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Stem Cells in Endocrinology PDF

277 Pages·2005·4.862 MB·English
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CONTEMPORARY ENDOCRINOLOGY™ SStteemm CCeellllss iinn EEnnddooccrriinnoollooggyy EEddiitteedd bbyy LLiinnddaa BB.. LLeesstteerr,, MMDD S C E TEM ELLS IN NDOCRINOLOGY C E ONTEMPORARY NDOCRINOLOGY P. Michael Conn, S E ERIES DITOR Stem Cells in Endocrinology, edited by Assisted Fertilization and Nuclear Transfer LINDA B. LESTER, 2005 in Mammals, edited by DON P. WOLF Office Andrology, edited by PHILLIP E. AND MARY ZELINSKI-WOOTEN, 2001 PATTON AND DAVID E. BATTAGLIA, 2005 Adrenal Disorders, edited by ANDREW N. Male Hypogonadism: Basic, Clinical, and MARGIORIS AND GEORGE P. CHROUSOS, Therapeutic Principles, edited by 2001 STEPHEN J. WINTERS, 2004 Endocrine Oncology, edited by STEPHEN P. Androgens in Health and Disease, edited ETHIER, 2000 by CARRIE J. BAGATELL AND WILLIAM J. Endocrinology of the Lung: Development BREMNER, 2003 and Surfactant Synthesis, edited by Endocrine Replacement Therapy in Clinical CAROLE R. MENDELSON, 2000 Practice, edited by A. WAYNE MEIKLE, Sports Endocrinology, edited by MICHELLE P. 2003 WARREN AND NAAMA W. CONSTANTINI, 2000 Early Diagnosis of Endocrine Diseases, Gene Engineering in Endocrinology, edited edited by ROBERT S. BAR, 2003 by MARGARET A. SHUPNIK, 2000 Type I Diabetes: Etiology and Treatment, Endocrinology of Aging, edited by JOHN E. edited by MARK A. SPERLING, 2003 MORLEY AND LUCRETIA VAN DEN BERG, 2000 Handbook of Diagnostic Endocrinology, Human Growth Hormone: Research and edited by JANET E. HALL AND LYNNETTE Clinical Practice, edited by ROY G. K. NIEMAN, 2003 SMITH AND MICHAEL O. THORNER, 2000 Pediatric Endocrinology: A Practical Hormones and the Heart in Health and Clinical Guide, edited by SALLY Disease, edited by LEONARD SHARE, 1999 RADOVICK AND MARGARET H. Menopause: Endocrinology and Management, MACGILLIVRAY, 2003 edited by DAVID B. SEIFER AND Diseases of the Thyroid, 2nd ed., edited by ELIZABETH A. KENNARD, 1999 LEWIS E. BRAVERMAN, 2003 The IGF System: Molecular Biology, Developmental Endocrinology: From Physiology, and Clinical Applications, Research to Clinical Practice, edited edited by RON G. ROSENFELD AND by ERICA A. EUGSTER AND ORA HIRSCH CHARLES T. ROBERTS, JR., 1999 PESCOVITZ, 2002 Neurosteroids: A New Regulatory Function Osteoporosis: Pathophysiology and Clinical in the Nervous System, edited by Management, edited by ERIC S. ETIENNE-EMILE BAULIEU, MICHAEL ORWOLL AND MICHAEL BLIZIOTES, 2002 SCHUMACHER, AND PAUL ROBEL, 1999 Challenging Cases in Endocrinology, Autoimmune Endocrinopathies, edited by edited by MARK E. MOLITCH, 2002 ROBERT VOLPÉ, 1999 Selective Estrogen Receptor Modulators: Hormone Resistance Syndromes, edited by Research and Clinical Applications, J. LARRY JAMESON, 1999 edited by ANDREA MANNI AND MICHAEL Hormone Replacement Therapy, edited by F. VERDERAME, 2002 A. WAYNE MEIKLE, 1999 Transgenics in Endocrinology, edited by Insulin Resistance: The Metabolic Syndrome X, MARTIN MATZUK, CHESTER W. BROWN, edited by GERALD M. REAVEN AND AMI LAWS, AND T. RAJENDRA KUMAR, 2001 1999 S C TEM ELLS E IN NDOCRINOLOGY Edited by L B. L , , INDA ESTER MS MD Division of Endocrinology, Diabetes and Clinical Nutrition Department of Medicine, Oregon Health and Sciences University Portland, Oregon © 2005 Humana Press Inc. 999 Riverview Drive, Suite 208 Totowa, New Jersey 07512 humanapress.com For additional copies, pricing for bulk purchases, and/or information about other Humana titles,contact Humana at the above address or at any of the following numbers: Tel: 973-256-1699;Fax: 973-256-8341; E-mail: humana@ humanapr.com.com or visit our website at humanapress.com All rights reserved. No part of this book may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, microfilming, recording, or otherwise without written permission from the Publisher. All articles, comments, opinions, conclusions, or recommendations are those of the author(s), and do not necessarily reflect the views of the publisher. Due diligence has been taken by the publishers, editors, and authors of this book to assure the accuracy of the information published and to describe generally accepted practices. The contributors herein have carefully checked to ensure that the drug selections and dosages set forth in this text are accurate and in accord with the standards accepted at the time of publication. Notwithstanding, as new research, changes in government regulations, and knowledge from clinical experience relating to drug therapy and drug reactions constantly occurs, the reader is advised to check the product information provided by the manufacturer of each drug for any change in dosages or for additional warnings and contraindications. This is of utmost importance when the recommended drug herein is a new or infrequently used drug. It is the responsibility of the treating physician to determine dosages and treatment strategies for individual patients. Further it is the responsibility of the health care provider to ascertain the Food and Drug Administration status of each drug or device used in their clinical practice. The publisher, editors, and authors are not responsible for errors or omissions or for any consequences from the application of the information presented in this book and make no warranty, express or implied, with respect to the contents in this publication. This publication is printed on acid-free paper. (cid:39) ANSI Z39.48-1984 (American National Standards Institute) Permanence of Paper