Ibrahim M, Upreti R K, Kidwai A M
Biomembrane Division, Industrial Toxicology Research Centre, Lucknow, India.
Mol Cell Biochem. 1994 Feb 9;131(1):49-59. doi: 10.1007/BF01075724.
Micromolar and millimolar Ca(2+)-requiring neutral protease (calpain I and calpain II) along with their endogenous inhibitor calpastatin were isolated and partially purified from the same preparation of rat intestinal epithelial cells. Calpain I and II were partially purified by 1300 and 900-fold with 57 and 53 per cent yield, respectively. The optimum assay conditions revealed pH 7.5, 20 min incubation at 25 degrees C and 0.24% casein substrate for both calpains. The optimum calcium concentration obtained for calpain I and II were 25 microM and 4 mM, respectively. Distribution of rat intestinal epithelial cells calpain I and II along with calpastatin during cell differentiation stages in weanling to senescence age were studied. Calpain I in weanling rats was in an increasing order from villus to crypt regions. Adult rats indicated well expressed consistent calpain I throughout the differentiation stages. Whereas, significant lowering towards crypt region cells were evident in old rats. Calpain II in weanling and adult rats was found to be consistent throughout the differentiation stages. Old animals revealed an increasing trend from villus to crypt region with insignificant activity present in upper villus cells. Concomitantly, different concentrations of calpastatin were observed throughout the differentiation stages in all the age groups. Moreover, the levels of calpains exceeded that of calpastatin in most of the epithelial cell populations during developmental stages. In addition to casein, intestinal epithelial cell membranes were found to be equally good substrates for calpains. Proteolytic susceptibility of weanling, adult and old rat membrane proteins varied significantly all along the ageing process in rats. Simultaneous age-dependent calpastatin response were also evident. Taken together the results obtained provided strong evidence that calpain plays significant role in rat intestinal cell differentiation and ageing process with calpastatin as its specific regulatory protein.
从大鼠肠上皮细胞的同一制备物中分离并部分纯化了需要微摩尔和毫摩尔钙的中性蛋白酶(钙蛋白酶I和钙蛋白酶II)及其内源性抑制剂钙蛋白酶抑制蛋白。钙蛋白酶I和II分别以57%和53%的产率部分纯化了1300倍和900倍。最佳测定条件显示,两种钙蛋白酶的pH值均为7.5,在25℃孵育20分钟,酪蛋白底物浓度为0.24%。钙蛋白酶I和II的最佳钙浓度分别为25μM和4mM。研究了大鼠肠上皮细胞钙蛋白酶I和II以及钙蛋白酶抑制蛋白在断奶至衰老阶段细胞分化过程中的分布。断奶大鼠的钙蛋白酶I从绒毛区到隐窝区呈递增顺序。成年大鼠在整个分化阶段钙蛋白酶I表达一致。然而,老年大鼠隐窝区细胞中的钙蛋白酶I明显降低。断奶和成年大鼠的钙蛋白酶II在整个分化阶段是一致的。老年动物从绒毛区到隐窝区呈增加趋势,上绒毛细胞中的活性不明显。同时,在所有年龄组的整个分化阶段都观察到了不同浓度的钙蛋白酶抑制蛋白。此外,在发育阶段的大多数上皮细胞群体中,钙蛋白酶的水平超过了钙蛋白酶抑制蛋白的水平。除了酪蛋白外,还发现肠上皮细胞膜是钙蛋白酶的良好底物。断奶、成年和老年大鼠膜蛋白的蛋白水解敏感性在大鼠衰老过程中均有显著差异。同时,年龄依赖性的钙蛋白酶抑制蛋白反应也很明显。综合所得结果提供了有力证据,表明钙蛋白酶在大鼠肠细胞分化和衰老过程中起重要作用,钙蛋白酶抑制蛋白是其特异性调节蛋白。