Oda K
Department of Biochemistry, Fukuoka University School of Medicine, Japan.
J Biol Chem. 1992 Aug 25;267(24):17465-71.
The effects of calcium depletion on the proteolytic cleavage and secretion of plasma protein precursors were investigated in primary cultured rat hepatocytes and HepG2 cells. When the cells were incubated with A23187, the calcium-specific ionophore, in a medium lacking CaCl2, precursors of serum albumin and the third and fourth components of complement, C3 and C4, respectively, were found to be released into the medium. The addition of ionomycin or EGTA to the medium inhibited the processing of pro-C3 as well. Blocking the secretory pathway either at the mixed endoplasmic reticulum/Golgi in the presence of brefeldin A or at the endoplasmic reticulum/tubular-vesicular structure at a reduced temperature caused accumulation of pro-C3 within hepatocytes or HepG2 cells, indicating that the cleavage of the precursor occurs at a later stage of the secretory pathway. Once the blockade was released by incubating the cells either in the brefeldin A-free medium or at 37 degrees C, the secretion of plasma proteins resumed, irrespective of the presence of A23187. However, the processing of pro-C3 was almost completely inhibited in the presence of A23187, with only the precursor being released into the medium, implying that a decline in Ca2+ levels within the cell modulates the activity of a Golgi endoprotease responsible for the cleavage of pro-C3. When incubated with isolated Golgi membranes, pro-C3 secreted from Ca(2+)-depleted cells was cleaved in vitro into their subunits in the presence of Ca2+ but not in its absence, pointing to the involvement of a Ca(2+)-dependent Golgi endoprotease in the processing of pro-C3. These results collectively suggest that calcium depletion blocks the proteolytic cleavages of plasma protein precursors presumably by exhausting a Ca2+ pool available to the Ca(2+)-dependent processing enzyme(s) located at the Golgi and/or trans-Golgi network.
在原代培养的大鼠肝细胞和HepG2细胞中研究了钙耗竭对血浆蛋白前体蛋白水解切割和分泌的影响。当细胞在缺乏CaCl2的培养基中与钙特异性离子载体A23187一起孵育时,发现血清白蛋白以及补体第三和第四成分C3和C4的前体分别释放到培养基中。向培养基中添加离子霉素或EGTA也抑制了前C3的加工。在布雷菲德菌素A存在的情况下在内质网/高尔基体混合部位或在低温下在内质网/管状小泡结构处阻断分泌途径,导致前C3在肝细胞或HepG2细胞内积累,表明前体的切割发生在分泌途径的后期。一旦通过在无布雷菲德菌素A的培养基中孵育细胞或在37℃下孵育来解除阻断,血浆蛋白的分泌就会恢复,而不管A23187是否存在。然而,在A23187存在的情况下,前C3的加工几乎完全受到抑制,只有前体释放到培养基中,这意味着细胞内Ca2+水平的下降调节了负责前C3切割 的高尔基体内切蛋白酶的活性。当与分离的高尔基体膜一起孵育时,从Ca(2+)耗尽的细胞分泌的前C3在有Ca2+存在的情况下在体外被切割成其亚基,而在没有Ca2+的情况下则不会,这表明一种Ca(2+)依赖性高尔基体内切蛋白酶参与了前C3的加工。这些结果共同表明,钙耗竭可能通过耗尽位于高尔基体和/或反式高尔基体网络的Ca(2+)依赖性加工酶可用的Ca2+池来阻断血浆蛋白前体的蛋白水解切割。