results in- phorylation and degradation (Fig. 2, C and D, top). In con-
dicate that the exposed -glucan on yeast surface can induce trast, when these cells were stimulated by C. albicans hyphae

yeasts or mnn5 (MOI = 1) for the indicated times. Nuclear extracts were subjected to EMSA using 32P-labeled NF-B or Oct-1 probe (E). Cell lysates were
subjected to immunoblotting analysis using the indicated antibodies (F). (G) WT BMDMs were stimulated with C. albicans WT or mnn5 yeast (MOI = 5) or
hyphae (MOI = 1) in the absence or presence of blocking antibodies against Dectin-2 (-Dectin-2, 20 µg/ml) for 60 min. Nuclear extracts were prepared
from these cells and subjected to immunoblotting analysis using indicated antibodies. (H) WT BMDMs were stimulated with the UV-inactivated yeast (MOI = 5) or
hyphae (MOI = 1) form of CAI4 or mnn5 mutant in the absence or presence of blocking antibodies against Dectin-2 (20 µg/ml) for 6 h. The amount of TNF
and IL-6 in the cultured media was determined using ELISA. **, P < 0.01; ***, P < 0.001. Data are means ± SD of triplicate wells and are representative of
three independent experiments. (I–K) WT, TLR2-, and TRL4-deficient BMDMs were stimulated with UV-inactivated WT (CAI4) or mnn5 strains of C. albicans
yeast cells (MOI = 5) for 1 h for preparing nuclear extracts (I) or for the indicated times for preparing cell lysates (J and K). Samples were subjected to im-
munoblotting analysis using indicated antibodies. Data shown are representative of three independent and reproducible experiments.
2310 CARD9 regulates H-Ras activation. | Jia et al.
Article
that activate Dectin-2 but not Dectin-1 signaling (Saijo et al., activated Dectin-1 or Dectin-2, respectively, leading to in-
2010), the nuclear translocation of NF-B subunits was de- duction of NF-B nuclear translocation and ERK phos-
fective in CARD9-deficient BMDMs (Fig. 2 A) and BMDCs phorylation (Fig. 3, A and B). Interestingly, we found that
(Fig. 2 B). Unlike the yeast stimulation-induced NF-B curdlan-induced ERK activation was defective in CARD9-
activation, we surprisingly found that C. albicans yeast stimula- deficient BMDMs and BMDCs (Fig. 3, C and D), whereas
tion-induced ERK phosphorylation was defective in CARD9- -mannan–induced ERK activation was intact (Fig. 3, C and D).
deficient BMDMs (Fig. 2 C, middle) and BMDCs (Fig. 2 D, Consistent with our previous findings (Bi et al., 2010),
middle), suggesting that CARD9 deficiency affects Dectin-1– curdlan-induced nuclear translocation of NF-B was intact
induced ERK activation. In addition, CARD9 deficiency had (Fig. 3, E and F). In contrast, -mannan–induced nuclear
no significant impact on Dectin-1–induced activation of p38 translocation of NF-B was defected in CARD9-deficient
and JNK MAP kinases (Fig. 2 E). Together, these results sug- cells (Fig. 3, E and F), which is consistent with our previous
gest that CARD9 may be dispensable for Dectin-1–induced studies that CARD9 is required for Dectin-2–induced NF-B
activation of NF-B, p38, and JNK, but it is required for Dectin-1– activation (Bi et al., 2010). Together, these results suggest that
induced ERK activation. CARD9 is required for Dectin-1–induced ERK activation but D
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Because CARD9 forms a complex with Bcl10 (Bertin is dispensable for NF-B activation. In contrast, CARD9 is n
lo
a
et al., 2000), we examined whether Bcl10 deficiency affected required for Dectin-2–induced NF-B activation. de
d
Dectin-1–induced ERK activation using BMDMs from WT fro
