Several previously described B cell growth factor (BCGF) activities from a number of mouse monoclonal T cell sources were compared in different functional assays. The results indicate that there are two distinct classes of BCGF defined by functional activity and source. BCGF I, whose prototype is (EL4)BCGF, synergized with anti-Ig in the proliferation of normal splenic B cells but had no activity when dextran sulfate (DXS), rather than anti-Ig, was used to costimulate the same source of B cells. BCGF I also failed to directly stimulate BCL1 tumor B cells. In contrast, BCGF II, whose prototype is (DL)BCGF, showed a reciprocal pattern of activity. BCGF II failed to synergize with anti-Ig-costimulated normal B cells to give good proliferative responses. Sources of BCGF II also directly stimulated (no anti-Ig or DXS added) B cells of the BCL1 tumor-carrying mice. These results suggest that the two BCGF may have activity on two subsets of B cells that respond differentially to induction with the two polyclonal B cell activators, anti-Ig and DXS. The possibilities that these different patterns of response occur in separate lineages of B cells and/or in B cells in different states of differentiation is discussed.
Skip Nav Destination
Article navigation
1 September 1983
Article|
September 01 1983
Evidence for two distinct classes of murine B cell growth factors with activities in different functional assays.
S L Swain
M Howard
J Kappler
P Marrack
J Watson
R Booth
G D Wetzel
R W Dutton
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1983) 158 (3): 822–835.
Citation
S L Swain, M Howard, J Kappler, P Marrack, J Watson, R Booth, G D Wetzel, R W Dutton; Evidence for two distinct classes of murine B cell growth factors with activities in different functional assays.. J Exp Med 1 September 1983; 158 (3): 822–835. doi: https://doi.org/10.1084/jem.158.3.822
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement