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PMID: 6603621 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Long-term growth of human B cells and their use in a microassay for B-cell growth factor.

Maizel AL, Morgan JW, Mehta SR, Kouttab NM, Bator JM, Sahasrabuddhe CG

Abstract

Normal human B lymphocytes, prepared from peripheral venous blood, have been stimulated with intact anti-IgM (mu chain specific) bound to an insoluble matrix. The activation event, in a subfraction of human B cells, was associated with subsequent receptivity to the mitogenic effects of exogenously added B-cell growth factor. The ability of the cell population to specifically absorb the B-cell growth factor was dependent upon the time of stimulation with the anti-IgM. Continuous replenishment of the growth factor resulted in the ability to maintain long-term growth-factor-dependent human B-cell populations. These cultured B lymphocytes were shown to specifically absorb the B-cell growth factor, suggesting the presence of membrane receptors for it. The cultured B lymphocytes were routinely maintained in logarithmic-phase growth, in the presence of growth factor, with a population doubling time of 36 hr. These cultured B cells have been utilized in a microassay for the assessment of B-cell growth factor activity that is accurate, sensitive, and precise.

MeSH Terms
B-Lymphocytes/drug effects,immunology Biological Assay DNA Replication/drug effects Humans Lymphocyte Activation Lymphokines/analysis,pharmacology T-Lymphocytes/immunology Thymidine/metabolism Tritium
Chemicals
Lymphokines Tritium Thymidine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Maizel A L
Morgan J W
Mehta S R
Kouttab N M
Bator J M
Sahasrabuddhe C G
References (19)
19 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-08-00
Pages
5047-51
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC384185
Subset
IM
Grants
NCI NIH HHS · CA21927 · United States
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