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or Bcl10-deficient (Bcl10/) mice, and found that Bcl10 CARD9 links Ras-GRF1 to H-Ras in response h
ttp
deficiency affected neither C. albicans yeast stimulation- to C. albicans yeast stimulation ://ru
induced IB phosphorylation and degradation nor ERK To determine the molecular mechanism by which CARD9 pre
activation (Fig. 2 F). This result suggests that although Dectin-1– is linked to the signaling pathway leading to activation of ss.o
rg
induced ERK activation is dependent on CARD9, it is in- ERK, we performed a Yeast Cyto-trap two-hybrid screen- /je
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dependent of the CARD9–Bcl10–Malt1 (CBM) complex ing. Multiple positive clones, which encode H-Ras (a member /a
(Kingeter and Lin, 2012). of Ras family of small guanosine triphosphatases [GTPases]) rticle
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and Ras-GRF1 (Ras-guanine-nucleotide-releasing factor 1), df/2
CARD9 is required for -glucan–induced ERK, were identified in this screening (unpublished data), suggest- 11
/1
but not NF-B, activation ing that CARD9 may associate with H-Ras and Ras-GRF1, 1/2
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It has been shown that Dectin-1 activates NF-B through which are upstream signaling components, leading to activation 07
/1
CARD9-dependent pathway (Gross et al., 2006), and curdlan, of ERK (Imamura et al., 2009; Wang et al., 2013). To examine 21
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a mixture of -glucan from nonpathogenic bacteria, is one of whether CARD9 is associated with H-Ras and Ras-GRF1, 36
/je
the ligands for Dectin-1 (Palma et al., 2006). To further deter- we immunoprecipitated CARD9 from RAW264.7 cells ex- m
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mine the role of CARD9 in Dectin-1 signaling, we used plate- pressing Flag-tagged CARD9 and found that immuno- 0
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bound curdlan or plate-bound -mannans, which potently precipitation of Flag-CARD9 effectively coprecipitated H-Ras 23
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Figure 3. CARD9 mediates Curdlan- n
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induced ERK activation but is not dispens- ry 2
able for NF-B. (A and B) RAW264.7 cells 02
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stably expressing human Dectin-1, Dectin-2,
or mock were stimulated with plate-coated
curdlan (50 µg/ml) or -mannans (40 µg/ml)
for 1 h for preparing nuclear extract (A) or
30 min for preparing cell lysate (B), and then
subjected to immunoblotting analysis using
the indicated antibodies. (C–F) WT and
CARD9-deficient BMDMs (C and E) or BMDCs
(D and F) were stimulated with plate-coated
curdlan (50 µg/ml) or -mannans (40 µg/ml)
for the indicated times for preparing cell
lysate (C and D) and 1 h for preparing nuclear
extract (E and F). The cell lysates or nuclear
extracts were subjected to immunoblotting
analysis using the indicated antibodies. Data
shown are representative of three indepen-
dent and reproducible experiments.
JEM Vol. 211, No. 11 2311
Figure 4. CARD9 links Ras-GRF1 to H-Ras in
response to C. albicans yeast stimulation.
(A) RAW264.7 cells stably expressing Flag-CARD9 were
stimulated with UV-inactivated WT or mnn5 yeast cells
for indicated times. Cell lysates (Ly) were immuno-
precipitated (IP) with anti-Flag antibody. (B) WT and
CARD9-deficient BMDMs were stimulated with UV-
inactivated mnn5 yeast cells for indicated times. Cell
lysates were immunoprecipitated with -CARD9 antibody.
