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磷脂酰肌醇3激酶激活在成人心室心肌细胞肥大生长中的作用

Role of phosphatidylinositol 3-kinase activation in the hypertrophic growth of adult ventricular cardiomyocytes.

作者信息

Schlüter K D, Goldberg Y, Taimor G, Schäfer M, Piper H M

机构信息

Physiologisches Institut, Universität Giessen, Giessen, Germany.

出版信息

Cardiovasc Res. 1998 Oct;40(1):174-81. doi: 10.1016/s0008-6363(98)00171-0.

Abstract

OBJECTIVE

The present study investigated whether activation of phosphatidylinositol 3-kinase (PI3-kinase) is involved in the stimulation of hypertrophic growth of adult ventricular cardiomyocytes under alpha- or beta-adrenoceptor stimulation.

METHODS

Adult ventricular rat cardiomyocytes were used either directly after isolation (day 1 culture) or after cultivation for 6 days in presence of 20% fetal calf serum (day 7 culture). PI3-kinase activity was determined in extracts of cardiomyocytes after immunoprecipitation with an antibody against the p85 subunit of PI3-kinase. The influence of PI3-kinase inhibition on myocardial growth was determined using the specific PI3-kinase inhibitors wortmannin and LY294002.

RESULTS

In day 1 cultures alpha-adrenoceptor stimulation, but not beta-adrenoceptor stimulation caused activation of PI3-kinase. In response to alpha-adrenoceptor stimulation but not beta-adrenoceptor stimulation an acceleration of protein synthesis (incorporation of 14C-phenylalanine) and an increase in the total masses of cellular protein and RNA was observed. In these cultures inhibition of PI3-kinase attenuated the acceleration of protein synthesis and the increase in cellular masses of protein or RNA in response to alpha-adrenoceptor stimulation. In day 7 cultures alpha- and beta-adrenoceptor stimulation caused activation of PI3-kinase and increased protein synthesis. In these cultures inhibition of PI3-kinase attenuated the growth response to alpha- and beta-adrenoceptor stimulation.

CONCLUSIONS

PI3-kinase activation via protein kinase C-dependent or cAMP-dependent pathways is required for hypertrophic growth of adult cardiomyocytes.

摘要

目的

本研究调查磷脂酰肌醇3激酶(PI3激酶)的激活是否参与α或β肾上腺素能受体刺激下成年心室心肌细胞肥大生长的刺激过程。

方法

成年大鼠心室肌细胞在分离后(第1天培养)或在含有20%胎牛血清的条件下培养6天(第7天培养)后直接使用。用抗PI3激酶p85亚基的抗体进行免疫沉淀后,测定心肌细胞提取物中的PI3激酶活性。使用特异性PI3激酶抑制剂渥曼青霉素和LY294002确定PI3激酶抑制对心肌生长的影响。

结果

在第1天培养物中,α肾上腺素能受体刺激而非β肾上腺素能受体刺激导致PI3激酶激活。响应α肾上腺素能受体刺激而非β肾上腺素能受体刺激,观察到蛋白质合成加速(14C-苯丙氨酸掺入)以及细胞蛋白质和RNA总量增加。在这些培养物中,PI3激酶的抑制减弱了响应α肾上腺素能受体刺激时蛋白质合成的加速以及蛋白质或RNA细胞质量的增加。在第7天培养物中,α和β肾上腺素能受体刺激导致PI3激酶激活并增加蛋白质合成。在这些培养物中,PI3激酶的抑制减弱了对α和β肾上腺素能受体刺激的生长反应。

结论

成年心肌细胞肥大生长需要通过蛋白激酶C依赖性或cAMP依赖性途径激活PI3激酶。

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