Regulation of Cell Proliferation and Differentiation

  • Warren W. Nichols
  • Donald G. Murphy

Part of the Cellular Senescence and Somatic Cell Genetics book series (CSSCG)

Table of contents

  1. Front Matter
    Pages i-xii
  2. Clinical Overgrowth, Undergrowth, and Failure to Thrive

  3. Cellular Regulation in Cell Proliferation In vitro

    1. H. Holtzer, G. Yeoh, N. Rubinstein, J. Chi, S. Fellini, S. Dienstman
      Pages 87-104
    2. Irwin R. Konigsberg
      Pages 105-137
    3. Mark Nameroff
      Pages 139-142
  4. Molecular Studies in Regulation of Cell Proliferation

  5. Back Matter
    Pages 197-204

About this book

Introduction

In 1974 The National Institute on Aging established a somatic cell genetic resource for aging research at the Institute for Medical Research in Camden, New Jersey. Within this program there is a yearly workshop to promote theory and concept develop­ ment in aging research with the specific purpose of addressing the use of genetically marked cells for aging research and to stimulate interest in aging research by workers in a variety of disciplines. This monograph, The Regulation of Cell Proliferation and Differentiation, is the result of the first workshop held May 15-17, 1975. The concept of the workshop was to consider two main areas: First, a discussion of clinical syndromes expressing as a major manifestation excessive growth, deficient growth or failure to thrive; and second, to present work in cellular and molecular biology on a model system suitable for in vitro study of regulation of cell proliferation and diff2rentiation. The model selected for this was skeletal muscle. It has been widely accepted that normal somatic cells from individual human donors display limited replicative lifespans when cultivated in vitro (1,2). That such "clonal senescence" may be related to in vivo aging is suggested by observations relating the replicative lifespans of cultures to donor age (3-5,13) donor genotype (4-7) and donor's tissue of origin (5,8). A variety of theories have been developed to explain in vitro clonal senescence (9).

Keywords

age aging biology cell cells growth molecular biology muscle proliferation regulation research senescence skeletal muscle syndromes tissue

Editors and affiliations

  • Warren W. Nichols
    • 1
  • Donald G. Murphy
    • 2
  1. 1.Institute for Medical ResearchCamdenUSA
  2. 2.National Institute on AgingBethesdaUSA

Bibliographic information

  • DOI https://doi.org/10.1007/978-1-4615-8846-7
  • Copyright Information Springer-Verlag US 1977
  • Publisher Name Springer, Boston, MA
  • eBook Packages Springer Book Archive
  • Print ISBN 978-1-4615-8848-1
  • Online ISBN 978-1-4615-8846-7
  • About this book