The cell lysate or immunoprecipitates were subjected to
immunoblots using indicated antibodies. (C and D)
HEK293T cells were transfected with expression vectors
encoding Ras-GRF1, Myc-H-Ras, and Flag-CARD9 at
different combinations. Cell lysates were subjected to
immunoprecipitation with anti-Flag (C) or anti-Ras-
D
GRF1 antibody (D). (E) WT and CARD9-deficient BMDMs ow
n
were stimulated with UV-inactivated mnn5 yeast cells loa
d
for indicated times. Cell lysates were immunoprecipi- ed
tated with anti–H-ras antibody. Immunoprecipitated (IP) fro
m
and lysate (Ly) fractions were analyzed by immunoblot- h
ttp
ting using the indicated antibodies. (F) WT and CARD9- ://ru
deficient BMDMs were stimulated with UV-inactivated p
re
mnn5 yeast cells or EGF (as a control) for indicated ss.o
times. Ras activation was determined by pull-down assay rg
/je
using a Ras activation assay Biochem kit according to m
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tthotea ml aanndu faaccttivuarteerd’s Rinasst rwuacsti opnersf. oImrmmeudn fooar sdseatye ormf tinhien g rticle-p
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the Ras activation. Data shown are representative of f/2
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three independent and reproducible experiments. 1/1
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and Ras-GRF1 after the stimulation by WT C. albicans yeast with H-Ras (Fig. 4 E). These results suggest that CARD9 20
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(Fig. 4 A). Consistently, mnn5 yeast stimulation induced a bridges the interaction between Ras-GRF1 and H-Ras, which 23
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stronger association of CARD9 with both H-Ras and Ras- leads to activation of downstream signaling. Because Ras- 9.p
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GRF1 (Fig. 4 A), suggesting that CARD9 inducibly forms a GRF1 activates H-Ras (Zhu et al., 2007), we examined H-Ras f b
complex with H-Ras and Ras-GRF1 in Dectin-1–induced activation and found that H-Ras could be effectively acti- y gu
e
signaling cascade. vated by C. albicans stimulation, whereas CARD9 deficiency st o
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To further confirm the inducible association of CARD9 impaired this activation (Fig. 4 F). Together, these results indi- 05
with H-Ras and Ras-GRF1, endogenous CARD9 was cate that CARD9 mediates H-Ras activation through bridg- Jan
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immunoprecipitated from BMDMs after stimulation by ing Ras-GRF1 to H-Ras. ry 2
C. albicans yeasts. We found that CARD9 inducibly coimmuno- 02
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precipitated with both H-Ras and Ras-GRF1 after stimu- Stimulation of Dectin-1 by C. albicans yeast induces ERK
lation (Fig. 4 B), and this association was specific because activation though CARD9-bridged Ras-GRF1–H-Ras complex
CARD9 deficiency abolished this association (Fig. 4 B). To determine whether the formation of CARD9-bridged
Together, these results suggest that CARD9 associates with Ras-GRF1 and H-Ras complex is dependent on Dectin-1-
H-Ras and Ras-GRF1 in response to the stimulation of C. induced signaling, we examined this complex formation after
albicans yeasts. C. albicans yeast stimulation in WT (Clec7A+/+) and Dectin-1–
Interestingly, CARD9 constitutively associated with deficient (Clec7A/) BMDMs, and found that this com-
H-Ras or Ras-GRF1 when they were coexpressed in plex was completely defective in Dectin-1–deficient cells
HEK293T cells (Fig. 4 C). However, the association of (Fig. 5 A). Consistently, C. albicans yeast stimulation-induced
CARD9 with H-Ras was significantly enhanced when three H-Ras activation was completely defective in Dectin-1–
of them were coexpressed in 293T cells (Fig. 4 C). Similarly, deficient BMDMs (Fig. 5 B). In addition, treatment of
although Ras-GRF1 weakly associated with H-Ras, this as- BMDMs with Syk inhibitor Piceatannol also blocked this com-
sociation was significantly enhanced upon coexpression of plex formation (Fig. 5 C), and the yeast-induced phosphory-
them with CARD9 (Fig. 4 D). Consistently, CARD9 defi- lation of Ras-GRF1 as well as ERK activation (Fig. 5 D).