for Printed Library Materials. Production Editor: Anne Peters Cover Design: Patricia Cleary Cover illustration from Fig. 5, Chapter 5, “Growth Conditions for Primate vs Murine Embryonic Stem Cells,” by Gillian M. Beattie, Nathan Bucay, Rohan Humphrey, Ana D. Lopez, and Alberto Hayek Photocopy Authorization Policy: Authorization to photocopy items for internal or personal use, or the internal or personal use of specific clients, is granted by Humana Press Inc., provided that the base fee of US $30.00 per copy is paid directly to the Copyright Clearance Center at 222 Rosewood Drive, Danvers, MA 01923. For those organizations that have been granted a photocopy license from the CCC, a separate system of payment has been arranged and is acceptable to Humana Press Inc. The fee code for users of the Transactional Reporting Service is: [1-58829-407-2/05 $30.00]. Printed in the United States of America. 10 9 8 7 6 5 4 3 2 1 e-ISBN:1-59259-900-1 Library of Congress Cataloging-in-Publication Data Stem cells in endocrinology / edited by Linda B. Lester. p. cm. -- (Contemporary endocrinology) Includes bibliographical references and index. ISBN 1-58829-407-2 (alk. paper) 1. Stem cells. 2. Endocrinology, Experimental. I. Lester, Linda B. II. Series: Contemporary endocrinology (Totowa, N.J.) QH588.S83S747 2005 616'.02774--dc22 2004017508 Dedication The lights of stars that were extinguished ages ago still reach us. So it is with great men who died centuries ago, but still reach us with the radiations of their personalities. — KHALIL GIBRAN The recent death of James R. Hansen, MD (August 24, 1951 to May 27, 2003) cut short a life dedicated to family, patients, and a cure for type 1 diabetes. After medical school at Oregon Health Sciences University, Jim completed a pediatric residency and pediatric endocrine fellowship at the University of Iowa. Upon returning to Portland, Oregon, Jim became medical director of the Emanuel Children’s Diabetes and Endocrine Center. There he worked passionately to care for his patients with type 1 diabetes and continued to pursue novel diabetes thera- pies through ongoing clinical research. Jim was actively involved with the Juvenile Diabetes Research Foundation (JDRF) at both the local and interna- tional levels. He was very enthusiastic about the use of stem cells for endocrine therapies, particularly for treating patients with type 1 diabetes. Jim served as the committee chair for the JDRF’s Human Stem Cell Research Committee up until a few weeks before his death. This book is dedicated to Dr. James Hansen, in memory of his life, vision, and inspiration. He continues to shine for those of us he touched. v Preface As the world population ages, health care costs are expected to escalate as a result of the increase in age-related, degenerative diseases. Regenerating the failing cells and organs associated with these diseases would preserve quality of life and help curtail the increase in health care costs. Medical scientists today are faced with the challenge of developing new and innovative regenerative thera- pies to meet this need. A major focus of this research is to identify sources of cells and tissues that can be used in regenerative therapies. Stem cells, by definition, can self-replicate and, under the right conditions, differentiate into mature cell phenotypes. Stem cells are a potential source of cells for regenerative medical therapies, and research on defined stem cell populations will facilitate the study of organ development ex vivo. Understanding stem cell growth and development will shed light on the biological process of tissue/organ development and likely lead to novel regenerative therapies. Although all stem cells have a limited capacity for self-replication and differ- entiation, some stem cells are capable of differentiating into multiple cell types, a property known as plasticity. Embryonic stem (ES) cells are derived from the early blastocyst and contain stem cells capable of generating all adult tissues. This makes ES cells the most pluripotent, or plastic, of the available stem cells. Recently, ES cell lines were derived from animal and human blastocysts. These cell lines are capable of self-replication and can be expanded in culture to provide a renewable source of cells. Human ES cell lines are an invaluable research tool for the study of human development in vitro. In addition, human ES cells have the potential for direct use in therapies; thus, these cell lines represent a major advance in cell biology that will have a broad impact on subsequent medical research. The study of stem cell biology is likely to have profound effects for the near future, affecting the current equilibrium in medical research. The evolution of science and medicine is punctuated by events that are clearly so significant that they alter the future course of scientific and medical discovery. The derivation of human ES cell lines, in my mind, is clearly such an event. Human ES cell lines, along with other stem cell lines, will have broad and long-lasting effects on developmental biology and translational research. However, the fundamental importance of ES cell lines does not necessarily imply that ES cells will become vii viii Preface the cell source for regenerative medicine. The appropriate stem cells will need to be evaluated for each disease system that may benefit from regenerative therapy. Many disease processes stand to benefit from regenerative medical therapies, including disorders of the central nervous system, cardiovascular, gastrointestinal, and