Polla B S, Healy A M, Byrne M, Krane S M
Department of Medicine, Harvard Medical School, Boston, Massachusetts 02114.
J Clin Invest. 1987 Oct;80(4):962-9. doi: 10.1172/JCI113189.
Interactions of cells with components of the extracellular matrix can modulate cellular functions. We measured binding of a major matrix protein to U937 cells, a human promonocytic line. Radioiodinated type I or type III human collagen was bound only to U937 cells differentiated to a more mature phenotype with 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3). Binding was observed at 4 degrees C and was saturable; Scatchard analysis of the binding to 1,25-(OH)2D3-pretreated U937 cells indicated a single class of high-affinity binding sites. Preincubation of U937 cells with interferon gamma did not induce collagen binding. Collagen binding did not appear to be dependent on fibronectin binding. Surface proteins of U937 cells were 125I labeled and cell membrane proteins resolved by affinity chromatography on collagen-Sepharose. Major specifically labeled bands of 180, 155, and 125 kD were identified in membrane fractions from 1,25-(OH)2D3-pretreated U937 cells only. 1,25-(OH)2D3 appears to specifically regulate collagen binding to monocyte precursors.
细胞与细胞外基质成分的相互作用能够调节细胞功能。我们检测了一种主要基质蛋白与U937细胞(一种人原单核细胞系)的结合情况。放射性碘化的I型或III型人胶原蛋白仅与经1,25 - 二羟基维生素D3(1,25-(OH)2D3)诱导分化为更成熟表型的U937细胞结合。在4℃时可观察到结合,且具有饱和性;对与1,25-(OH)2D3预处理的U937细胞的结合进行Scatchard分析表明存在一类单一的高亲和力结合位点。用γ干扰素对U937细胞进行预孵育不会诱导胶原蛋白结合。胶原蛋白结合似乎不依赖于纤连蛋白结合。用125I标记U937细胞的表面蛋白,并通过在胶原 - 琼脂糖上进行亲和层析分离细胞膜蛋白。仅在来自1,25-(OH)2D3预处理的U937细胞的膜组分中鉴定出180、155和125 kD的主要特异性标记条带。1,25-(OH)2D3似乎特异性调节胶原蛋白与单核细胞前体的结合。