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1,25 - 二羟维生素D3和24,25 - 二羟维生素D3对生长区和静止区软骨细胞膜碱性磷酸酶及磷脂酶A2比活性的直接影响。

Direct effects of 1,25-dihydroxyvitamin D3 and 24,25-dihydroxyvitamin D3 on growth zone and resting zone chondrocyte membrane alkaline phosphatase and phospholipase-A2 specific activities.

作者信息

Schwartz Z, Schlader D L, Swain L D, Boyan B D

机构信息

Department of Orthopedics, University of Texas Health Science Center, San Antonio 78284.

出版信息

Endocrinology. 1988 Dec;123(6):2878-84. doi: 10.1210/endo-123-6-2878.

Abstract

1,25-Dihydroxyvitamin D3 [1,25-(OH)2D3] and 24,25-(OH)2D3 differentially affect the specific activity of alkaline phosphatase (ALPase) and phospholipase-A2 (PLA2) of plasma membranes and extracellular matrix vesicles produced by costochondral reserve zone and growth zone cartilage chondrocytes in culture. In the present study, growth zone and cartilage and reserve zone matrix vesicles and plasma membranes were isolated from confluent chondrocyte cultures and incubated with hormone for 3 and 24 h in vitro. Addition of 1,25-(OH)2D3 to GC matrix vesicles and plasma membranes resulted in dose-dependent increases in ALPase and PLA2 specific activities in both membrane fractions. Addition of 24,25-(OH)2D3 to RC membrane fractions stimulated matrix vesicle ALPase at 10(-7) and 10(-8) M and plasma membrane ALPase at 10(-8) M only. However, 24,25-(OH)2D3 inhibited matrix vesicle and plasma membrane PLA2 activity. The effects of the vitamin D metabolites were noticed after both 3 and 24 h. Neither hormone metabolite had any effect on these enzymes in membrane fractions from cultures of neonatal rat muscle mesenchymal cells, which do not calcify their matrix in vivo. These data suggest that 1,25-(OH)2D3 and 24,25-(OH)2D3 can directly affect chondrocyte membrane enzymes without genomic influence or protein synthesis and that membrane response depends on the stage of chondrocyte differentiation. Changes in PLA2 activity may change membrane fluidity and may be a mechanism by which the hormones affect cell membranes.

摘要

1,25 - 二羟基维生素D3 [1,25 - (OH)2D3] 和24,25 - (OH)2D3 对培养的肋软骨储备区和生长区软骨细胞产生的细胞膜及细胞外基质小泡的碱性磷酸酶(ALPase)和磷脂酶 - A2(PLA2)的比活性有不同影响。在本研究中,从汇合的软骨细胞培养物中分离出生长区软骨、储备区基质小泡和细胞膜,并在体外与激素孵育3小时和24小时。向生长区软骨(GC)基质小泡和细胞膜中添加1,25 - (OH)2D3 导致两个膜组分中ALPase和PLA2比活性呈剂量依赖性增加。向储备区软骨(RC)膜组分中添加24,25 - (OH)2D3 仅在10(-7) M和10(-8) M时刺激基质小泡ALPase,在10(-8) M时刺激细胞膜ALPase。然而,24,25 - (OH)2D3 抑制基质小泡和细胞膜PLA2活性。在3小时和24小时后均观察到维生素D代谢物的作用。两种激素代谢物对新生大鼠肌肉间充质细胞培养物的膜组分中的这些酶均无影响,新生大鼠肌肉间充质细胞在体内不会使其基质钙化。这些数据表明,1,25 - (OH)2D3 和24,25 - (OH)2D3 可直接影响软骨细胞膜酶,而无需基因组影响或蛋白质合成,且膜反应取决于软骨细胞分化阶段。PLA2活性的变化可能会改变膜流动性,可能是激素影响细胞膜的一种机制。

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