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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1985-3-20
pubmed:abstractText
The phenotype of B lineage cells (TdT+, pre-B, IgM+, IgD-, and IgM+,IgD+) in infant and adult human bone marrow was compared with that of B cells seen in peripheral tissues such as tonsil and blood. The range of B cell-associated antibodies used included four reagents with greater than 90% reactivity on peripheral B cells: RFB4 and To15 (both p135, corresponding to CD22), RFB6 (p140 corresponding to CD21), and Y29/55, a unique B cell-specific antibody. In addition, AL-1, an antibody with virtually no reactivity against peripheral B cells was also used. The BM cell subpopulations were heterogeneous in respect of antibody reactivity. The TdT+, pre-B and IgM+, IgD- cells were AL-1+ but did not express membrane antigens recognized by the antibodies To15, RFB4 (CD22), and RFB6 (CD21). TdT+, pre-B cells, and 50% of IgM+, IgD- BM B cells were also unreactive with antibody Y29/55, the other 50% being Y29/55+. In contrast, the IgM+,IgD+ BM B cells, like peripheral B cells, were positive with antibodies To15, RFB4, RFB6, and Y29/55, but reacted only in small numbers with AL-1. The orderly differentiation-linked display of these antigens was also suggested by the findings that normal TdT+, pre-B, and IgM+,IgD- cells expressed the To15 and RFB4 (CD22) antigens in their cytoplasm (in the Golgi region). This observation was confirmed in malignant common acute lymphoblastic and pre-B blast cells, as well as in the corresponding permanent cell lines KM3 and NALM-6. In these lines the membrane expression of To15 and RFB4 could be induced by phorbol ester during a 48 to 72 hr culture period.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:volume
134
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1524-30
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:3918103-Adolescent, pubmed-meshheading:3918103-Adult, pubmed-meshheading:3918103-Animals, pubmed-meshheading:3918103-Antibodies, Monoclonal, pubmed-meshheading:3918103-Antigens, Differentiation, B-Lymphocyte, pubmed-meshheading:3918103-Antigens, Surface, pubmed-meshheading:3918103-B-Lymphocytes, pubmed-meshheading:3918103-Bone Marrow, pubmed-meshheading:3918103-Bone Marrow Cells, pubmed-meshheading:3918103-Cell Line, pubmed-meshheading:3918103-Child, pubmed-meshheading:3918103-Child, Preschool, pubmed-meshheading:3918103-Cytoplasm, pubmed-meshheading:3918103-Goats, pubmed-meshheading:3918103-Humans, pubmed-meshheading:3918103-Leukemia, Lymphoid, pubmed-meshheading:3918103-Lymphoid Tissue, pubmed-meshheading:3918103-Palatine Tonsil, pubmed-meshheading:3918103-Regeneration
pubmed:year
1985
pubmed:articleTitle
Human B cell development. I. Phenotypic differences of B lymphocytes in the bone marrow and peripheral lymphoid tissue.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't