首页> 外文期刊>European Journal of Histochemistry >Isolation of rat hepatocytes for pharmacological studies on metabotropic glutamate receptor (mGluR) subtype 5: a comparison between collagenase I versus collagenase IV
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Isolation of rat hepatocytes for pharmacological studies on metabotropic glutamate receptor (mGluR) subtype 5: a comparison between collagenase I versus collagenase IV

机译:代表胶质谷氨酸受体(MGLUR)亚型5:胶原酶I与胶原酶IV的比较分离对药理学研究的分离

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Isolated hepatocytes can be obtained from the liver by collagenase infusion, a procedure that could affect cell isolation as well as the integrity of membrane receptors. In this respect we compared metabotropic glutamate subtype 5 receptor (mGluR5) protein expression and activity in rat hepatocytes isolated by two collagenases, type I and type IV. Hepatocytes were isolated from male Wistar rats (200-250 g) using collagenase I or collagenase IV and after isolation, viability and morphology of rat hepatocytes were assessed measuring mGluR5 protein expression by Western blot analyses. mGluR5 activation was evaluated by inositol-1-phosphate (IP-1) accumulation after treatment with the mGluR5 orthosteric agonist ACPD or the selective antagonist MPEP. No difference in cellular viability and morphology was observed using collagenase I when compared with collagenase IV. An increase in mGluR5 protein expression was observed in hepatocytes isolated using collagenase IV with respect to collagenase I. Moreover, hepatocytes treated with ACPD and with MPEP presented higher levels of IP-1 when isolated using collagenase IV compared to collagenase I. These results indicate that collagenase IV better preserves the activity of surface proteins such as mGluR5 in isolated rat hepatocytes, an in vitro model useful to reduce the use of experimental animals, in line with the 3R ethical framework.
机译:可以通过胶原酶输注从肝脏获得分离的肝细胞,这是一种可能影响细胞分离的程序以及膜受体的完整性。在这方面,我们将代谢谷氨酸亚型5受体(MgLuR5)蛋白表达和在大鼠肝细胞中进行比较,在由两种胶原酶,I型和I型分离的大鼠肝细胞中。使用胶原酶I或胶原蛋白酶IV与雄性Wistar大鼠(200-250g)分离肝细胞,并在分离后,通过Western印迹分析评估大鼠肝细胞的活力和形态测量MgluR5蛋白表达。用MGLUR5倒药剂ACPD或选择性拮抗剂MPEP治疗后,通过肌醇-1-磷酸(IP-1)积累评估MGLUR5活化。与胶原酶IV相比,使用胶原酶I观察细胞活力和形态的差异。在使用胶原酶I相对于胶原酶I相对于胶原酶I相对于胶原蛋白酶I分离出的肝细胞中观察到MGLUR5蛋白表达的增加。用胶原酶IV与胶原酶I相比,用ACPD处理的肝细胞和MPEP呈现较高水平的IP-1。这些结果表明胶原酶IV更好地保留了表面蛋白如Mglure5在分离的大鼠肝细胞中的活性,这是一种用于减少使用实验动物的体外模型,符合3R伦理框架。

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