Decker R S, Wildenthal K
Lab Invest. 1981 May;44(5):455-65.
Daily administration of L- or D-thyroxine for 1 week produced hypertrophy of the heart and atrophy of skeletal muscle and liver. The myocardial hypertrophy was accompanied by a rise in the activity of cathepsin D but not of cathepsin B; this was correlated with an increase in cathepsin-D-rich interstitial cells while the number of cathepsin-D-positive lysosomes in myocytes was decreased, as assessed from immunohistochemistry. In atrophying skeletal muscle (soleus and tibialis anterialis), large increases in the activities of cathepsins B and D were present. Immunohistochemical localization of cathepsin D revealed that in thyrotoxic striated muscle cells this acid proteinase had become localized diffusely in the paranuclear myoplasm. The atrophying liver of thyrotoxic rabbits also developed large increases in cathepsin D activity, but in this organ the increase was correlated with an increased number of cathepsin-D-positive secondary lysosomes without diffuse extralysosomal deposits. These observations indicate that changes in lysosomes and lysosomal enzyme activities elicited by thyrotoxicosis are tissue-specific. In some organs, the changes may be associated with net changes in protein balance or with tissue injury, but the exact functional significance of the lysosomal alterations remains uncertain.
连续1周每日给予L-甲状腺素或D-甲状腺素可导致心脏肥大以及骨骼肌和肝脏萎缩。心肌肥大伴随着组织蛋白酶D活性升高,但组织蛋白酶B活性未升高;根据免疫组织化学评估,这与富含组织蛋白酶D的间质细胞增多相关,而心肌细胞中组织蛋白酶D阳性溶酶体的数量减少。在萎缩的骨骼肌(比目鱼肌和胫前肌)中,组织蛋白酶B和D的活性大幅增加。组织蛋白酶D的免疫组织化学定位显示,在甲状腺毒症性横纹肌细胞中,这种酸性蛋白酶已弥散分布于核旁肌浆中。甲状腺毒症性兔萎缩的肝脏中组织蛋白酶D活性也大幅增加,但在该器官中,这种增加与组织蛋白酶D阳性次级溶酶体数量增加相关,而无弥散的溶酶体外沉积物。这些观察结果表明,甲状腺毒症引起的溶酶体和溶酶体酶活性变化具有组织特异性。在某些器官中,这些变化可能与蛋白质平衡的净变化或组织损伤有关,但溶酶体改变的确切功能意义仍不确定。