Age-related changes of human bone marrow: a histometric estimation of proliferative cells, apoptotic cells, T cells, B cells and macrophages

2000 ◽  
Vol 117 (1-3) ◽  
pp. 57-68 ◽  
Author(s):  
Takafumi Ogawa ◽  
Masanobu Kitagawa ◽  
Katsuiku Hirokawa
Cytometry ◽  
2004 ◽  
Vol 60B (1) ◽  
pp. 1-13 ◽  
Author(s):  
E.G. van Lochem ◽  
V.H.J. van der Velden ◽  
H.K. Wind ◽  
J.G. te Marvelde ◽  
N.A.C. Westerdaal ◽  
...  

Blood ◽  
1976 ◽  
Vol 47 (3) ◽  
pp. 423-430 ◽  
Author(s):  
NL Abdou ◽  
JB Alavi ◽  
NI Abdou

Characterization of the different lymphocyte populations in normal human bone marrow (BM) was attempted and compared to that in the peripheral blood (PB). B cells comprised 34% +/- 11% of lymphocytes in BM and 23% +/- 9% in PB. The majority of B cells carried IgM in BM and IgG in the PB. In the BM, cells carrying complement or Fc receptors were fewer than cells carrying Ig, but in the PB they were equal. T cells comprised 6% +/- 4% of lymphocytes in the BM and 62% +/- 7% in the PB. The majority of BM lymphocytes did not have B or T cell markers; these probably included B and T cell precursors. BM lymphocytes carrying surface Ig increased in a 7-day culture, whereas those of the PB decreased. Pokeweed mitogen induced Ig synthesis in B cells of PB but not those of BM. BM-T cells were more efficient than PB- T cells in inhibiting Ig synthesis of PB-B cells. These results indicate that the BM compartment contains immature B cells that are capable of partial differentiation and maturation in vitro. BM-B lymphocytes are probably not involved in the effector phase of the immune response since they are unable to synthesize Ig and because they carry few receptors for complement of Fc, BM-T lymphocytes are very few and have suppressor capability and therefore may play an essential role in regulation of Ig synthesis by B cells.


Blood ◽  
1976 ◽  
Vol 47 (3) ◽  
pp. 423-430 ◽  
Author(s):  
NL Abdou ◽  
JB Alavi ◽  
NI Abdou

Abstract Characterization of the different lymphocyte populations in normal human bone marrow (BM) was attempted and compared to that in the peripheral blood (PB). B cells comprised 34% +/- 11% of lymphocytes in BM and 23% +/- 9% in PB. The majority of B cells carried IgM in BM and IgG in the PB. In the BM, cells carrying complement or Fc receptors were fewer than cells carrying Ig, but in the PB they were equal. T cells comprised 6% +/- 4% of lymphocytes in the BM and 62% +/- 7% in the PB. The majority of BM lymphocytes did not have B or T cell markers; these probably included B and T cell precursors. BM lymphocytes carrying surface Ig increased in a 7-day culture, whereas those of the PB decreased. Pokeweed mitogen induced Ig synthesis in B cells of PB but not those of BM. BM-T cells were more efficient than PB- T cells in inhibiting Ig synthesis of PB-B cells. These results indicate that the BM compartment contains immature B cells that are capable of partial differentiation and maturation in vitro. BM-B lymphocytes are probably not involved in the effector phase of the immune response since they are unable to synthesize Ig and because they carry few receptors for complement of Fc, BM-T lymphocytes are very few and have suppressor capability and therefore may play an essential role in regulation of Ig synthesis by B cells.


2018 ◽  
Vol 141 (5) ◽  
pp. 1911-1913.e7 ◽  
Author(s):  
Sonya C. Becker ◽  
Martin Szyska ◽  
Angela Mensen ◽  
Katharina Hellwig ◽  
Raik Otto ◽  
...  

Cryobiology ◽  
1994 ◽  
Vol 31 (5) ◽  
pp. 478-482
Author(s):  
Zhong-Xing Zhang ◽  
Yuan-Ji Xu ◽  
Yuen Chen ◽  
Yan Li ◽  
Bei-Fen Shen ◽  
...  

Blood ◽  
2011 ◽  
Vol 117 (11) ◽  
pp. 3104-3112 ◽  
Author(s):  
Zohar Keren ◽  
Shulamit Naor ◽  
Shahar Nussbaum ◽  
Karin Golan ◽  
Tomer Itkin ◽  
...  

Abstract Aging is associated with a decline in B-lymphopoiesis in the bone marrow and accumulation of long-lived B cells in the periphery. These changes decrease the body's ability to mount protective antibody responses. We show here that age-related changes in the B lineage are mediated by the accumulating long-lived B cells. Thus, depletion of B cells in old mice was followed by expansion of multipotent primitive progenitors and common lymphoid progenitors, a revival of B-lymphopoiesis in the bone marrow, and generation of a rejuvenated peripheral compartment that enhanced the animal's immune responsiveness to antigenic stimulation. Collectively, our results suggest that immunosenescence in the B-lineage is not irreversible and that depletion of the long-lived B cells in old mice rejuvenates the B-lineage and enhances immune competence.


2006 ◽  
Vol 177 (10) ◽  
pp. 6730-6737 ◽  
Author(s):  
Xiaoyu Zhang ◽  
Haidong Dong ◽  
Wei Lin ◽  
Stephen Voss ◽  
Lucinda Hinkley ◽  
...  

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