首页> 外文期刊>Journal of Biotechnology >Metalloproteinase activity is the sole factor responsible for the growth-promoting effect of conditioned medium in Trichoplusia ni insect cell cultures
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Metalloproteinase activity is the sole factor responsible for the growth-promoting effect of conditioned medium in Trichoplusia ni insect cell cultures

机译:金属蛋白酶活性是引起条件的培养基在毛滴虫昆虫细胞培养中促进生长的唯一因素

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摘要

Conditioned medium (CM) taken from a serum-free culture of Trichoplusia ni (BTI-Tn-5B1-4, High Five) cells on days 2 and 3, shortened the lagphase and increased the maximum cell density when added to T. ni cultures with low-inoculum cell density. Gel filtration fractions of CM, eluting at around 45kDa, stimulated cell proliferation even better than CM. A protein in the gel filtration fraction was identified by N-terminal amino acid sequencing as a proteinase, related to a snake venom metalloproteinase. Casein zymography showed, multiple metalloproteinase bands between 48 and 25kDa, as well as precursor forms above 48kDa. Metalloproteinase bands below the main band at 48kDa were autocatalytic degradation products. Metalloproteinase activity was the sole factor responsible for the growth stimulating effect of CM as shown by using the specific metalloproteinase inhibitor dl-thiorphan. Metalloproteinases have recently been shown to release growth factors from sequestering extracellular proteins. We propose that the metalloproteinase is involved in autocrine regulation of T. ni proliferation in serum-free media. In addition, a gel filtration fraction of CM, eluting at about 10kDa, inhibited cell growth. Apart from a lysozyme precursor protein and a cyclophilin-like protein, a kazal-type proteinase inhibitor could be identified in this fraction.
机译:在第2天和第3天从无毛滴虫(Trichoplusia ni ni)(BTI-Tn-5B1-4,高五)细胞的无血清培养物中提取的条件培养基(CM),当添加到T. ni培​​养物中时,缩短了延迟期并增加了最大细胞密度低眼菌细胞密度。 CM的凝胶过滤部分在45kDa左右洗脱时,甚至比CM更好地刺激了细胞增殖。通过N端氨基酸测序鉴定出凝胶过滤级分中的一种蛋白质为蛋白酶,与蛇毒金属蛋白酶有关。酪蛋白酶谱显示,在48至25kDa之间有多个金属蛋白酶带,以及在48kDa以上的前体形式。在主带以下的金属蛋白酶带(48kDa)是自催化降解产物。金属蛋白酶活性是引起CM的生长刺激作用的唯一因素,如使用特定的金属蛋白酶抑制剂dl-thiorphan所示。最近已显示金属蛋白酶从隔离细胞外蛋白中释放出生长因子。我们建议金属蛋白酶参与无血清培养基中T. ni增殖的自分泌调节。另外,以约10kDa洗脱的CM的凝胶过滤级分抑制细胞生长。除了溶菌酶前体蛋白和亲环蛋白样蛋白外,在该级分中还可以鉴定出一种kazal型蛋白酶抑制剂。

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