Adachi S, Tsujimura T, Jippo T, Morimoto M, Isozaki K, Kasugai T, Nomura S, Kitamura Y
Department of Pathology, Osaka University Medical School, Suita, Japan.
Exp Hematol. 1995 Jan;23(1):58-65.
Cultured mast cells (CMC) derived from the bone marrow of mice express the receptor encoded by the W (c-kit) locus (W receptor), and the WCB6F1(+/+)-3T3 fibroblasts express the ligand encoded by the Sl locus (stem cell factor [SCF]). CMC attach to the fibroblasts through the W receptors and cell-bound SCF. We investigated the effect of phorbol 12-myristate 13-acetate (PMA) and recombinant murine SCF (rmSCF) on the attachment. PMA induced both the internalization and shedding of W receptors, whereas rmSCF induced only the internalization. Moreover, both PMA and rmSCF reduced the expression of c-kit mRNA levels in CMC. Addition of either PMA or rmSCF to the coculture of CMC and fibroblasts resulted in the inhibition of attachment. Since the magnitude of the attachment between CMC and fibroblasts may be manipulated by changing the doses of either PMA or rmSCF, the present experimental system may be useful as a model for the attachment between blood cells and stromal cells.
从小鼠骨髓中分离培养的肥大细胞(CMC)表达由W(c-kit)基因座编码的受体(W受体),而WCB6F1(+/+)-3T3成纤维细胞表达由Sl基因座编码的配体(干细胞因子[SCF])。CMC通过W受体和细胞结合的SCF附着于成纤维细胞。我们研究了佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)和重组鼠SCF(rmSCF)对这种附着的影响。PMA诱导W受体的内化和脱落,而rmSCF仅诱导内化。此外,PMA和rmSCF均降低了CMC中c-kit mRNA的表达水平。将PMA或rmSCF添加到CMC与成纤维细胞的共培养体系中均导致附着受到抑制。由于CMC与成纤维细胞之间附着的程度可通过改变PMA或rmSCF的剂量来调控,因此本实验体系可作为血细胞与基质细胞之间附着的模型。