ciency impaired the yeast-induced association of Ras-GRF1 In contrast, CARD9 deficiency did not significantly impair
2312 CARD9 regulates H-Ras activation. | Jia et al.
Article
Figure 5. Dectin-1/Syk stimulation by
C. albicans yeast induces the formation of a
Ras-GRF1–CARD9–H-Ras complex. (A) WT
and Dectin-1–deficient BMDMs were stimu-
lated with UV-inactivated mnn5 yeast cells
(MOI = 5) for the indicated times. Cell lysates
were immunoprecipitated with anti-CARD9
antibody and immunoprecipitated (IP) and
lysate (Ly) fractions were analyzed by immuno-
blotting using indicated antibodies. (B) WT
and Dectin-1–deficient BMDMs were stimu-
lated with UV-inactivated mnn5 yeast cells
(MOI = 5) or EGF for indicated times. Ras
activation was determined by pull-down assay
using a Ras activation assay Biochem kit.
D
Immunoassay of the total and activated Ras ow
n
was performed for determining the Ras acti- lo
a
d
vation. (C) RAW264.7 cells stably expressing ed
Flag-Card9 were pretreated with or without fro
m
Syk inhibitor (piceatannol) for 30 min before h
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stimulation with UV-inactivated mnn5 yeast ://ru
cells (MOI = 5) for indicated times. Cell lysates p
re
were immunoprecipitated with anti-Flag anti- ss.o
body and analyzed by immunoblotting using rg
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indicated antibodies. (D) WT BMDMs were m
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p30re mtreina tbeedf owreit hst iomr uwlaitthioonu tw pitihce UaVta-ninnaoclt ifvoart ed rticle-p
d
mnn5 yeast cells (MOI = 5) for the indicated f/2
1
times. (E) WT and CARD9-deficient BMDMs 1/1
1
were stimulated with UV-inactivated mnn5 /2
3
yeast cells (MOI = 5) for the indicated times. 07
/1
(F) WT and CARD9-deficient BMDMs were 21
1
stimulated with UV-inactivated mnn5 yeast 53
6
cells for indicated times. Cell lysates were /je
m
immunoprecipitated with anti-Ras-GRF1 _2
0
antibody and immunoprecipitated (IP) and 13
2
lysate (Ly) fractions were analyzed by immuno- 34
9
blotting using indicated antibodies. (G) WT .pd
and CARD9-deficient BMDMs were stimulated f by g
with plate-coated curdlan (50 µg/ml) for the ue
indicated times. (H and I) Knockdown of st o
n
endogenous H-Ras by RNA interference in 0
5
BMDMs, which were transfected with siRNA Ja
n
u
against murine H-Ras and nontargeting con- a
trol siRNA using Trans IT-TKO transfection reagent (Mirus). Cells were cultured for 48 h after transfection and then stimulated with plate-coated curdlan ry 20
2
(50 µg/ml), UV-inactivated mnn5 yeast cells (MOI = 5), plate-coated -mannans (50 µg/ml), or LPS (100ng/ml) for the indicated times. Cell lysates were 3
subjected to immunoblotting analysis using indicated antibodies. Data shown are representative of three independent and reproducible experiments.
the yeast-induced Ras-GRF1 phosphorylation (Fig. 5, E and F), through scaffold protein CARD9, leading to the activation of
indicating that CARD9 functions downstream of Ras-GRF1. ERK pathway.
