Induction of CD5 on B and T cells is suppressed by cyclosporin A, FK-520 and rapamycin

Int Immunol. 1995 Mar;7(3):381-92. doi: 10.1093/intimm/7.3.381.

Abstract

The expression of CD5 can be induced on murine B-2 cells by anti-IgM, a recognized analog of thymus-independent 2 type (TI-2) antigen. Given that cyclosporin A (CsA) sensitivity is a distinguishing feature of TI-2 type B cell activation, we asked whether the in vitro induction of CD5 on B cells by anti-mu is CsA sensitive. We report that anti-mu induced CD5 expression on B-2 cells was inhibited by CsA as well as FK-520 and rapamycin. When L-685,818, a FK-520 and rapamycin antagonist, was added to anti-mu stimulated B cell cultures containing FK-520 or rapamycin, but not CsA, suppression was abrogated and complete induction of CD5 was seen. When we used either CD4+CD8+ thymocytes or peripheral T cells activated by phorbol ester and ionomycin, the cell surface induction of CD5 was also partially blocked by CsA, FK-520 and rapamycin. Moreover, in both B and T cells, the same immunosuppressive drugs did not affect constitutive CD5 expression but only blocked de novo induction. To determine the level of CD5 regulation, we activated T cells using phorbol myristate acetate (PMA)/ionomycin and report that CD5 induction was sensitive to actinomycin D (AcD). Similarly, the induction of CD5 on anti-mu activated B cells was blocked by AcD. In addition, T cells that were activated by PMA/ionomycin expressed more abundant CD5 mRNA than CsA or FK-520 treated cells. Based on the CsA-sensitive regulation of CD5 we thought that the CsA-sensitive nuclear factor of activated T cells (NFAT) might be involved in CD5 regulation. We report evidence by Western blot analysis that NFATp is expressed by both resting and TI activated B cells but apparently not CD4+CD8+CD5+ thymocytes. We conclude that in both B and T cells the induction of CD5 requires transcriptional regulation, and that the inhibition of CD5 expression by the immunosuppressive drugs CsA, FK-520 and rapamycin requires drug-immunophilin complex formation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Anti-Idiotypic / pharmacology
  • Antigens, CD / biosynthesis*
  • Antigens, CD / genetics
  • Autoimmunity
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / metabolism
  • CD5 Antigens
  • Carrier Proteins / metabolism
  • Cell Cycle
  • Cyclosporine / pharmacology*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology
  • Gene Expression Regulation / drug effects*
  • Heat-Shock Proteins / metabolism
  • Ionomycin / pharmacology
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred CBA
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Polyenes / antagonists & inhibitors
  • Polyenes / pharmacology*
  • Sirolimus
  • T-Lymphocyte Subsets / drug effects*
  • T-Lymphocyte Subsets / metabolism
  • Tacrolimus / analogs & derivatives*
  • Tacrolimus / antagonists & inhibitors
  • Tacrolimus / pharmacology
  • Tacrolimus Binding Proteins
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription Factors / biosynthesis
  • Transcription Factors / physiology
  • Transcription, Genetic

Substances

  • Antibodies, Anti-Idiotypic
  • Antigens, CD
  • CD5 Antigens
  • Carrier Proteins
  • DNA-Binding Proteins
  • Heat-Shock Proteins
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Polyenes
  • Transcription Factors
  • anti-IgM
  • L 685818
  • Ionomycin
  • Cyclosporine
  • immunomycin
  • Tacrolimus Binding Proteins
  • Tetradecanoylphorbol Acetate
  • Sirolimus
  • Tacrolimus