TY - JOUR
T1 - Direct demonstration of MHC class II surface expression on murine pre-B cells
AU - Tarlinton, David
PY - 1993/12/1
Y1 - 1993/12/1
N2 - Using multi-parameter flow cytometry, MHC class II (Ia) antigens were found to be expressed at readily detectable levels on the majority of surface IgM- B lineage cells in the bone marrow of adult mice. Approximately 90% of the pre-B cells (B220+IgM-) in BALB/c bone marrow (BM) were MCH class II positive, while in C57BL/6 this figure was somewhat less, ̃60%. Analysis of adult BM for the correlated expression of Ia both with heat stable antigen (HSA) and BP-1 on B lineage cells revealed in both cases a small fraction of cells expressing either the HSA or BP-1 but lacking Ia. This result suggests that the onset of expression of both HSA and BP-1 precede that of Ia in B cell development. When the B22010CD43+ pro-B cell compartment from BALB/c BM was analysed for the expression of Ia very few, if any, cells were found to be positive. Of the remaining B220+ cells, >90% express detectable Ia. Thus the onset of Ia expression would appear to be soon after the pro-B cell compartment. The results presented here resolve the previous discrepancy between human and murine pre-B cell differentiation of when Ia is first expressed, and additionally, by identifying a new pre-B cell antigen, allow for the refinement of existing schemes of murine B cell development.
AB - Using multi-parameter flow cytometry, MHC class II (Ia) antigens were found to be expressed at readily detectable levels on the majority of surface IgM- B lineage cells in the bone marrow of adult mice. Approximately 90% of the pre-B cells (B220+IgM-) in BALB/c bone marrow (BM) were MCH class II positive, while in C57BL/6 this figure was somewhat less, ̃60%. Analysis of adult BM for the correlated expression of Ia both with heat stable antigen (HSA) and BP-1 on B lineage cells revealed in both cases a small fraction of cells expressing either the HSA or BP-1 but lacking Ia. This result suggests that the onset of expression of both HSA and BP-1 precede that of Ia in B cell development. When the B22010CD43+ pro-B cell compartment from BALB/c BM was analysed for the expression of Ia very few, if any, cells were found to be positive. Of the remaining B220+ cells, >90% express detectable Ia. Thus the onset of Ia expression would appear to be soon after the pro-B cell compartment. The results presented here resolve the previous discrepancy between human and murine pre-B cell differentiation of when Ia is first expressed, and additionally, by identifying a new pre-B cell antigen, allow for the refinement of existing schemes of murine B cell development.
KW - B cell development
KW - Ia expression
KW - Pro-B cell
UR - http://www.scopus.com/inward/record.url?scp=0027752061&partnerID=8YFLogxK
U2 - 10.1093/intimm/5.12.1629
DO - 10.1093/intimm/5.12.1629
M3 - Article
C2 - 8312232
AN - SCOPUS:0027752061
VL - 5
SP - 1629
EP - 1635
JO - International Immunology
JF - International Immunology
SN - 0953-8178
IS - 12
ER -