Glick J M, Rothblat G H
Biochim Biophys Acta. 1980 Apr 18;618(1):163-72. doi: 10.1016/0005-2760(80)90063-6.
Cultured cells derived from the stromal-vascular fraction of rat epididymal adipose tissue have been used to study the release of lipoprotein lipase in response to heparin. In the presence of heparin, lipoprotein lipase appeared in the medium biphasically, with an initial rapid rise followed by a slower linear release. The initial increase in activity in the medium was paralleled by a decrease in cell-associated activity. Over the course of the slower phase of release, cell-associated lipoprotein lipase levels remained constant. Treatment of cultures with cycloheximide or 2-deoxyglucose eliminated the second phase of release as well as cell-associated lipoprotein lipase activity. Treatment of cultures with Colcemid decreased the second phase of release but increased cell-associated lipoprotein lipase activity. These data suggest that exposure to heparin results in a rapid release of pre-formed enzyme and that continued release is dependent on both protein synthesis and transport of the enzyme to the cell surface.
源自大鼠附睾脂肪组织基质血管部分的培养细胞已被用于研究脂蛋白脂肪酶对肝素的反应释放情况。在肝素存在的情况下,脂蛋白脂肪酶在培养基中呈双相出现,最初迅速上升,随后是较慢的线性释放。培养基中活性的最初增加与细胞相关活性的降低相平行。在释放的较慢阶段,细胞相关的脂蛋白脂肪酶水平保持恒定。用环己酰亚胺或2-脱氧葡萄糖处理培养物消除了释放的第二阶段以及细胞相关的脂蛋白脂肪酶活性。用秋水仙酰胺处理培养物减少了释放的第二阶段,但增加了细胞相关的脂蛋白脂肪酶活性。这些数据表明,暴露于肝素会导致预先形成的酶快速释放,并且持续释放依赖于蛋白质合成以及酶向细胞表面的转运。