Suppr超能文献

46 kDa甘露糖6-磷酸受体从高尔基体到晚期内体的循环路径与215 kDa M6PR的循环路径一致。

The recycling itinerary of the 46 kDa mannose 6-phosphate receptor--Golgi to late endosomes--coincides with that of the 215 kDa M6PR.

作者信息

Matovcik L M, Goodhouse J, Farquhar M G

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, CT.

出版信息

Eur J Cell Biol. 1990 Dec;53(2):203-11.

PMID:1964415
Abstract

The intracellular distribution and trafficking of the 46 kDa mannose 6-phosphate (M6PR) receptor has been investigated in rat Clone 9 hepatocytes and NRK cells and compared to that of the 215 kDa M6PR. Antibodies were generated to a synthetic peptide corresponding to the last 15 amino acids of the C-terminal cytoplasmic domain of the 46 kDa M6PR and used to localize it by immunofluorescence and immunoperoxidase labeling. At steady state the 46 kDa M6PR was concentrated at its presumptive sorting site in the Golgi complex, mainly in middle and trans cisternae. In cells treated with chloroquine or NH4Cl, the receptor was found in swollen multivesicular endosomes as well as in Golgi cisternae. When chloroquine-treated cells were double labeled with antibodies to both the 215 and 46 kDa M6PR, all of the endosomes which contained detectable 46 kDa also contained 215 kDa receptor. Thus, after weak base treatment, the 46 kDa receptor is located in a compartment which corresponds to the delivery site of the 215 kDa receptor, previously identified as a late endosome (Woods, J. W., J. Goodhouse, M. G. Farquhar, Eur. J. Cell Biol. 50, 132-143 (1989]. We conclude that the intracellular itinerary of the 46 kDa M6PR is similar to that of the 215 kDa M6PR in that both receptors cycle between the Golgi complex and the same population of late endosomes (prelysosomes). However, the distribution of the two receptors along the recycling route varies under identical conditions in these two cell types.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠克隆9肝细胞和NRK细胞中研究了46 kDa甘露糖6 - 磷酸(M6PR)受体的细胞内分布和运输,并与215 kDa M6PR进行了比较。针对与46 kDa M6PR C末端胞质结构域的最后15个氨基酸对应的合成肽产生抗体,并通过免疫荧光和免疫过氧化物酶标记来定位该受体。在稳态下,46 kDa M6PR集中在高尔基体复合体中其假定的分选位点,主要位于中间和反式潴泡中。在用氯喹或氯化铵处理的细胞中,该受体存在于肿胀的多泡内体以及高尔基体潴泡中。当用针对215 kDa和46 kDa M6PR的抗体对氯喹处理的细胞进行双重标记时,所有含有可检测到的46 kDa的内体也都含有215 kDa受体。因此,在弱碱处理后,46 kDa受体位于一个与215 kDa受体的递送位点相对应的区室中,先前已确定该递送位点为晚期内体(伍兹,J. W.,J. 古德豪斯,M. G. 法夸尔,《欧洲细胞生物学杂志》50,132 - 143(1989年))。我们得出结论,46 kDa M6PR的细胞内行程与215 kDa M6PR相似,即这两种受体都在高尔基体复合体和同一群晚期内体(前溶酶体)之间循环。然而,在这两种细胞类型中,在相同条件下这两种受体沿再循环途径的分布有所不同。(摘要截短于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验