Bauer E A, Silverman N, Busiek D F, Kronberger A, Deuel T F
Science. 1986 Dec 5;234(4781):1240-3. doi: 10.1126/science.3022382.
Patients with Werner's syndrome, an autosomal recessive disorder, undergo an accelerated aging process that leads to premature death. Fibroblasts from such patients typically grow poorly in culture. Here it is shown that fibroblasts from a patient with Werner's syndrome have a markedly attenuated mitogenic response to platelet-derived growth factor (PDGF) and fibroblast growth factor (FGF). In contrast, they have a full mitogenic response to fetal bovine serum. Both PDGF binding and receptor numbers per cell are unaltered. The Werner's syndrome cells express high constitutive levels of collagenase in vitro. Although PDGF enhances collagenase expression through increased levels of hybridizable collagenase messenger RNA in normal skin fibroblasts, no induction of collagenase occurs in the Werner's syndrome fibroblasts. Moreover, the failure to respond to this agonist effect of PDGF is not restored by fetal bovine serum. The data suggest that failure of one or more PDGF-mediated pathways in Werner's syndrome cells may contribute to the phenotypic expression of the disorder.
患有常染色体隐性疾病沃纳综合征的患者会经历加速衰老过程,最终导致过早死亡。这类患者的成纤维细胞在培养中通常生长不良。本文表明,一名沃纳综合征患者的成纤维细胞对血小板衍生生长因子(PDGF)和成纤维细胞生长因子(FGF)的促有丝分裂反应明显减弱。相比之下,它们对胎牛血清有完全的促有丝分裂反应。每个细胞的PDGF结合和受体数量均未改变。沃纳综合征细胞在体外表达高水平的组成型胶原酶。虽然PDGF通过增加正常皮肤成纤维细胞中可杂交的胶原酶信使核糖核酸水平来增强胶原酶表达,但在沃纳综合征成纤维细胞中未发生胶原酶的诱导。此外,胎牛血清不能恢复对PDGF这种激动剂效应的无反应状态。这些数据表明,沃纳综合征细胞中一个或多个PDGF介导的途径功能障碍可能导致该疾病的表型表达。