hematologic systems. Currently, some of these disorders can be treated using whole organ transplantation. However, whole organ transplantation is limited to a small percent of patients because of the scarcity of organs for donation and the need for broad spectrum immunosuppressive therapies. As opposed to other systems, degenerative disorders of the endocrine system can currently be treated using exogenous hormonal therapies. These therapies, however, are frequently inadequate, resulting in significant morbidity and mortality to patients. The difficulty in treating endocrine disorders is developing a therapy that mimics the natural feedback mechanisms inherent to functional endocrine organs. Most current exogenous endocrine therapies fail to mimic the precise metabolic control of endog- enous hormone release, resulting in under- or overtreatment and thereby leading to complications. This is clearly illustrated by the persistent complications of diabetes in patients on exogenous insulin therapy. Replacing endocrine organ function with functionally responsive cells will allow for the precise regulation of hormone release through natural feedback and should dramatically improve medical care. The recent success of islet transplantation indicates the potential for cell therapies to improve medical care for patients with diabetes. Again, the major drawback is the lack of tissue available for these procedures. The shortage of islets and other endocrine tissues could be overcome by developing alternative tissue sources such as the use of stem cells. Endocrine diseases, in particular diabetes, are therefore prime targets for stem cell therapeutics. The objective of this text is to provide a primary source of information on basic stem cell biology and the application of stem cell research to endocrine diseases. As such, this book should be useful for both clinical endocrinologists and endo- crine researchers alike. The information in this book is divided into two main sections: first, a basic stem cell biology section and second, translational stem cell research with endocrine applications. In the basic science section, each of the major sources of stem cells are discussed, including embryonic, cord blood, germ line, and adult stem cells tissues. Because it is not clear which stem cell types will eventually be used for endocrine therapies discussing all stem cells allows a side-by-side comparison of the different stem cell types and a full understanding of the pros and cons of each. The second section explores how stem cells may be employed to develop endocrine-related cells or tissues. This includes discus- sions on directed differentiation using transgenes and development of endocrine- specific phenotypes including (cid:96)-cells, hepatocytes, bone, and sperm. Because Preface ix many endocrine disorders are autoimmune mediated, we also include a discus- sion of stem cell therapy for the treatment of autoimmune disorders. In the future, stem cell therapies for thyroid and other endocrine disorders may be available, but these areas are not discussed given the limited amount of research currently available. In closing, I would like to thank all the contributing authors for taking time from their research efforts to share their thoughts and ideas in this book. Their collective expertise provides an excellent starting point for the endocrine researcher, illuminating the complexity and potential of stem cell research in endocrinology. I also want to thank Drs. Laura Andrews and Brian Nauert for their thoughts, editorial comments, and efforts in my research lab while I was working on this project. Finally, I would like to thank Dr. Lynn Loriaux for his ongoing support of stem cell research at Oregon Health and Sciences University and my family, for enduring cold dinners and late nights with few complaints. I could not flourish without their support and encouragement. My accomplish- ments are clearly a reflection of all those around me. Linda B. Lester, MS, MD Contents Dedication.....................................................................................v Preface ....................................................................................... vii Contributors.............................................................................. xiii P I: B S C B ART ASIC TEM ELL IOLOGY 1 Embryonic Stem Cells: Derivation, Properties, and Therapeutic Implications ...........................................3 Victoria L. Browning and Jon S. Odorico 2 Germ Line Stem Cells ..........................................................23 Makoto C. Nagano 3 Umbilical Cord Stem Cells...................................................49 Kathy E. Mitchell 4 Differentiation Potential of Adult Stem Cells......................67 Henry E. Young and Asa C. Black, Jr. 5 Growth Conditions for Primate vs Murine Embryonic Stem Cells........................................................................93 Gillian M. Beattie, Nathan Bucay, Rohan Humphrey, Ana D. Lopez, and Alberto Hayek P II: T R ART RANSLATIONAL ESEARCH 6 Islet Precursor Cells in Adult Pancreatic Islets..................115 Gladys Teitelman and Irem Nasir 7 Transcription Factor-Directed Differentiation of Stem Cells Along an Endocrine Lineage .................133 William L. Lowe, Jr. 8 Generation of Islet-Like Structures From ES Cells...........147 Nadya Lumelsky 9 The Therapeutic Potential of Liver Repopulation for Metabolic or Endocrine Disorders..........................165 Sanjeev Gupta xi

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