Differential VIP and VIP1 receptor gene expression in rat thymocyte subsets

Peptides. 1996;17(5):803-7. doi: 10.1016/0196-9781(96)00070-8.

Abstract

Nervous, endocrine, and immune systems share a large number of regulatory molecules including hormones and neuropeptides. Vasoactive intestinal peptide (VIP) plays an important role in a variety of immunological functions. In the present report, we sorted purified thymocytes of the four major thymic subsets defined by CD4 and CD8 phenotypes. We demonstrate by reverse transcription (RT) and polymerase chain reaction (PCR) both VIP and VIP1 receptor gene expression in double positive (CD4+CD8+) and single positive (CD4+CD8-, CD4-CD8+) thymocyte subsets. Double negative thymocytes (CD4-CD8-) lack VIP and VIP1 receptor gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • CD4-CD8 Ratio
  • DNA Primers / chemistry
  • Gene Expression / genetics*
  • Male
  • Polymerase Chain Reaction
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • Receptors, Vasoactive Intestinal Peptide / biosynthesis
  • Receptors, Vasoactive Intestinal Peptide / genetics*
  • T-Lymphocyte Subsets / metabolism*
  • Thymus Gland / cytology
  • Vasoactive Intestinal Peptide / biosynthesis
  • Vasoactive Intestinal Peptide / genetics*

Substances

  • DNA Primers
  • RNA, Messenger
  • Receptors, Vasoactive Intestinal Peptide
  • Vasoactive Intestinal Peptide