Murray S S, Grisanti M S, Bentley G V, Kahn A J, Urist M R, Murray E J
Geriatric Research, Education and Clinical Center, Department of Veterans Affairs Medical Center, Sepulveda, California 91343, USA.
Exp Cell Res. 1997 Jun 15;233(2):297-309. doi: 10.1006/excr.1997.3550.
The calpain-calpastatin system, which consists of calpains I and II (two ubiquitously distributed calcium-activated papain-like cysteine proteases), as well as calpastatin (the endogenous calpain inhibitor), plays an important role in cell proliferation and differentiation in many tissues. However, its contribution to the regulation of osteoprogenitor or pluripotent stem cell proliferation and differentiation into osteoblasts remains poorly defined. In these studies, rat pluripotent mesodermal cells (ROB-C26) and mouse MC3T3-E1 preosteoblasts were induced to differentiate into osteoblasts by long-term culture or in response to bone morphogenetic protein (BMP). The occurrence and distribution of calpain-calpastatin system proteins were determined by immunofluorescent microscopy, measurement of calcium-dependent proteolytic activity, and Western blotting. Treatment of intact MC3T3-E1 cells with an irreversible, membrane-permeable cysteine protease inhibitor attenuated proliferation and alkaline phosphatase upregulation under differentiation-enhancing conditions. Calpain II activity increased during differentiation of MC3T3-E1 cells in postconfluent culture. When ROB-C26 cells were maintained in long-term culture, neutral protease, calpain I, and calpain II activities increased 2- to 3-fold in the absence of BMP. In the presence of partially purified native BMP, neutral protease and calpain I activities also increased similarly, but calpain II activity increased by 10-fold in 3 days. The maximal increase in alkaline phosphatase occurred 4 to 11 days after the calpain II activity had peaked. Induction of differentiation in long-term MC3T3-E1 cultures was associated with higher calpain II and 70- and 110-kDa calpastatin protein levels and lower 17-kDa calpastatin degradation product levels. In conclusion, cysteine protease activity is essential for preosteoblastic proliferation and differentiation. The calpain-calpastatin system is regulated during osteoprogenitor proliferation and differentiation, as it is in other cells, and bone morphogenetic protein is a specific regulator of calpain II.
钙蛋白酶 - 钙蛋白酶抑制蛋白系统由钙蛋白酶I和II(两种广泛分布的钙激活木瓜蛋白酶样半胱氨酸蛋白酶)以及钙蛋白酶抑制蛋白(内源性钙蛋白酶抑制剂)组成,在许多组织的细胞增殖和分化中起重要作用。然而,其对骨祖细胞或多能干细胞增殖以及分化为成骨细胞的调节作用仍不清楚。在这些研究中,大鼠多能中胚层细胞(ROB - C26)和小鼠MC3T3 - E1前成骨细胞通过长期培养或响应骨形态发生蛋白(BMP)被诱导分化为成骨细胞。通过免疫荧光显微镜、钙依赖性蛋白水解活性测定和蛋白质印迹法确定钙蛋白酶 - 钙蛋白酶抑制蛋白系统蛋白的出现和分布。在增强分化的条件下,用不可逆的、可透过膜的半胱氨酸蛋白酶抑制剂处理完整的MC3T3 - E1细胞可减弱增殖并抑制碱性磷酸酶上调。在汇合后培养的MC3T3 - E1细胞分化过程中,钙蛋白酶II活性增加。当ROB - C26细胞进行长期培养时,在无BMP的情况下,中性蛋白酶、钙蛋白酶I和钙蛋白酶II活性增加2至3倍。在存在部分纯化的天然BMP的情况下,中性蛋白酶和钙蛋白酶I活性也有类似增加,但钙蛋白酶II活性在3天内增加了10倍。碱性磷酸酶的最大增加发生在钙蛋白酶II活性达到峰值后的4至11天。长期MC3T3 - E1培养物中的分化诱导与较高的钙蛋白酶II以及70 kDa和110 kDa钙蛋白酶抑制蛋白水平和较低的17 kDa钙蛋白酶抑制蛋白降解产物水平相关。总之,半胱氨酸蛋白酶活性对于前成骨细胞的增殖和分化至关重要。钙蛋白酶 - 钙蛋白酶抑制蛋白系统在骨祖细胞增殖和分化过程中受到调节,就像在其他细胞中一样,并且骨形态发生蛋白是钙蛋白酶II的特异性调节剂。