Katsumata Osamu, Fujita-Yoshigaki Junko, Hara-Yokoyama Miki, Yanagishita Masaki, Furuyama Shunsuke, Sugiya Hiroshi
Department of Physiology and Research Institute of Oral Science, Nihon University School of Dentistry at Matsudo, 2-870-1 Sakaecho-Nishi, Matsudo, Chiba 271-8587, Japan.
Biochem Biophys Res Commun. 2007 Jun 15;357(4):1071-7. doi: 10.1016/j.bbrc.2007.04.053. Epub 2007 Apr 18.
Since it was reported that components of immature secretory granules (ISGs) are different from those of mature secretory granules (MSGs) in rat parotid acinar cells, we have been considering that components of secretory granules (SGs) change dynamically during granule maturation. As the first step to understand the mechanism of granule maturation, we separated low-density detergent-resistant membrane fractions (DRMs) from purified SGs of rat parotid gland. When SGs were lysed by the detergent Brij-58, syntaxin6 and VAMP4 were found in DRMs that were different from the GM1a-rich DRMs containing VAMP2. Because syntaxin6 and VAMP4 are known to be related to granule formation, we attempted to separate DRMs from ISGs. To enrich for ISGs, glands were removed from rats 5h after intraperitoneal injection of isoproterenol and used to purify the newly synthesized granules. Compared to mature granules prepared without injection, these newly formed granules were lower in density and contained higher concentrations of syntaxin6, VAMP4, and gamma-adaptin. This composition is consistent with the characterizations of ISGs. DRMs isolated from the newly formed granules were GM1a-rich and contained syntaxin6, VAMP4, and VAMP2 together. Thus, our findings suggest that syntaxin6 and VAMP4 associate with a GM1a-rich membrane microdomain during granule formation but enter a separate membrane microdomain before transport from granules during maturation.
自从有报道称大鼠腮腺腺泡细胞中未成熟分泌颗粒(ISGs)的成分与成熟分泌颗粒(MSGs)不同以来,我们一直在思考分泌颗粒(SGs)的成分在颗粒成熟过程中会动态变化。作为了解颗粒成熟机制的第一步,我们从大鼠腮腺纯化的SGs中分离出低密度去污剂抗性膜组分(DRMs)。当用去污剂Brij-58裂解SGs时,在DRMs中发现了 syntaxin6和VAMP4,它们与含有VAMP2的富含GM1a的DRMs不同。由于已知syntaxin6和VAMP4与颗粒形成有关,我们试图从ISGs中分离DRMs。为了富集ISGs,在腹腔注射异丙肾上腺素5小时后从大鼠身上取出腺体,用于纯化新合成的颗粒。与未注射制备的成熟颗粒相比,这些新形成的颗粒密度较低,含有较高浓度的syntaxin6、VAMP4和γ-衔接蛋白。这种组成与ISGs的特征一致。从新形成的颗粒中分离出的DRMs富含GM1a,并且一起含有syntaxin6、VAMP4和VAMP2。因此,我们的研究结果表明,syntaxin6和VAMP4在颗粒形成过程中与富含GM1a的膜微区相关联,但在成熟过程中从颗粒运输之前进入一个单独的膜微区。