Dike L E, Farmer S R
Department of Biochemistry, Boston University School of Medicine, MA 02118.
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6792-6. doi: 10.1073/pnas.85.18.6792.
A methylcellulose suspension system that prevents cell-surface contact with the substrate was used to study the role of cell adhesion in the regulation of proliferation. The nonadhesive conditions established by suspension culture cause BALB/c 3T3 (A31) cells to enter a G0 state of growth arrest within 48 hr as defined by an inhibition of DNA synthesis and a suppression of c-myc and histone mRNA expression. The adhesion of these suspension-arrested cells rapidly induces c-fos, c-myc, and actin gene expression. This stimulation did not depend on the presence of serum since the adhesion of suspension-arrested cells, in the absence of serum, also induced the expression of c-fos and c-myc mRNAs. In addition, adhesion onto fibronectin increased the number of cells able to respond to epidermal growth factor and insulin and progress into S phase. These results indicate that adhesion of suspension-arrested cells activates the G0/G1 transition independent of growth factors.
一种可防止细胞表面与底物接触的甲基纤维素悬浮系统被用于研究细胞黏附在增殖调节中的作用。悬浮培养建立的非黏附条件使BALB/c 3T3(A31)细胞在48小时内进入生长停滞的G0状态,这是由DNA合成的抑制以及c-myc和组蛋白mRNA表达的抑制所定义的。这些悬浮停滞细胞的黏附迅速诱导c-fos、c-myc和肌动蛋白基因的表达。这种刺激不依赖于血清的存在,因为在无血清情况下悬浮停滞细胞的黏附也能诱导c-fos和c-myc mRNA的表达。此外,黏附到纤连蛋白上增加了能够对表皮生长因子和胰岛素作出反应并进入S期的细胞数量。这些结果表明,悬浮停滞细胞的黏附激活了G0/G1期转换,且不依赖于生长因子。