Braulke T, Hasilik A, von Figura K
Biochemie II der Universität Göttingen.
Biol Chem Hoppe Seyler. 1988 Jun;369(6):441-9. doi: 10.1515/bchm3.1988.369.1.441.
The transport of newly synthesized cathepsin D in fibroblasts at 16-28 degrees C was compared to that at 37 degrees C. At 37 degrees C newly synthesized cathepsin D passes the trans Golgi within 30-60 min, becomes segregated from the secretory route into prelysosomal organelles within 1-2 h and processed to mature forms in dense lysosomes within 1.5-3 h after synthesis. The small fraction of cathepsin D that escapes transport into lysosomes is secreted within less than 2 h. At 16-28 degrees C the transport of cathepsin D to lysosomes is inhibited in a temperature-dependent manner. At 16-28 degrees C cathepsin D precursors are slowly transported to the trans Golgi. The cathepsin D precursors accumulate at a site that is in continuity with the secretory pathway and located within or distal of the trans Golgi and proximal to the site where cathepsin D precursors leave the secretory pathway as complexes with mannose 6-phosphate receptors. The arrest at this site is not complete. The receptor-dependent segregation of the cathepsin D precursors released from the block is impaired at less than or equal to 26 degrees C. The inhibition of segregation results in an increased, albeit retarded secretion of cathepsin D. The fraction of cathepsin D precursors that is segregated from the secretory pathway encounters a further low temperature block in prelysosomal organelles. There cathepsin D precursors are proteolytically processed to an intermediate form, which accumulates transiently.(ABSTRACT TRUNCATED AT 250 WORDS)
将成纤维细胞在16 - 28摄氏度时新合成的组织蛋白酶D的运输与在37摄氏度时的运输进行了比较。在37摄氏度时,新合成的组织蛋白酶D在30 - 60分钟内通过反式高尔基体,在1 - 2小时内从分泌途径分离进入前溶酶体细胞器,并在合成后1.5 - 3小时内在致密溶酶体中加工成成熟形式。少量未运输到溶酶体的组织蛋白酶D在不到2小时内被分泌。在16 - 28摄氏度时,组织蛋白酶D向溶酶体的运输以温度依赖的方式受到抑制。在16 - 28摄氏度时,组织蛋白酶D前体缓慢运输到反式高尔基体。组织蛋白酶D前体在一个与分泌途径连续的位点积累,该位点位于反式高尔基体内部或远端,且靠近组织蛋白酶D前体与甘露糖6 - 磷酸受体形成复合物离开分泌途径的位点。在这个位点的停滞并不完全。在小于或等于26摄氏度时,从阻滞中释放的组织蛋白酶D前体的受体依赖性分离受损。分离的抑制导致组织蛋白酶D的分泌增加,尽管有所延迟。从分泌途径分离的组织蛋白酶D前体部分在溶酶体前细胞器中遇到进一步的低温阻滞。在那里,组织蛋白酶D前体被蛋白水解加工成一种中间形式,并短暂积累。(摘要截断于250字)