Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation

Objective To explore the role and mechanism of hepatocytes in inhibiting bacterial proliferation by phagocytizing bacteria directly and mediating the expression of antibacterial proteins indirectly. Methods Cellular model of Escherichia coli (E.coli) infection was established in normal murine hepato...

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Main Authors: MA Wei, SHU Junjie, CHEN Diyou
Format: Article
Language:zho
Published: Editorial Office of Journal of Army Medical University 2023-11-01
Series:陆军军医大学学报
Subjects:
Online Access:http://aammt.tmmu.edu.cn/html/202306111.htm
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author MA Wei
MA Wei
SHU Junjie
CHEN Diyou
CHEN Diyou
author_facet MA Wei
MA Wei
SHU Junjie
CHEN Diyou
CHEN Diyou
author_sort MA Wei
collection DOAJ
description Objective To explore the role and mechanism of hepatocytes in inhibiting bacterial proliferation by phagocytizing bacteria directly and mediating the expression of antibacterial proteins indirectly. Methods Cellular model of Escherichia coli (E.coli) infection was established in normal murine hepatocyte line FL83B and mouse Kupffer cells to determine the effects of the cells on the proliferation of bacteria. After the bacteria were co-cultured with Kupffer/FL83B cells and the 6-, 12-, and 24-hour supernatants, respectively, the lethality of E. coli was determined for the direct bacteriostatic effect of the hepatocytes. The phagocytizing ability of FL83B cells were measured with phagocytosis reagent kit. qRT-PCR and Western blotting were employed to detect the expression of related molecules at mRNA and protein levels. Results When the hepatocyte were incubated with E. coli, FL83B cells, as Kupffer cells, could directly inhibit the proliferation of the bacteria (P < 0.05) and maintained a high survival rate at same time. Phagocytic function test showed that FL83B cells could directly phagocytize bacterial particles. Compared with the FL83B cells without E. coli infection, the mRNA levels of phagocytosis-related genes Fcgr1, Marco, Cdc42, and RhoB were increased, that of antigen presentation related gene β2M was also upregulated, the NF-κB, MAPK, and STAT3 signaling pathways were activated, and the protein levels of antibacterial-related proteins iNOS, NOX2, and RhoB were also enhanced in the cells after infection (all P < 0.05). Conclusion Mouse FL83B hepatocytes possess the ability to inhibit bacteria through direct phagocytosis and indirect upregulation of antibacterial-related proteins.
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spelling doaj.art-5bd44c54c9144f2ba39f877a99864eda2023-11-10T03:29:20ZzhoEditorial Office of Journal of Army Medical University陆军军医大学学报2097-09272023-11-0145212206221310.16016/j.2097-0927.202306111Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferationMA Wei0MA Wei1SHU Junjie2CHEN Diyou3CHEN Diyou4Department of Cell Biology, College of Basic Medical Sciences, Army Medical University (Third Military Medical University), Chongqing, 400038Department of Wound Infection and Drug, Army Medical Center of PLA, Chongqing, 400042, ChinaDepartment of Wound Infection and Drug, Army Medical Center of PLA, Chongqing, 400042, ChinaDepartment of Radiology, Army Medical Center of PLA, Chongqing, 400042, ChinaDepartment of Military Traffic Injury Prevention and Treatment, Army Medical Center of PLA, Chongqing, 400042, ChinaObjective To explore the role and mechanism of hepatocytes in inhibiting bacterial proliferation by phagocytizing bacteria directly and mediating the expression of antibacterial proteins indirectly. Methods Cellular model of Escherichia coli (E.coli) infection was established in normal murine hepatocyte line FL83B and mouse Kupffer cells to determine the effects of the cells on the proliferation of bacteria. After the bacteria were co-cultured with Kupffer/FL83B cells and the 6-, 12-, and 24-hour supernatants, respectively, the lethality of E. coli was determined for the direct bacteriostatic effect of the hepatocytes. The phagocytizing ability of FL83B cells were measured with phagocytosis reagent kit. qRT-PCR and Western blotting were employed to detect the expression of related molecules at mRNA and protein levels. Results When the hepatocyte were incubated with E. coli, FL83B cells, as Kupffer cells, could directly inhibit the proliferation of the bacteria (P < 0.05) and maintained a high survival rate at same time. Phagocytic function test showed that FL83B cells could directly phagocytize bacterial particles. Compared with the FL83B cells without E. coli infection, the mRNA levels of phagocytosis-related genes Fcgr1, Marco, Cdc42, and RhoB were increased, that of antigen presentation related gene β2M was also upregulated, the NF-κB, MAPK, and STAT3 signaling pathways were activated, and the protein levels of antibacterial-related proteins iNOS, NOX2, and RhoB were also enhanced in the cells after infection (all P < 0.05). Conclusion Mouse FL83B hepatocytes possess the ability to inhibit bacteria through direct phagocytosis and indirect upregulation of antibacterial-related proteins. http://aammt.tmmu.edu.cn/html/202306111.htmhepatocytesbacterial infectionphagocytosis
spellingShingle MA Wei
MA Wei
SHU Junjie
CHEN Diyou
CHEN Diyou
Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
陆军军医大学学报
hepatocytes
bacterial infection
phagocytosis
title Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
title_full Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
title_fullStr Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
title_full_unstemmed Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
title_short Inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
title_sort inhibitory effect and underlying mechanism of hepatocytes on bacterial proliferation
topic hepatocytes
bacterial infection
phagocytosis
url http://aammt.tmmu.edu.cn/html/202306111.htm
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AT shujunjie inhibitoryeffectandunderlyingmechanismofhepatocytesonbacterialproliferation
AT chendiyou inhibitoryeffectandunderlyingmechanismofhepatocytesonbacterialproliferation
AT chendiyou inhibitoryeffectandunderlyingmechanismofhepatocytesonbacterialproliferation