Contribution of de novo protein synthesis to the hypertrophic effect of IGF-1 but not of thyroid hormones in adult ventricular cardiomyocytes

被引:11
作者
Bell, D [1 ]
McDermott, BJ [1 ]
机构
[1] Queens Univ Belfast, Dept Therapeut & Pharmacol, Cardiovasc Res Ctr, Sch Med, Belfast BT9 7BL, Antrim, North Ireland
关键词
hypertrophy; cardiomyocytes; growth factors; hormones; metabolism;
D O I
10.1023/A:1007014500965
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Enhanced expression of IGF-1 occurs in left ventricular hypertrophy (LVH) associated with systemic hypertension. Cardiac dysfunction accompanied by LVH is also observed in hyperthyroidism. Objective: to assess the relative contributions of de novo protein synthesis and attenuated protein degradation to increased protein mass associated with cardiomyocyte hypertrophy elicited by IGF-1 and thyroid hormones (tri-iodo thyronine T-3, and l-thyroxine T-4), respectively. Methods: total mass of protein, and both the incorporation, and removal of previously incorporated l-U-C-14-phenylalanine, indices of protein synthesis and degradation, respectively, were assessed in quiescent adult rat ventricular cardiomyocytes maintained in shortterm culture, and corrected for DNA content, as a index of cell number. Results: IGF-1 (1 pM-100 nM) increased cell protein significantly, maximally at 1 nM and by 38% above basal value after 24 h. T-3 (10 pM-2 mu M) and T-4 (10 pM-2 mu M) increased cell protein significantly maximally at 1 mu M and by 33.2 and 30.5%, respectively, above basal value. IGF-1 (less than or equal to 10 pM), T-3 (10 pM-2 mu M) and T-4 (10 pM-2 mu M) did not increase incorporation of l-U-C-14-phenylalanine above basal values. IGF-1 (100 pM-100 nM) increased incorporation of radiolabel significantly maximally at 100 nM and by 56%. T-4 (100 pM) and IGF-1 (10 pM), concentrations that did not stimulate de novo protein synthesis, attenuated the degradation of radiolabelled protein by 13.6 and 11.8%, respectively, compared to control values after 48 h. Conclusion: These data indicate that the acute hypertrophic response to (i) thyroid hormones cannot be attributed to initiation of de novo protein synthesis; (ii) IGF-1 comprises two components; the response elicited by IGF-1 (<10 pM) is independent of, while the response elicited by IGF-1 (>100 pM) is due to de novo protein synthesis.
引用
收藏
页码:113 / 124
页数:12
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