HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) Supplemental Data All Versions of this Article: 2006-0217v1 24/12/2703    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints/Permissions Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Pelayo, R. Articles by Kincade, P. W. Search for Related Content PubMed PubMed Citation Articles by Pelayo, R. Articles by Kincade, P. W.

THE STEM CELL NICHE

Cell Cycle Quiescence of Early Lymphoid Progenitors in Adult Bone Marrow

^aImmunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA;
^bDepartment of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada

Key Words. Adult stem cells • B lymphopoiesis • Fetal stem cells • G₀ • Hematopoiesis • Hematopoietic cell transplantation Hematopoietic progenitor cells • Hematopoietic stem cell

Correspondence: Paul W. Kincade, Ph.D., 825 NE 13th Street, Oklahoma City, Oklahoma 73104, USA. Telephone: 405-271-7905; Fax: 405-271-8568; e-mail: kincade{at}omrf.ouhsc.edu

Received April 12, 2006; accepted for publication August 15, 2006.
First published online in STEM CELLS EXPRESS   August 24, 2006.



Lymphocyte production in bone marrow (BM) requires substantial cell division, but the relationship between largely quiescent stem cells and dividing lymphoid progenitors is poorly understood. Therefore, the proliferation and cell cycle status of murine hematopoietic progenitors that have just initiated the lymphoid differentiation program represented the focus of this study. Continuous bromo-2'-deoxyuridine (BrdU) incorporation and DNA/RNA analysis by flow cytometry revealed that a surprisingly large fraction of RAG-1⁺c-kit^hi early lymphoid progenitors (ELPs) and RAG-1⁺c-kit^lo pro-lymphocytes (Pro-Ls) in adult BM were in cell cycle quiescence. In contrast, their counterparts in 14-day fetal liver actively proliferated. Indeed, the growth fraction (cells in G₁-S-G₂-M phases) of fetal ELPs was on average 80% versus only 30% for adult ELPs. After 5-fluorouracil treatment, as many as 60% of the adult ELP-enriched population was in G₁-S-G₂-M and 34% incorporated BrdU in 6 hours. Transcripts for Bcl-2, p21Cip1/Waf1, and p27 Kip1 cell cycle regulatory genes correlated inversely well with proliferative activity. Interestingly, adult lymphoid progenitors in rebound had the high potential for B lymphopoiesis in culture typical of their fetal counterparts. Thus, lymphocyte production is sustained during adult life by quiescent primitive progenitors that divide intermittently. Some, but not all, aspects of the fetal differentiation program are reacquired after chemotherapy.