Differentiation, extracellular matrix synthesis, and integrin assembly by Drosophila embryo cells cultured on vitronectin and laminin substrates.
Differentiation, extracellular matrix synthesis, and integrin assembly by Drosophila embryo cells cultured on vitronectin and laminin substrates.
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在玻连蛋白和层粘连蛋白基质上培养的果蝇胚胎细胞的分化、细胞外基质合成和整合素组装。
DOI:
10.1002/aja.1001990205
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发表时间:
1994
期刊:
影响因子:
--
通讯作者:
Fessler,JH
中科院分区:
文献类型:
--
作者:
Gullberg,D;Fessler,LI;Fessler,JH
Two contrasting substrates,Drosophilalaminin and human vitronectin, caused determined primaryDrosophilaembryo cells to follow alternate intermediate differentiation steps without affecting the final outcome of differentiation. Integrin αPS2βPS3was essential for the initial spreading of myocytes on vitronectin: focal contacts rich in βPS3integrins formed and were connected by actin‐ and myosin‐containing stress fibers. While αPS2βPS3was unnecessary for myotube formation on laminin, it was required for the subsequent change to a sarcomeric cytoarchitecture. The differentiating primary cultures synthesized integrins and assembled them into detergent‐insoluble, cytoskeleton‐associated complexes. Collagen IV, laminin, glutactin, papilin, and other other extracellular matrix proteins were made primarily by hemocytes and were secreted into the medium. Further differentiation within the cultures was influenced by secreted components and by later addition of vitronectin or bovine serum. Comparison of the differentiation of various cell types on the two substrates showed that vitronectin provided a selective advantage for the differentiation of myocytes, with enrichment over epithelia, epidermal cells, and neurites. © 1994 Wiley‐Liss, Inc.