Similarly, CARD9 deficiency significantly impaired curdlan-
induced phosphorylation of ERK, but not Ras-GRF1 (Fig. 5 G), The CARD9/H-Ras/ERK signaling cascade is critical
indicating that CARD9 functions downstream of Ras-GRF1. for immune responses triggered by C. albicans yeast
Consistently, knockdown of endogenous H-Ras in BMDMs To determine the functional effect of CARD9 on Dectin-1–
specifically inhibited curdlan- or yeast-induced phosphory- induced cytokine production, we first treated C. albicans yeasts
lation of ERK (Fig. 5 H) but had no effect on -mannans– with UV light that fixes C. albicans at the yeast stage and pre-
or LPS-induced ERK activation (Fig. 5 I). Together, these vents them from transforming into hyphae, and then stimu-
results demonstrate that Dectin-1 signaling activated by lated WT or CARD9-deficient BMDMs with UV-inactivated
-glucans induces Syk-dependent phosphorylation of Ras- C. albicans yeast cells. We found that secretion of cytokines
GRF1, and then the phosphorylated Ras-GRF1 activates H-Ras including TNF, IL-6, and IL-1 had a significant reduction,
JEM Vol. 211, No. 11 2313
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Figure 6. CARD9-mediated H-Ras activation is critical for immune responses triggered by C. albicans yeast and curdlan. (A and B) ELISA results
for cytokines TNF, IL-1, IL-6, and IL-12p40 in supernatants of WT and CARD9-deficient BMDMs, which were stimulated for 6 h with UV-inactivated WT
or mnn5 yeast (MOI = 5; A) or hyphae (MOI = 0.1; B). (C and D) ELISA results for cytokines TNF, IL-1, IL-6, and IL-12p40 in supernatants of WT and
CARD9-deficient BMDMs, which were pretreated with or without 5 µM U0126 for 30 min and then stimulated with UV-inactivated mnn5 yeast cells
(MOI = 5; C) or plate-coated curdlan (50 µg/ml; D) for 6 h. (E and F) ELISA results for cytokines TNF, IL-1, IL-6, and IL-12p40 in supernatants of WT BMDMs,
which were transfected with siRNA against murine H-Ras and nontargeting control siRNA using Trans IT-TKO transfection reagent (Mirus). Cells were
cultured for 48 h after transfection and then stimulated with plate-coated curdlan (50 µg/ml), UV-inactivated mnn5 yeast cells (MOI = 5), plate-coated
2314 CARD9 regulates H-Ras activation. | Jia et al.
Article
whereas IL-12 production was only slightly affected in To further confirm the effect of CARD9-mediated im-
CARD9-deficient BMDMs (Fig. 6 A). In contrast, when mune responses on the clearance ability to systemic C. albicans
BMDMs were stimulated with C. albicans hyphae, which in- infections, we challenged WT or CARD9-deficient mice with
duces proinflammatory signaling through the Dectin-2– and UV-inactivated WT (CAF2-1) or mnn5 mutant C. albicans.
Dectin-3–dependent pathways (Saijo et al., 2010; Zhu et al., Similar to the in vitro challenging of macrophages by UV-
2013), CARD9 deficiency was significantly impaired in the inactivated C. albicans (Fig. 6 A), CARD9-deficient mice had
expression of these cytokines (Fig. 6 B). Furthermore, we ex- significantly lower levels of TNF, IL-6, and IL-1 production
amined the effect of inhibiting ERK signaling on cytokine in their serum at day 2 after infected with mnn5 mutant,
production by WT or CARD9-deficient BMDMs, which but only TNF production had a significant reduction when
were treated with or without U0126, an inhibitor for ERK infecting CARD9-deficient mice with CAF2-1 strain (Fig. 7 E).
