Distinct roles for the SgIGSF adhesion molecule and c-kit receptor tyrosine kinase in the interaction between mast cells and the mesentery

被引:4
作者
Watabe, K
Ito, A
Koma, Y
Wakayama, T
Iseki, S
Shinomura, Y
Kitamura, Y
机构
[1] Osaka Univ, Grad Sch Med, Dept Pathol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Internal Med & Mol Sci, Suita, Osaka 5650871, Japan
[3] Kobe Univ, Grad Sch Med, Div Surg Pathol, Kobe, Hyogo 6500017, Japan
[4] Kanazawa Univ, Grad Sch Med Sci, Dept Histol & Embryol, Ishikawa 9208640, Japan
关键词
mast cells; mesentry; transmigration; SgIGSF; c-kit;
D O I
10.1016/j.bbrc.2004.09.117
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intraperitoneal injection of bone marrow-derived mast cells (BMMCs) has therapeutic efficacy against acute bacterial peritonitis. For this role, BMMCs need to settle down the mesentery from the peritoneal cavity. Interaction between BMMCs and the mesentery was examined by using mast cell deficient WBB6F(1)(F-1)- W/W-G [c-kit receptor tyrosine kinase (KIT) mutant], F-1-Sl/Sl(d) [KIT ligand stem cell factor mutant], and F-1-tg/tg [a practically microphthalmia transcription factor (MITF)-null mutant] mice. Three parameters were measured: the number of BMMCs: (1) developed in the mesentery 5 weeks after intraperitoneal injection into mast cell deficient mice, (2) adhered to mesenteric mesothelial cells, and (3) transmigrated across the mesenteric mesothelial cell monolayer when coculturing both cells for 3 and 18 h, respectively. After intraperitoneal injection, F-1-wild type (+/+) BMMCs developed in the mesentery of F-1-W/W-u mice but not in that of F-1-Sl/Sl(d) mice, while F-1-tg/tg BMMCs did not develop, even in the mesentery of WBB6F(1)-W/W-u mice. In the coculture, WB-W/W BMMCs normally adhered to but poorly transmigrated across F-1-+/+ mesothelial cells, and in accordance, F-1-+/+ BMMCs normally adhered to but poorly transmigrated across F-1-Sl/Sl(d) mesothelial cells. F(1-)tg/tg BMMCs showed poor adhesion and transmigration, but both parameters were partially but significantly improved by ectopic expression of spermatogenic immunoglobulin superfamily (SgIGSF), a mast-cell adhesion molecule critically regulated by MITF. Since F-1-tg/tg BMMCs expressed reduced levels of KIT, these results suggested that SgIGSF and KIT independently played a significant role in the transmigration. Among three parameters, development of mast cells in the mesentery well correlated with the transmigration. This process seemed important for mast cells to settle down from the peritoneal cavity to the mesentery. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:782 / 788
页数:7
相关论文
共 25 条
  • [1] ADACHI S, 1992, BLOOD, V79, P650
  • [2] AKEDO H, 1986, CANCER RES, V46, P2416
  • [3] THE PROTO-ONCOGENE C-KIT ENCODING A TRANSMEMBRANE TYROSINE KINASE RECEPTOR MAPS TO THE MOUSE W-LOCUS
    CHABOT, B
    STEPHENSON, DA
    CHAPMAN, VM
    BESMER, P
    BERNSTEIN, A
    [J]. NATURE, 1988, 335 (6185) : 88 - 89
  • [4] Critical protective role of mast cells in a model of acute septic peritonitis
    Echtenacher, B
    Mannel, DN
    Hultner, L
    [J]. NATURE, 1996, 381 (6577) : 75 - 77
  • [5] TRANSMEMBRANE FORM OF THE KIT LIGAND GROWTH-FACTOR IS DETERMINED BY ALTERNATIVE SPLICING AND IS MISSING IN THE SI(D) MUTANT
    FLANAGAN, JG
    CHAN, DC
    LEDER, P
    [J]. CELL, 1991, 64 (05) : 1025 - 1035
  • [6] THE DOMINANT-WHITE SPOTTING (W) LOCUS OF THE MOUSE ENCODES THE C-KIT PROTO-ONCOGENE
    GEISSLER, EN
    RYAN, MA
    HOUSMAN, DE
    [J]. CELL, 1988, 55 (01) : 185 - 192
  • [7] MUTATIONS AT THE MOUSE MICROPHTHALMIA LOCUS ARE ASSOCIATED WITH DEFECTS IN A GENE ENCODING A NOVEL BASIC-HELIX-LOOP-HELIX-ZIPPER PROTEIN
    HODGKINSON, CA
    MOORE, KJ
    NAKAYAMA, A
    STEINGRIMSSON, E
    COPELAND, NG
    JENKINS, NA
    ARNHEITER, H
    [J]. CELL, 1993, 74 (02) : 395 - 404
  • [8] THE HEMATOPOIETIC GROWTH FACTOR-KL IS ENCODED BY THE SI-LOCUS AND IS THE LIGAND OF THE C-KIT RECEPTOR, THE GENE-PRODUCT OF THE W-LOCUS
    HUANG, E
    NOCKA, K
    BEIER, DR
    CHU, TY
    BUCK, J
    LAHM, HW
    WELLNER, D
    LEDER, P
    BESMER, P
    [J]. CELL, 1990, 63 (01) : 225 - 233
  • [9] HUGHES MJ, 1993, J BIOL CHEM, V268, P20687
  • [10] Contribution of the SgIGSF adhesion molecule to survival of cultured mast cells in vivo
    Ito, A
    Koma, Y
    Watabe, K
    Jippo, T
    Wakayama, T
    Iseki, S
    Kitamura, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (01) : 200 - 206