Higashiyama S, Abraham J A, Klagsbrun M
Department of Surgical Research, Children's Hospital, Boston, Mass 02115.
Horm Res. 1994;42(1-2):9-13. doi: 10.1159/000184137.
Heparin-binding epidermal growth factor-like growth factor (HB-EGF) has been previously demonstrated to be a potent mitogen for smooth muscle cells. Evidence is now presented that these cells synthesize HB-EGF as well. Cultured fetal human vascular smooth muscle cells express 2.5-kb HB-EGF mRNA. These cells also release an HB-EGF-like activity that (i) stimulates smooth muscle cell and BALB/c 3T3 cell but not endothelial cell proliferation; (ii) binds to TSK heparin affinity columns and is eluted with 0.9-1.2 M NaCl, and (iii) triggers phosphorylation of a protein with the same molecular weight as the 170-kD EGF receptor. In addition, 125I-HB-EGF can be cross-linked to the EGF receptor on fetal human vascular smooth muscle cells. These results suggest that smooth muscle cells can both synthesize and respond to HB-EGF, and that HB-EGF may therefore be involved in autocrine regulation of these cells.
肝素结合表皮生长因子样生长因子(HB-EGF)先前已被证明是平滑肌细胞的一种强效促有丝分裂原。现在有证据表明这些细胞也能合成HB-EGF。培养的人胎儿血管平滑肌细胞表达2.5 kb的HB-EGF mRNA。这些细胞还释放出一种HB-EGF样活性物质,其具有以下特性:(i)刺激平滑肌细胞和BALB/c 3T3细胞增殖,但不刺激内皮细胞增殖;(ii)与TSK肝素亲和柱结合,并用0.9 - 1.2 M NaCl洗脱,以及(iii)触发与170-kD表皮生长因子受体分子量相同的一种蛋白质的磷酸化。此外,125I-HB-EGF可与胎儿人血管平滑肌细胞上的表皮生长因子受体交联。这些结果表明平滑肌细胞既能合成HB-EGF又能对其作出反应,因此HB-EGF可能参与这些细胞的自分泌调节。