activation. We found that U0126 significantly suppressed TNF, To determine the role of Dectin-2–mediated host defense
IL-6, and IL-1 production by WT BMDMs in response against systemic infections with mnn5 mutant, mice receiving
to Dectin-1 agonists C. albicans yeast (Fig. 6 C) and curdlan anti–Dectin-2 or nonspecific control IgG were intravenously
(Fig. 6 D). However, U0126 treatment did not significantly injected with a sublethal dose (6 × 104) of WT (CAF2-1) or D
o
w
affect the expression of these cytokines in CARD9-deficient mnn5 mutant strains. Blocking Dectin-2 significantly de- n
lo
a
BMDMs after the stimulation by C. albicans yeast (Fig. 6 C) or creased the survival rate of CAF2-1–infected mice (P < 0.01; de
d
curdlan (Fig. 6 D), suggesting that the inhibited signaling by Fig. 7 F) but had very little impact on mnn5 mutant-infected fro
m
U0126 may be largely overlapped with CARD9-induced sig- mice (Fig. 7 F). The fungal burden in kidney of these mice h
ttp
naling. Consistent with the effect on CARD9-deficient consistently showed similar phenotypes (Fig. 7 G). Together, ://ru
on TNF and IL-6 production, knockdown of endogenous these data suggest that mnn5 mutant C. albicans is virulent to pre
H-Ras in BMDMs also significantly reduced curdlan- or CARD9-deficient mice, and that the faster clearance of mnn5 ss.o
rg
yeast-induced production of TNF and IL-6 (Fig. 6 E). As mutant of C. albicans by WT mice may be due to a stronger /je
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controls, U0126 treatment and knockdown of endogenous activation of -glucan–induced Dectin-1–, but not Dectin-2–, /a
H-Ras in BMDMs had no effect on -mannans– or LPS- and CARD9-dependent inflammatory responses. rticle
-p
induced secretions of TNF, IL-6, IL-1, and IL-12 (Fig. 6, To determine the contribution of CARD9-mediated df/2
F and G). Together, these results suggest that the activation ERK activation on antifungal immunity in vivo, we pretreated 11
/1
of CARD9-mediated H-Ras/ERK cascade induced by WT or CARD9-deficient mice with or without U0126, and 1/2
3
Dectin-1 agonist is critical for the production of proinflam- then intravenously infected these mice with a low dose (5 × 07
/1
matory cytokines. 104) of mnn5 mutant. We found that administration of U0126 21
1
5
reduced the survival rate of WT mice (P < 0.05; Fig. 8 A). 36
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However, administration of U0126 did not have a significant m
_
2
ERK activation is critical for CARD9-mediated effect on the survival of CARD9-defecient mice (P > 0.05; 0
1
3
innate immunity against C. albicans Fig. 8 A). Consistently, U0126 treatment only significantly 23
4
To examine the effect of -glucan exposed on the surface affected the fungal load (P < 0.01; Fig. 8 B) and cytokine 9.p
d
of C. albicans yeast on host immune responses, we compared production (Fig. 8 C) in the kidney of WT but not CARD9- f b
y g
the pathogenicity of WT, mnn5 mutant, and MNN5-reconsti- defecient mice after mnn5 infection, suggesting that the con- u
e
tuted mnn5 strains (mnn5/MNN5) of C. albicans in a murine tribution of ERK activation on antifungal immunity is largely st o
n
model of systemic candidiasis. Consistent with a previous dependent on CARD9-mediated signaling. 05
report (Bai et al., 2006), mnn5 mutant-infected mice sur- Jan
u
a
vived significantly longer than CAF2-1 (the parental strain of ry 2
C. albicans)– or mnn5/MNN5-infected mice with a lethal dose DISCUSSION 02
3
(1 × 106) of C. albicans (Fig. 7 A). The fungal burdens of kid- During C. albicans infection, both yeast and hyphae forms
neys in mice infected with mnn5 mutant were significantly can be found in infected tissues, and innate immune cells
lower than those infected with either CAF2-1 or mnn5/ discriminate them through different PRRs, especially CLRs,
MNN5 strains (P < 0.01, Fig. 7 B). However, we found that which elicit protective immune responses against this infec-
all CARD9-deficient mice died within 5 d after infection tion. Previous studies have shown that CARD9, a scaffold
with a sublethal dose (3 × 105) of WT (CAF2-1) or mnn5 protein, is required to mediate different CLR-induced NF-B
mutant strains of C. albicans (P > 0.05, Fig. 7 C) and, consis- activation after fungal infection. In this study, we found that
tently, fungal burden in the kidney of CARD9-deficient mice CARD9 is dispensable for Dectin-1–induced NF-B activation
had no significant difference when challenging with CAF2-1 but it is required for Dectin-1–induced ERK activation with
or mnn5 strains (P > 0.05, Fig. 7 D). stimulation of C. albicans yeasts, whereas Dectin-2–induced

-mannans (50 µg/ml), or LPS (100 ng/ml) for 6 h. (G) ELISA results for cytokines TNF, IL-1, IL-6, and IL-12p40 in supernatants of WT and CARD9-deficient
BMDMs, which were pretreated with or without 5 µM U0126 for 30 min and then stimulated with plate-coated -mannans (50 µg/ml) or LPS (100 ng/ml)
for 6 h. *, P < 0.05; **, P < 0.01; ***, P < 0.001. Data are means ± SD of triplicate samples and are representative of three independent experiments.
