Parmacek M S, Decker M L, Lesch M, Samarel A M, Decker R S
Am J Physiol. 1986 Nov;251(5 Pt 1):C737-47. doi: 10.1152/ajpcell.1986.251.5.C737.
By use of a combined morphologic, immunocytochemical, and biochemical approach, this study demonstrates the changes in the lysosomal vacuolar apparatus that accompany thyroxine-induced cardiac hypertrophy. During the 1st wk of thyroxine administration, immunocytochemical studies revealed a decline in cathepsin D within many myocytes, but an increase within interstitial cells. These events transpired with only a modest rise in cathepsin D activity. During the 2nd wk, cathepsin D reappeared within most myocytes and continued to increase within the interstitial population and was associated with a general rise in lysosomal enzyme activity. These data demonstrate the importance of employing both immunocytochemical and biochemical approaches to evaluate the status of the lysosomal vacuolar apparatus, and suggests that the lysosomal vacuolar apparatus may be involved in the apparent remodeling that attends rapid cardiac growth, which may represent one component of the enhanced rates of proteolysis documented in this model of cardiac hypertrophy.
通过联合运用形态学、免疫细胞化学和生物化学方法,本研究证实了甲状腺素诱导心肌肥大过程中溶酶体空泡结构的变化。在给予甲状腺素的第1周,免疫细胞化学研究显示,许多心肌细胞内组织蛋白酶D含量下降,但间质细胞内含量增加。这些变化仅伴随着组织蛋白酶D活性的适度升高。在第2周,组织蛋白酶D重新出现在大多数心肌细胞内,并在间质细胞群体中持续增加,同时伴随着溶酶体酶活性的普遍升高。这些数据证明了采用免疫细胞化学和生物化学方法评估溶酶体空泡结构状态的重要性,并表明溶酶体空泡结构可能参与了快速心脏生长时的明显重塑过程,这可能是该心肌肥大模型中蛋白水解速率增强的一个组成部分。