Shipley G D, Keeble W W, Hendrickson J E, Coffey R J, Pittelkow M R
Department of Cell Biology and Anatomy, School of Medicine, Oregon Health Sciences University, Portland 97201.
J Cell Physiol. 1989 Mar;138(3):511-8. doi: 10.1002/jcp.1041380310.
Keratinocytes and fibroblasts isolated from human neonatal foreskin can be plated and grown through multiple rounds of division in vitro under defined serum-free conditions. We utilized these growth conditions to examine the mitogenic potential of acidic and basic fibroblast growth factor (aFGF and bFGF) on these cells. Our results demonstrate that both aFGF and bFGF can stimulate the proliferation of keratinocytes and fibroblasts. aFGF is a more potent mitogen than bFGF for keratinocytes. In contrast, bFGF appears to be more potent than aFGF in stimulating the growth of fibroblast cultures. Heparin sulfate (10 micrograms/ml) dramatically inhibited the ability of bFGF to stimulate the proliferation of keratinocytes. In comparison, heparin slightly inhibited the stimulatory effect of aFGF and had no effect on epidermal growth factor (EGF) stimulation in keratinocyte cultures. In fibroblast cultures the addition of heparin enhanced the mitogenic effect of aFGF, had a minimal stimulatory effect on the mitogenic activity of bFGF, and had no effect on EGF-stimulated growth. Our results demonstrate that the proliferation in vitro of two normal cell types found in the skin can be influenced by aFGF and bFGF and demonstrate cell-type specific differences in the responsiveness of fibroblasts and keratinocytes to these growth factors and heparin.
从人新生儿包皮分离出的角质形成细胞和成纤维细胞,可在特定无血清条件下进行体外接种,并经过多轮分裂生长。我们利用这些生长条件来检测酸性和碱性成纤维细胞生长因子(aFGF和bFGF)对这些细胞的促有丝分裂潜力。我们的结果表明,aFGF和bFGF均可刺激角质形成细胞和成纤维细胞的增殖。对于角质形成细胞而言,aFGF是比bFGF更强效的有丝分裂原。相比之下,bFGF在刺激成纤维细胞培养物生长方面似乎比aFGF更有效。硫酸乙酰肝素(10微克/毫升)显著抑制bFGF刺激角质形成细胞增殖的能力。相比之下,肝素轻微抑制aFGF的刺激作用,并且对角质形成细胞培养物中表皮生长因子(EGF)的刺激作用没有影响。在成纤维细胞培养物中,添加肝素增强了aFGF的促有丝分裂作用,对bFGF的促有丝分裂活性具有最小的刺激作用,并且对EGF刺激的生长没有影响。我们的结果表明,皮肤中发现的两种正常细胞类型的体外增殖可受到aFGF和bFGF的影响,并证明了成纤维细胞和角质形成细胞对这些生长因子和肝素的反应性存在细胞类型特异性差异。