Tsujimura T, Koshimizu U, Katoh H, Isozaki K, Kanakura Y, Tono T, Adachi S, Kasugai T, Tei H, Nishimune Y
Department of Pathology, Medical School, Osaka University, Japan.
Blood. 1993 May 15;81(10):2530-8.
The W locus of mice encodes the c-kit receptor tyrosine kinase. Heterozygous WJic/+ and Wn/+ mice and homozygous Wf/Wf mice were similar in appearance; all of them have large depigmented areas lacking any well-defined pattern. The WJic, Wn, and Wf mutant alleles were characterized and their molecular nature was correlated with the mast cell differentiation in the skin and the biologic features of cultured mast cell (CMC). All WJic, Wn, and Wf were point mutations at the tyrosine kinase domain, and c-kit mRNA was normally transcribed from all of them. The mature 145-Kd form of the c-kit protein was produced from the WJic and Wf alleles, but not from the Wn allele. c-kit proteins produced by the WJic or Wf allele were expressed on the surface of CMCs, but those of the Wn allele were not. When double heterozygous mice were produced between W and WJic and between W and Wn, both W/WJic and W/Wn mice lacked skin mast cells. W/WJic CMCs and W/Wn CMCs did not survive in the coculture with fibroblasts. W/WJic CMCs normally attached to fibroblasts, but W/Wn CMCs did not. The defect of W/Wn CMCs in the attachment was attributed to the deficient extracellular expression of the c-kit protein. The number of skin mast cells was compared among WJic/+, Wn/+, Wf/+, and Wf/Wf mice. Mast cells decreased in WJic/+ and Wf/Wf mice, but not in Wn/+ and Wf/+ mice. Although the Wn was a point mutation at the kinase domain, the biologic effect of the Wn was comparable with that of the W mutant allele, which produces truncated c-kit protein without the transmembrane domain. The weak phenotype of Wn/+ mice may be explained by the deficient extracellular expression of c-kit proteins produced by the Wn allele. When WJic/WJic, Wn/Wn, and Wf/Wf CMCs were stimulated by the recombinant c-kit ligand, autophosphorylation activity was observed only in Wf/Wf CMCs. This result was consistent with the weak biologic effect of the Wf mutant allele.
小鼠的W基因座编码c-kit受体酪氨酸激酶。杂合子WJic/+和Wn/+小鼠以及纯合子Wf/Wf小鼠外观相似;它们都有大片色素脱失区域,且无明确的图案。对WJic、Wn和Wf突变等位基因进行了表征,并将它们的分子性质与皮肤中的肥大细胞分化以及培养的肥大细胞(CMC)的生物学特性相关联。所有WJic、Wn和Wf均为酪氨酸激酶结构域的点突变,并且c-kit mRNA从它们所有中正常转录。c-kit蛋白的成熟145-Kd形式由WJic和Wf等位基因产生,但不由Wn等位基因产生。由WJic或Wf等位基因产生的c-kit蛋白在CMC表面表达,但Wn等位基因的蛋白则不表达。当在W与WJic之间以及W与Wn之间产生双杂合子小鼠时,W/WJic和W/Wn小鼠均缺乏皮肤肥大细胞。W/WJic CMC和W/Wn CMC在与成纤维细胞共培养时无法存活。W/WJic CMC通常附着于成纤维细胞,但W/Wn CMC则不然。W/Wn CMC附着缺陷归因于c-kit蛋白细胞外表达不足。比较了WJic/+、Wn/+、Wf/+和Wf/Wf小鼠的皮肤肥大细胞数量。WJic/+和Wf/Wf小鼠中的肥大细胞减少,但Wn/+和Wf/+小鼠中则未减少。尽管Wn是激酶结构域的点突变,但其生物学效应与产生无跨膜结构域的截短c-kit蛋白的W突变等位基因相当。Wn/+小鼠的弱表型可能由Wn等位基因产生的c-kit蛋白细胞外表达不足来解释。当用重组c-kit配体刺激WJic/WJic、Wn/Wn和Wf/Wf CMC时,仅在Wf/Wf CMC中观察到自磷酸化活性。该结果与Wf突变等位基因的弱生物学效应一致。