Human intestinal intraepithelial lymphocytes have potent chemotactic activity

Gastroenterology. 1995 Oct;109(4):1154-9. doi: 10.1016/0016-5085(95)90573-1.

Abstract

Background & aims: Inflammation is created by the movement of leukocytes toward soluble attractants (chemokines). The aim of this study was to identify the chemokines that attract intestinal lymphocytes.

Methods: Intraepithelial and lamina propria lymphocytes were isolated from human jejunal mucosa of healthy individuals and cultured in interleukin (IL) 2 for 3 days. Migration was assessed using the Boyden transwell assay. Increases in cytoplasmic calcium ion concentration ([Ca2+]i) were measured from changes in fluorescence in Fura-2-loaded lymphocytes on exposure to the cytokines.

Results: A large number of intraepithelial lymphocytes migrated toward IL-8 and RANTES (regulated on activation, normal T cell expressed and secreted), and a small number migrated toward IL-10. In contrast, only a few lamina propria lymphocytes migrated toward IL-8, and none responded to the other chemokines tested. The chemokines IL-8 and IL-10, but not RANTES, increased [Ca2+]i in intraepithelial lymphocytes; this calcium mobilization was not affected by ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid, indicating that calcium is released from intracellular sources. None of the factors caused calcium mobilization by lamina propria lymphocytes.

Conclusions: This study shows that intraepithelial lymphocytes have greater migratory and calcium-mobilizing activity than lamina propria lymphocytes and that these two activities do not correlate with each other.

Publication types

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

MeSH terms

  • Calcium / metabolism
  • Cells, Cultured
  • Chemokine CCL5 / physiology
  • Chemotaxis, Leukocyte / physiology*
  • Epithelial Cells
  • Humans
  • Interleukin-10 / physiology
  • Interleukin-8 / physiology
  • Intestinal Mucosa / cytology*
  • Jejunum / cytology
  • Lymphocytes / physiology*

Substances

  • Chemokine CCL5
  • Interleukin-8
  • Interleukin-10
  • Calcium