Max-Delbrück-Centrum für Molekulare Medizin and Leibniz-Institut für Molekulare Pharmakologie, Berlin, Germany.
Autophagy. 2010 Jan;6(1):158-9. doi: 10.4161/auto.6.1.10590.
Loss of the lysosomal chloride transport protein ClC-7 leads to complex phenotypes in mice and man, including osteopetrosis, accumulation of lysosomal storage material, and neurodegeneration. Using novel tissue-specific ClC-7 knockout mice, we have shown that upon loss of ClC-7, lysosomal degradation of endocytosed protein is slowed down and accumulation of autophagosomes occurs.
溶酶体氯离子转运蛋白 ClC-7 的缺失会导致小鼠和人类出现多种复杂表型,包括骨质硬化症、溶酶体贮积物的积累以及神经退行性变。利用新型组织特异性 ClC-7 敲除小鼠,我们发现 ClC-7 缺失后,内吞蛋白的溶酶体降解过程会减缓,自噬体的积累会发生。