Mesenchymal cells stimulate human intestinal intraepithelial lymphocytes

• Published in: Gastroenterology (New York, N.Y. 1943) Vol. 113; no. 1; p. 144
• Main Authors: Roberts, A I, Nadler, S C, Ebert, E C
• Format: Journal Article
• Language: English
• Published: United States 01.07.1997
• Subjects: CD8-Positive T-Lymphocytes - cytology; Cell Division; Coculture Techniques; Enzyme-Linked Immunosorbent Assay; Fibroblasts - cytology; Histocompatibility Antigens Class I - physiology; Humans; Immunity, Mucosal; Integrin alpha4beta1; Integrins - physiology; Interleukin-2 - biosynthesis; Intestinal Mucosa - cytology; Jejunum - cytology; Muscle, Smooth - cytology; Receptors, Lymphocyte Homing - physiology; Receptors, Very Late Antigen - physiology
• ISSN: 0016-5085
• DOI: 10.1016/S0016-5085(97)70089-1

Intraepithelial lymphocytes (IELs) from human intestinal mucosa proliferate minimally to T-cell stimuli. Optimal growth may depend on factors that are missing in vitro, such as accessory cells. The aim of this study was to determine whether mesenchymal cells costimulate IELs. IELs were isolated from human jejunum and cultured with fibroblasts or smooth muscle cells (mesenchymal cell models for mucosal myofibroblasts) and various T-cell stimuli. Proliferation was determined by [3H]thymidine incorporation, and interleukin 2 (IL-2) production was measured by enzyme-linked immunosorbent assay. Surface molecules were detected by immunofluorescence and flow cytometry. The proliferative responses of IELs to mitogen (phytohemagglutinin), superantigen (staphylococcal enterotoxin B), or anti-CD3 antibody were increased greatly by coculture with mesenchymal cells, while only slightly by peripheral-blood monocytes, the classical antigen-presenting cells. IL-2 production and receptor expression also increased. Mesenchymal cell costimulation of IEL growth required direct contact between the two cell types and was partly dependent on the integrin alpha4beta1 (very late activation 4[VLA-4]) and major histocompatibility complex (MHC) class I, as their respective antibodies blocked the effect. The surface molecules B7 (CD80), CD2, and MHC class II were not involved. Optimal IEL growth depends on their contact with mesenchymal cells, an interaction that is mediated by VLA-4 and MHC class I. In mucosal immunity, basement membrane myofibroblasts likely serve this role.