沙门氏菌
细胞生物学
溶酶体
生物
细胞内
液泡
吞噬作用
微生物学
吞噬体
基因敲除
细菌
基因
生物化学
酶
遗传学
细胞质
作者
Eun‐Ju Lee,Kwan-Sik Park,In-Sook Jeon,Jae‐Woon Choi,Sang-Jeon Lee,Hyun E. Choy,Ki‐Duk Song,Hak-Kyo Lee,Joong-Kook Choi
出处
期刊:Molecules and Cells
[Korean Society for Molecular and Cellular Biology]
日期:2016-06-22
卷期号:39 (7): 566-572
被引量:20
标识
DOI:10.14348/molcells.2016.0112
摘要
Lysosomes are cellular organelles containing diverse classes of catabolic enzymes that are implicated in diverse cellular processes including phagocytosis, autophagy, lipid transport, and aging. Lysosome-associated membrane proteins (LAMP-1 and LAMP-2) are major glycoproteins important for maintaining lysosomal integrity, pH, and catabolism. LAMP-1 and LAMP-2 are constitutively expressed in Salmonella-infected cells and are recruited to Salmonella-containing vacuoles (SCVs) as well as Salmonella-induced filaments (Sifs) that promote the survival and proliferation of the Salmonella. LAMP-3, also known as DC-LAMP/CD208, is a member of the LAMP family of proteins, but its role during Salmonella infection remains unclear. DNA microarray analysis identified LAMP-3 as one of the genes responding to LPS stimulation in THP-1 macrophage cells. Subsequent analyses reveal that LPS and Salmonella induced the expression of LAMP-3 at both the transcriptional and translational levels. Confocal Super resolution N-SIM imaging revealed that LAMP-3, like LAMP-2, shifts its localization from the cell surface to alongside Salmonella. Knockdown of LAMP-3 by specific siRNAs decreased the number of Salmonella recovered from the infected cells. Therefore, we conclude that LAMP-3 is induced by Salmonella infection and recruited to the Salmonella pathogen for intracellular proliferation.
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