The JI PBL Intereron Source
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zharhary, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zharhary, D.

The Journal of Immunology, Vol 141, Issue 6 1863-1869, Copyright © 1988 by American Association of Immunologists


ARTICLES

Age-related changes in the capability of the bone marrow to generate B cells

D Zharhary
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

The capability of the bone marrow (BM) to generate new B cells in aging was studied in vitro. BM cells from old (26 to 30 mo) or young (3 mo) BALB/c and (C3H/eB x C57BL/6)F1 mice were depleted of mature B cells and these surface Ig (sIg) BM cells were incubated in culture for 3 days. The frequency of newly generated B cells in these cultures was determined by assessing the frequency of slg+ cells and of B cells forming colonies in agar and by assaying the proliferative capacity of these newly generated B cells after stimulation by LPS. We found that BM cells from aged mice are significantly inferior to young ones in their capability to generate new B cells in culture. By mixing old and young slg- BM cells, we found that, in general, this reduction was not caused by a suppressive effect of T cells or of any other cells, but rather to lack of some sort of supportive cell or factor in the aged BM. In addition, we found that the frequency of cells expressing the B220 surface molecule, a B lineage-specific marker, is significantly reduced in aged BM. These results indicate that a quantitative decrease in B cell progenitors combined with changes in cell populations that are important in supporting B cell generation contribute to the age- related decrease in the capacity to generate B cells.


This article has been cited by other articles:


Home page
J. Immunol.Home page
D. Frasca, A. M. Landin, R. L. Riley, and B. B. Blomberg
Mechanisms for Decreased Function of B Cells in Aged Mice and Humans
J. Immunol., March 1, 2008; 180(5): 2741 - 2746.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
I. Tsuboi, K. Morimoto, Y. Hirabayashi, G.-X. Li, S. Aizawa, K. J. Mori, J. Kanno, and T. Inoue
Senescent B Lymphopoiesis Is Balanced in Suppressive Homeostasis: Decrease in Interleukin-7 and Transforming Growth Factor-{beta} Levels in Stromal Cells of Senescence-Accelerated Mice
Experimental Biology and Medicine, June 1, 2004; 229(6): 494 - 502.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
P. Ghia, G. Prato, C. Scielzo, S. Stella, M. Geuna, G. Guida, and F. Caligaris-Cappio
Monoclonal CD5+ and CD5- B-lymphocyte expansions are frequent in the peripheral blood of the elderly
Blood, March 15, 2004; 103(6): 2337 - 2342.
[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
J. Immunol.Home page
S. A. Johnson, S. J. Rozzo, and J. C. Cambier
Aging-Dependent Exclusion of Antigen-Inexperienced Cells from the Peripheral B Cell Repertoire
J. Immunol., May 15, 2002; 168(10): 5014 - 5023.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
N. Manabe, H. Kawaguchi, H. Chikuda, C. Miyaura, M. Inada, R. Nagai, Y.-i. Nabeshima, K. Nakamura, A. M. Sinclair, R. H. Scheuermann, et al.
Connection Between B Lymphocyte and Osteoclast Differentiation Pathways
J. Immunol., September 1, 2001; 167(5): 2625 - 2631.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
A. S. Eaton-Bassiri, L. Mandik-Nayak, S.-j. Seo, M. P. Madaio, M. P. Cancro, and J. Erikson
Alterations in splenic architecture and the localization of anti-double-stranded DNA B cells in aged mice
Int. Immunol., June 1, 2000; 12(6): 915 - 926.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. LeMaoult, J. S. Manavalan, R. Dyall, P. Szabo, J. Nikolic-Zugic, and M. E. Weksler
Cellular Basis of B Cell Clonal Populations in Old Mice
J. Immunol., June 1, 1999; 162(11): 6384 - 6391.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
G. H. Kline, T. A. Hayden, and N. R. Klinman
B Cell Maintenance in Aged Mice Reflects Both Increased B Cell Longevity and Decreased B Cell Generation
J. Immunol., March 15, 1999; 162(6): 3342 - 3349.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
K. M. Moscatello, K. L. Biber, D. C. Dempsey, R. Chervenak, and R. M. Wolcott
Characterization of a B Cell Progenitor Present in Neonatal Bone Marrow and Spleen But Not in Adult Bone Marrow and Spleen
J. Immunol., November 15, 1998; 161(10): 5391 - 5398.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
E. M. Sherwood, B. B. Blomberg, W. Xu, C. A. Warner, and R. L. Riley
Cutting Edge: Senescent BALB/c Mice Exhibit Decreased Expression of {lambda}5 Surrogate Light Chains and Reduced Development Within the Pre-B Cell Compartment
J. Immunol., November 1, 1998; 161(9): 4472 - 4475.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
R. P. Stephan, C. R. Reilly, and P. L. Witte
Impaired Ability of Bone Marrow Stromal Cells to Support B-Lymphopoiesis With Age
Blood, January 1, 1998; 91(1): 75 - 88.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.