Boyan B D, Schwartz Z, Bonewald L F, Swain L D
Department of Orthopedics, University of Texas Health Science Center, San Antonio 78284.
J Biol Chem. 1989 Jul 15;264(20):11879-86.
Previous studies have shown 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3)-responsive alkaline phosphatase in cultured growth zone cartilage chondrocytes is localized in extracellular matrix vesicles (MV). Since osteoblast-like cells also have 1,25-(OH)2D3-responsive alkaline phosphatase, this study determined whether the 1,25-(OH)2D3-responsive enzyme activity is localized to MV produced by these cells as well. Osteoblast-like cells from rat (ROS 17/2.8), mouse (MC 3T3), human (MG 63), and rat growth zone cartilage were cultured in Dulbecco's modified Eagle's medium containing 10(-7)-10(-12) M 1,25-(OH)2D3. Alkaline phosphatase total activity and specific activity were measured in the cell layer, MV, and plasma membrane (PM) fractions. MV and PM purity were verified by electron microscopy and MV alkaline phosphatase specific activity compared to PM (MV versus PM: ROS 17/2.8 6 x; MG 63, 5.5 x; MC 3T3, 33 x; GC, 2 x). There was a dose-dependent stimulation of MV alkaline phosphatase (5- to 15-fold increase at 10(-7)-10(-9) M) in all cell types in response to the 1,25-(OH)2D3. The PM enzyme was stimulated in a parallel fashion in the osteoblast cultures. No effect of 1,25-(OH)2D3 was observed in growth cartilage PM. Although MV accounted for less than 20% of the total activity they contributed 50% of the increase in alkaline phosphatase activity in the cell layer in response to 1,25-(OH)2D3 and MV specific activity was enriched 10 times over that of the cell layer. These are common features of MV produced by cells which calcify their matrix and suggest that hormonal regulation of MV enzymes may be important in primary calcification.
以往研究表明,培养的生长区软骨细胞中1,25 - 二羟基维生素D3(1,25-(OH)2D3)反应性碱性磷酸酶定位于细胞外基质小泡(MV)中。由于成骨样细胞也有1,25-(OH)2D3反应性碱性磷酸酶,本研究确定这种1,25-(OH)2D3反应性酶活性是否也定位于这些细胞产生的MV中。将来自大鼠(ROS 17/2.8)、小鼠(MC 3T3)、人(MG 63)的成骨样细胞以及大鼠生长区软骨细胞培养于含10(-7)-10(-12) M 1,25-(OH)2D3的杜尔贝科改良伊格尔培养基中。测定细胞层、MV和质膜(PM)组分中的碱性磷酸酶总活性和比活性。通过电子显微镜验证MV和PM的纯度,并将MV碱性磷酸酶比活性与PM进行比较(MV与PM之比:ROS 17/2.8为6倍;MG 63为5.5倍;MC 3T3为33倍;生长区软骨细胞为2倍)。在所有细胞类型中,1,25-(OH)2D3均可引起MV碱性磷酸酶的剂量依赖性刺激(在10(-7)-10(-9) M时增加5至15倍)。成骨细胞培养物中的PM酶也以类似方式受到刺激。在生长软骨的PM中未观察到1,25-(OH)2D3的作用。尽管MV占总活性的比例不到20%,但它们在细胞层中对1,25-(OH)2D3反应性碱性磷酸酶活性增加的贡献达50%,且MV比活性比细胞层高10倍。这些是基质钙化细胞产生的MV的共同特征,表明MV酶的激素调节在初级钙化中可能很重要。