Molecular mechanisms of lymphocyte-mediated killing.

J. D. Young*, C. C. Liu, P. M. Persechini

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Lymphocytes kill tumor cells and other target cells by a contact-dependent mechanism. Killer lymphocytes acquire cytoplasmic granules upon lymphokine stimulation and these granules in turn contain potent cytotoxic mediators, some of which have been characterized recently. These include (i) a pore-forming protein (perforin) of 70 kDa that polymerizes into transmembrane tubules in the presence of calcium and that is structurally related to the terminal components (C5b-6, C7, C8 and C9) of the complement cascade, (ii) a cytokine related to tumor necrosis factor and lymphotoxin that causes DNA fragmentation in target cells, and (iii) a family of serine esterases presently without any known function. The relevance of these mediators in lymphocyte-mediated killing is currently being investigated. The identification and characterization of additional putative mediators of cytotoxicity in the future will undoubtedly provide us with a better understanding of the molecular basis of cell-mediated killing.

Original languageEnglish
Pages (from-to)1145-1153
Number of pages9
JournalBrazilian Journal of Medical and Biological Research
Volume21
Issue number6
StatePublished - 1988
Externally publishedYes

Keywords

  • Antibody-Dependent Cell Cytotoxicity
  • Cell Membrane Permeability
  • Complement
  • Complement Membrane Attack Complex
  • Killer Cells, Natural
  • Major Histocompatibility Complex
  • Membrane Proteins
  • Support, Non-U.S. Gov't
  • Support, U.S. Gov't, P.H.S.
  • T-Lymphocytes, Cytotoxic

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