Sizeland A M, Burgess A W
Melbourne Tumour Biology Branch, Ludwig Institute for Cancer Research, Victoria, Australia.
Mol Cell Biol. 1991 Aug;11(8):4005-14. doi: 10.1128/mcb.11.8.4005-4014.1991.
The role of autocrine growth factors in tumor cell growth has been difficult to prove. Our results indicate that more than one autocrine factor is required for the autonomous growth of the LIM 1215 colonic carcinoma cell line. Furthermore, the morphologic changes induced by epidermal growth factor (EGF) are also density dependent and appear to require a synergistic autocrine factor. The serum-free proliferation of the colonic carcinoma cell line LIM 1215 depends on cell density and the presence of EGF (A. Sizeland, S. Bol, and A.W. Burgess, Growth Factors 4:129-143, 1991). At cell densities below 10(4)/cm2, conditioned medium (from cells at a density of 10(5)/cm2) was required for the cells to elicit a mitogenic response to exogenous EGF. At higher cell densities (10(5)/cm2), the cells were independent of both exogenous EGF and conditioned medium. In addition, the EGF receptor was found to be phosphorylated on tyrosine in LIM 1215 cells proliferating at high density, suggesting that the autocrine production of transforming growth factor alpha (TGF alpha) and subsequent ligation to the EGF receptor was occurring. The proliferation of cells at high density was partly inhibited by TGF alpha antibodies but was almost completely inhibited by an antisense oligonucleotide to TGF alpha. The antisense inhibition could be overcome by the addition of EGF, indicating that the effect of the antisense TGF alpha oligonucleotide was on the production of autocrine TGF alpha. LIM 1215 cells were also observed to undergo morphologic changes (spreading and actin cable organization) in response to EGF. These changes were density dependent, but they occurred with a cell density dependence different from that of the proliferative response. These results suggest two possibilities: that the morphologic changes and proliferative responses have different sensitivities to the autocrine factors or that the actions of the autocrine factors are mediated through different signal transduction pathways.
自分泌生长因子在肿瘤细胞生长中的作用一直难以证实。我们的结果表明,LIM 1215结肠癌细胞系的自主生长需要不止一种自分泌因子。此外,表皮生长因子(EGF)诱导的形态学变化也是密度依赖性的,并且似乎需要一种协同自分泌因子。结肠癌细胞系LIM 1215在无血清条件下的增殖取决于细胞密度和EGF的存在(A. Sizeland、S. Bol和A.W. Burgess,《生长因子》4:129 - 143,1991)。在细胞密度低于10⁴/cm²时,细胞对外源性EGF产生促有丝分裂反应需要条件培养基(来自密度为10⁵/cm²的细胞)。在较高细胞密度(10⁵/cm²)时,细胞对外源性EGF和条件培养基均不依赖。此外,发现在高密度增殖的LIM 1215细胞中,EGF受体的酪氨酸发生了磷酸化,这表明正在发生转化生长因子α(TGFα)的自分泌产生以及随后与EGF受体的结合。高密度细胞的增殖部分受到TGFα抗体的抑制,但几乎完全受到针对TGFα的反义寡核苷酸的抑制。添加EGF可以克服反义抑制,这表明反义TGFα寡核苷酸的作用是针对自分泌TGFα的产生。还观察到LIM 1215细胞对EGF有形态学变化(铺展和肌动蛋白丝束组织)。这些变化是密度依赖性的,但它们发生时的细胞密度依赖性与增殖反应不同。这些结果提示了两种可能性:形态学变化和增殖反应对自分泌因子具有不同的敏感性,或者自分泌因子的作用是通过不同的信号转导途径介导的。