Khachigian L M, Chesterman C N
University New South Wales, Department of Haematology, Prince of Wales Hospital, Randwick, Australia.
J Biol Chem. 1992 Apr 15;267(11):7478-82.
Alternative splicing results in two distinct forms of the platelet-derived growth factor (PDGF) A-chain that differ by a hydrophilic carboxyl terminus consisting of 18 amino acids (A194-211). The functional significance of this region is unclear. Previous results indicate that a radioiodinated tyrosinated synthetic peptide corresponding to A194-211 binds specifically, saturably, and with low affinity to a large population of sites on Balb/c 3T3 and several other cell lines (Khachigian, L. M., Owensby, D. A., and Chesterman, C. N. (1992) J. Biol. Chem. 267, 1660-1666). In this paper, we report that (Y)A194-211 and A194-211 can modulate the cellular proliferative response to normal human serum and several individual polypeptide growth factors as a consequence. When these peptides were coincubated separately with whole serum, PDGF, epidermal growth factor, or fibroblast growth factor, DNA synthesis was inhibited in a dose-dependent fashion and maximally by 200 microM peptide. In addition, both peptides could attenuate the stimulation of cell division by serum and PDGF. Peptides with similar charge or length failed to modify the level of proliferation. These observations were not due to cytotoxicity. Synthetic peptides such as (Y)A194-211 and A194-211 that influence cellular proliferation may be useful in modulating the cellular response to selected growth factors.
可变剪接产生了血小板衍生生长因子(PDGF)A链的两种不同形式,它们的区别在于由18个氨基酸(A194 - 211)组成的亲水性羧基末端。该区域的功能意义尚不清楚。先前的结果表明,对应于A194 - 211的放射性碘化酪氨酸化合成肽能特异性、饱和性且低亲和力地结合到Balb/c 3T3和其他几种细胞系的大量位点上(卡奇吉安,L.M.,欧文斯比,D.A.,和切斯特曼,C.N.(1992年)《生物化学杂志》267卷,1660 - 1666页)。在本文中,我们报告(Y)A194 - 211和A194 - 211能够调节细胞对正常人血清和几种单个多肽生长因子的增殖反应。当这些肽分别与全血清、PDGF、表皮生长因子或成纤维细胞生长因子共同孵育时,DNA合成以剂量依赖方式受到抑制,最大抑制程度为200 microM肽。此外,这两种肽都能减弱血清和PDGF对细胞分裂的刺激。电荷或长度相似的肽未能改变增殖水平。这些观察结果并非由于细胞毒性。像(Y)A194 - 211和A194 - 211这样影响细胞增殖的合成肽可能有助于调节细胞对特定生长因子的反应。