JEM Vol. 211, No. 11 2315
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Fdiigduiarsei s7. .( A aSnudr fBa)c Ien fe-ctgeldu cmaincse esxuprvoisveadl aonnd Ck.id anlebyic CaFnUs asisgsanyifi. Gcaronutplys eonf hCa5n7cBe/ LC6A feRmD9al-em meidceia wteedr ep irnojiencflteadm vmiaa ltaitoenra rl etsapilo vnesines w aigtha i1n s×t 1s0y6s tCeFmUi co fc an- est on
0
C. albicans WT (CAF2-1), mnn5 mutant, and its restored strain (mnn5/MNN5) in 200 µl sterile saline. Survival of these mice (n = 10 per group) was monitored 5 Ja
and plotted (A). Kidney CFU assay (n = 5 per group) was performed at day 2 after infection (B). Shown are means and SD for n = 3. (C and D) WT (Card9+/+; nu
a
squares) and CARD9-deficient mice (Card9/; triangles) were infected intravenously with 3 × 105 CFU of C. albicans WT (CAF2-1) and mnn5 mutant strains ry 2
in 200 µl sterile saline. Survival of these mice (n = 10 per group) was monitored and plotted (C). Kidney CFU assay (n = 5 per group) was performed at 02
3
day 2 after infection (D). Shown are means and SD for n = 3. (E) ELISA results for TNF, IL-6, IL-1, and IL-12p40 in mouse sera at day 2 after infection.
WT (Card9+/+) and CARD9-deficient (Card9/) mice (n = 5 per group) were challenged with UV-inactivated C. albicans WT (CAF2-1) and mnn5 mutant yeast
cells (1 × 106) in 200 µl sterile saline. Data shown are representative of three independent experiments. SDs are indicated. (F and G) Infected mice survival
and kidney CFU assay. Groups of C57B/L6 female mice infected with 6 × 104 CFU of C. albicans WT (CAF2-1) and mnn5 mutant strains, which were treated
with 200 µg anti–Dectin-2 monoclonal antibodies (-D2) or nonspecific control IgG per mouse for four times at 6 h before or 2, 4, or 6 d after injection of
C. albicans. Survival of these mice (n = 10 per group) was monitored and plotted (F). Kidney CFU assay (n = 5 per group) was performed at day 2 after infec-
tion (G). Shown are means and SD for n = 5. Two independent experiments were conducted (n = 10 in each group). *, P < 0.05; **, P < 0.01; ***, P < 0.001.
NF-B activation is completely dependent on CARD9 with In this study, we have also found that CARD9-mediated
stimulation of C. albicans hyphae. Mechanistically, we found signaling had more significant contributions to Dectin-2–
that CARD9 links Ras-GRF1 to H-Ras and regulates the mediated proinflammatory responses than those mediated
activation of H-Ras, leading to activation of downstream by Dectin-1, including induction of IL-1 and IL-6, two
ERK activation. Together, we have revealed a previously un- pivotal cytokines for priming downstream Th17 differentia-
known mechanism by which Dectin-1 induces H-Ras acti- tion. Consistent with our observations, CARD9 has been
vation that, in turn, induces downstream ERK activation. shown to be indispensable for development of Th17 responses
2316 CARD9 regulates H-Ras activation. | Jia et al.