Differential expression of neurotensin and specific receptors, NTSR1 and NTSR2, in normal and malignant human B lymphocytes

J Immunol. 2012 Dec 1;189(11):5293-303. doi: 10.4049/jimmunol.1102937. Epub 2012 Oct 29.

Abstract

Neurotensin, a neuropeptide growth factor, and its two specific neurotensin receptors, NTSR1 and NTSR2, were shown to be expressed by human B cell lines. Another NTSR, sortilin, which is common to neurotensin and neurotrophins, was also detected as we have previously described. Neurotensin was functional in B cell lines; it induced their proliferation and inhibited apoptosis induced by serum deprivation or Fas activation. Quantitative study of gene expression in two malignant B cell diseases showed that NTSR2 was overexpressed, NTSR1 decreased, and neurotensin was unexpressed in B cell leukemia patient's cells, as compared with healthy B cells. However, these expressions did not significantly change in large diffuse B cell lymphoma lymph nodes compared with benign ones. This study points out that neurotensin and its two specific receptors are expressed in human B lymphocytes. Such expressions were not described, and their relationship in B cell diseases, especially in chronic B cell leukemia, needs to be considered further in regard to these findings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • B-Lymphocytes / metabolism*
  • B-Lymphocytes / pathology
  • Carcinoma / genetics
  • Carcinoma / metabolism
  • Carcinoma / pathology
  • Case-Control Studies
  • Cell Line, Tumor
  • Cell Proliferation
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Lymphoma, Large B-Cell, Diffuse / genetics*
  • Lymphoma, Large B-Cell, Diffuse / metabolism
  • Lymphoma, Large B-Cell, Diffuse / pathology
  • Neurotensin / genetics*
  • Neurotensin / metabolism
  • Organ Specificity
  • Primary Cell Culture
  • Receptors, Neurotensin / genetics*
  • Receptors, Neurotensin / metabolism
  • Signal Transduction
  • fas Receptor / genetics
  • fas Receptor / metabolism

Substances

  • FAS protein, human
  • NTSR2 protein, human
  • Receptors, Neurotensin
  • fas Receptor
  • neurotensin type 1 receptor
  • Neurotensin