Expression of mRNAs for pore-forming protein and two serine esterases in murine primary and cloned effector lymphocytes

J Cell Biochem. 1990 May;43(1):81-8. doi: 10.1002/jcb.240430108.

Abstract

The cDNAs encoding several proteins present in the granules of cytolytic effector lymphocytes have now been cloned. These include the cytolytic pore-forming protein (PFP) or perforin, and at least six serine esterases (SE), also called granzymes. The cDNA probes for PFP, SE-1, and SE-2 are used here to study the expression of these proteins in murine primary effector lymphocytes. Among the stimuli effective in inducing the expression of PFP, SE-1, and SE-2 were recombinant interleukin-2, the lectin concanavalin A in the presence of phorbol esters, and allogeneic cells in mixed lymphocyte cultures. Some correlation was seen between the levels of PFP and SE mRNAs and cytotoxicity measured in a standard 51Cr release assay. We also examined a panel of 13 cloned cytotoxic T lymphocyte (CTL) lines and found that mRNAs for PFP and SE-2 were expressed in all CTL lines, including some that were previously considered not to produce PFP. Twelve of the 13 CTL lines also proved to possess the mRNA for SE-1. One thymoma cell line, TIMI.4, did not express mRNA for PFP, although it expressed mRNA for SE-1 and SE-2.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Northern
  • Cell Line
  • Cells, Cultured
  • Clone Cells
  • Esterases / genetics*
  • Lymphocyte Activation
  • Membrane Glycoproteins*
  • Membrane Proteins / genetics*
  • Mice
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • RNA, Messenger / biosynthesis*
  • T-Lymphocytes, Cytotoxic / metabolism*

Substances

  • Membrane Glycoproteins
  • Membrane Proteins
  • Pore Forming Cytotoxic Proteins
  • RNA, Messenger
  • Perforin
  • Esterases
  • serine esterase