Potts J D, Dagle J M, Walder J A, Weeks D L, Runyan R B
Department of Anatomy, University of Iowa, Iowa City 52242.
Proc Natl Acad Sci U S A. 1991 Feb 15;88(4):1516-20. doi: 10.1073/pnas.88.4.1516.
During early cardiac development, the progenitor cells of the heart valves and membranous septa undergo an epithelial-mesenchymal transformation. Previous studies have shown that this transformation depends on the activity of a transforming growth factor beta (TGF beta) molecule produced by the heart. In the present study, we have used modified antisense oligodeoxynucleotides generated to nonconserved regions of TGF beta 1, -2, -3, and -4 to examine the possible roles of these members in this transformation. A phosphoramidate-modified oligonucleotide complementary to TGF beta 3 mRNA was capable of inhibiting normal epithelial-mesenchymal transformation by 80%. Unmodified oligonucleotides to TGF beta 3, modified oligonucleotides to TGF beta 1, -2, and -4, and two modified control oligonucleotides were unable to inhibit the transformation. These data demonstrate that a specific member of the TGF beta family, TGF beta 3, is essential for the epithelial-mesenchymal cell transformation.
在心脏发育早期,心脏瓣膜和膜性间隔的祖细胞会经历上皮-间充质转化。先前的研究表明,这种转化依赖于心脏产生的一种转化生长因子β(TGFβ)分子的活性。在本研究中,我们使用针对TGFβ1、-2、-3和-4非保守区域生成的修饰反义寡脱氧核苷酸,来研究这些成员在这种转化中可能发挥的作用。与TGFβ3 mRNA互补的磷酰胺修饰寡核苷酸能够将正常上皮-间充质转化抑制80%。针对TGFβ3的未修饰寡核苷酸、针对TGFβ1、-2和-4的修饰寡核苷酸以及两种修饰对照寡核苷酸均无法抑制这种转化。这些数据表明,TGFβ家族的一个特定成员TGFβ3对于上皮-间充质细胞转化至关重要。