Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (35)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kirman, I.
Right arrow Articles by Weksler, M. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kirman, I.
Right arrow Articles by Weksler, M. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

International Immunology, Vol 10, 1385-1392, Copyright © 1998 by Oxford University Press


ARTICLES

Increased apoptosis of bone marrow pre-B cells in old mice associated with their low number

I Kirman, K Zhao, Y Wang, P Szabo, W Telford and ME Weksler
Division of Geriatrics and Gerontology, Cornell University Medical College, New York, NY 10021, USA.

The number of bone marrow pre-B cells is significantly lower in 18- than in 2-month-old BALB/c mice. The percentage of apoptotic pre-B cells, freshly isolated or cultured, from 18-month-old mice was significantly greater than from 2-month-old mice. The increased percentage of apoptotic pre-B cells from old mice was associated with a decreased level of bcl-xL mRNA, detected by RT-PCR, and of Bcl-xL protein, detected by intracellular staining. Consistent with an age- associated increase in apoptosis in pre-B cells was the fact that significantly fewer pre-B cells were generated after in vitro cultures of pro-B cells from old as compared to young mice. Furthermore, fewer pre-B cells survived and fewer sIg-expressing B cells were generated in cultures of pre-B cells from old as compared to young mice. In addition, there was no detectable difference in the secretion of IL-7 by bone marrow cells from 2- or 18-month-old mice. Thus, increased apoptosis of bone marrow pre-B cells in old mice appears to contribute to their decreased number.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Immunol.Home page
J. A. Dudakov, G. L. Goldberg, J. J. Reiseger, K. Vlahos, A. P. Chidgey, and R. L. Boyd
Sex Steroid Ablation Enhances Hematopoietic Recovery following Cytotoxic Antineoplastic Therapy in Aged Mice
J. Immunol., December 1, 2009; 183(11): 7084 - 7094.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. A. Dudakov, G. L. Goldberg, J. J. Reiseger, A. P. Chidgey, and R. L. Boyd
Withdrawal of Sex Steroids Reverses Age- and Chemotherapy-Related Defects in Bone Marrow Lymphopoiesis
J. Immunol., May 15, 2009; 182(10): 6247 - 6260.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
C. Gekas, K. E. Rhodes, L. M. Gereige, H. Helgadottir, R. Ferrari, S. K. Kurdistani, E. Montecino-Rodriguez, R. Bassel-Duby, E. Olson, A. V. Krivtsov, et al.
Mef2C is a lineage-restricted target of Scl/Tal1 and regulates megakaryopoiesis and B-cell homeostasis
Blood, April 9, 2009; 113(15): 3461 - 3471.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
S. Alter-Wolf, B. B. Blomberg, and R. L. Riley
Deviation of the B Cell Pathway in Senescent Mice Is Associated with Reduced Surrogate Light Chain Expression and Altered Immature B Cell Generation, Phenotype, and Light Chain Expression
J. Immunol., January 1, 2009; 182(1): 138 - 147.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
A. M. King, E. Van der Put, B. B. Blomberg, and R. L. Riley
Accelerated Notch-Dependent Degradation of E47 Proteins in Aged B Cell Precursors Is Associated with Increased ERK MAPK Activation
J. Immunol., March 15, 2007; 178(6): 3521 - 3529.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
H. Min, E. Montecino-Rodriguez, and K. Dorshkind
Effects of Aging on the Common Lymphoid Progenitor to Pro-B Cell Transition
J. Immunol., January 15, 2006; 176(2): 1007 - 1012.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
G. Shahaf, K. Johnson, and R. Mehr
B cell development in aging mice: lessons from mathematical modeling
Int. Immunol., January 1, 2006; 18(1): 31 - 39.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
E. Van der Put, D. Frasca, A. M. King, B. B. Blomberg, and R. L. Riley
Decreased E47 in Senescent B Cell Precursors Is Stage Specific and Regulated Posttranslationally by Protein Turnover
J. Immunol., July 15, 2004; 173(2): 818 - 827.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
M. I. D. Rossi, T. Yokota, K. L. Medina, K. P. Garrett, P. C. Comp, A. H. Schipul Jr, and P. W. Kincade
B lymphopoiesis is active throughout human life, but there are developmental age-related changes
Blood, January 15, 2003; 101(2): 576 - 584.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
K. M. Johnson, K. Owen, and P. L. Witte
Aging and developmental transitions in the B cell lineage
Int. Immunol., November 1, 2002; 14(11): 1313 - 1323.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
S. Okada, T. Yoshida, Z. Hong, G. Ishii, M. Hatano, M. Kuro-o, Y. Nabeshima, Y.-i. Nabeshima, and T. Tokuhisa
Impairment of B lymphopoiesis in precocious aging (klotho) mice
Int. Immunol., June 1, 2000; 12(6): 861 - 871.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.