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KINETICS OF PERITONEAL B-1A CELLS (CD5 B-CELLS) IN YOUNG-ADULT MICE
DEENEN, GJ. & KROESE, FGM., Jan-1993, In : European Journal of Immunology. 23, 1, p. 12-16 5 p.Research output: Contribution to journal › Article › Academic › peer-review
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KINETICS OF PERITONEAL B-1A CELLS (CD5 B-CELLS) IN YOUNG-ADULT MICE. / DEENEN, GJ; KROESE, FGM.
In: European Journal of Immunology, Vol. 23, No. 1, 01.1993, p. 12-16.Research output: Contribution to journal › Article › Academic › peer-review
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TY - JOUR
T1 - KINETICS OF PERITONEAL B-1A CELLS (CD5 B-CELLS) IN YOUNG-ADULT MICE
AU - DEENEN, GJ
AU - KROESE, FGM
PY - 1993/1
Y1 - 1993/1
N2 - In the mouse, conventional B cells are continuously generated from precursor cells located in the bone marrow (BM), whereas the small subset of B-1 cells (formerly called Ly-1 B cells) constitute a self-replenishing population of cells. Here we studied the kinetics of murine peritoneal B-1a cells (i.e. B-1 cells expressing CD5). The actual number of B-1a cells in the peritoneal cavity that are proliferating, as detected by metaphase arrest and S-phase index, was below detection level, indicating that these cells do not divide significantly at this anatomical location. To establish the life-span of B-1a cells we used long-term administration of 5-bromo-2'-deoxyuridine in combination with three-color immunocytology on cytospin preparations. The renewal rate of peritoneal B-1a cells was 1.3% per day representing a 50% renewal time of 38 days. Splenic B cells and popliteal lymph node B cells (predominantly conventional B cells) showed an almost identical renewal rate of 1.1 % per day. The data show that peripheral B cells from various lymphoid tissues and locations do not differ significantly in their renewal capacity, even though there are differences in their developmental origin.
AB - In the mouse, conventional B cells are continuously generated from precursor cells located in the bone marrow (BM), whereas the small subset of B-1 cells (formerly called Ly-1 B cells) constitute a self-replenishing population of cells. Here we studied the kinetics of murine peritoneal B-1a cells (i.e. B-1 cells expressing CD5). The actual number of B-1a cells in the peritoneal cavity that are proliferating, as detected by metaphase arrest and S-phase index, was below detection level, indicating that these cells do not divide significantly at this anatomical location. To establish the life-span of B-1a cells we used long-term administration of 5-bromo-2'-deoxyuridine in combination with three-color immunocytology on cytospin preparations. The renewal rate of peritoneal B-1a cells was 1.3% per day representing a 50% renewal time of 38 days. Splenic B cells and popliteal lymph node B cells (predominantly conventional B cells) showed an almost identical renewal rate of 1.1 % per day. The data show that peripheral B cells from various lymphoid tissues and locations do not differ significantly in their renewal capacity, even though there are differences in their developmental origin.
KW - B-1 CELLS
KW - KINETICS
KW - IMMUNOCYTOLOGY
KW - BROMODEOXYURIDINE
KW - PERIPHERAL LYMPHOID ORGANS
KW - BONE-MARROW
KW - LY-1 B
KW - POPULATION-KINETICS
KW - MURINE-B
KW - LYMPHOCYTES
KW - MOUSE
KW - BROMODEOXYURIDINE
KW - PROLIFERATION
KW - EXPRESSION
M3 - Article
VL - 23
SP - 12
EP - 16
JO - European Journal of Immunology
JF - European Journal of Immunology
SN - 0014-2980
IS - 1
ER -
ID: 6339559