TY - JOUR
T1 - The effect of ethanol on asialoglycoprotein receptor-mediated phagocytosis of apoptotic cells by rat hepatocytes
AU - McVicker, Benita L.
AU - Tuma, Dean J.
AU - Kubik, Jacy A.
AU - Hindemith, Agnes M.
AU - Baldwin, Cheryl R.
AU - Casey, Carol A.
N1 - Funding Information:
Abbreviations: ASGP-R, asialoglycoprotein receptor; GalNAc, N-acetylgalactosamine; TAMRA, 5-6-carboxytetramethyl-rhodamine-succinimidyl-ester; FITC, fluorescein isothiocyanate; ASOR, asialoorosomucoid; R1, gated hepatocyte population region. From the Liver Study Unit, Department of Veterans Affairs Medical Center, and the Departments of Internal Medicine and Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE. Received March 7, 2002; accepted September 18, 2002. Supported by a grant (AA07846) from the National Institute on Alcohol Abuse and Alcoholism, the Department of Veterans Affairs, and the Alcohol Beverage Medical Research Foundation. Address reprint requests to: Dr. Carol A. Casey, Liver Study Unit, Department of Veterans Affairs Medical Center, 4101 Woolworth Ave., Omaha, NE 68105. E-mail: [email protected]; fax: 402-449-0604. Copyright © 2002 by the American Association for the Study of Liver Diseases. 0270-9139/02/3606-0024$35.00/0 doi:10.1053/jhep.2002.37137
Funding Information:
Acknowledgment: The authors thank Dr. Charles Kuszynski and Linda Wilkie from the Cell Analysis Core Research Facility in the Department of Pathology and Microbiology at the University of Nebraska Medical Center for their expert consultation and technical support. The authors also are grateful to Janice Taylor of the Confocal Laser Scanning Microscope Core Facility at the University of Nebraska Medical Center, which is supported by the Nebraska Research Initiative, for providing assistance with confocal microscopy.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - Apoptotic cell death is a well-defined process that is controlled by intrinsic cellular mechanisms followed by the generation of apoptotic bodies and their subsequent rapid elimination through the action of phagocytic cells. Within the liver, the asialoglycoprotein receptor (ASGP-R) has been shown to be involved in the phagocytosis of apoptotic hepatocytes, as well as altered cellular endocytic events after ethanol administration. The goal of the present study was to further clarify the capacity of ASGP-R to phagocytose apoptotic cells in relationship to the damaging events that occur with alcohol consumption. For these experiments, we used an in vitro suspension assay coupled with flow cytometry to measure apoptotic cell engulfment by rat hepatocytes after chronic ethanol administration. The results of this assay indicated that the phagocytosis of apoptotic cells was decreased significandy (30% to 42%, P < .05) in the presence of antibody specific for ASGP-R as well as the introduction of competing sugars in the media. In addition, uptake of apoptotic cells was impaired by 40% to 60% (P < .05) in cells obtained from ethanol-fed animals as compared with controls. In conclusion, the ASGP-R is involved in the recognition and uptake of apoptotic cells and this process is altered significantly by ethanol treatment. These findings may play a role in a better understanding of the clinical manifestations of alcohol-induced liver injury as altered uptake of apoptotic cells via ASGP-R may result in the release of proinflammatory mediators, the introduction of autoimmune responses, and inflammatory injury to the tissue.
AB - Apoptotic cell death is a well-defined process that is controlled by intrinsic cellular mechanisms followed by the generation of apoptotic bodies and their subsequent rapid elimination through the action of phagocytic cells. Within the liver, the asialoglycoprotein receptor (ASGP-R) has been shown to be involved in the phagocytosis of apoptotic hepatocytes, as well as altered cellular endocytic events after ethanol administration. The goal of the present study was to further clarify the capacity of ASGP-R to phagocytose apoptotic cells in relationship to the damaging events that occur with alcohol consumption. For these experiments, we used an in vitro suspension assay coupled with flow cytometry to measure apoptotic cell engulfment by rat hepatocytes after chronic ethanol administration. The results of this assay indicated that the phagocytosis of apoptotic cells was decreased significandy (30% to 42%, P < .05) in the presence of antibody specific for ASGP-R as well as the introduction of competing sugars in the media. In addition, uptake of apoptotic cells was impaired by 40% to 60% (P < .05) in cells obtained from ethanol-fed animals as compared with controls. In conclusion, the ASGP-R is involved in the recognition and uptake of apoptotic cells and this process is altered significantly by ethanol treatment. These findings may play a role in a better understanding of the clinical manifestations of alcohol-induced liver injury as altered uptake of apoptotic cells via ASGP-R may result in the release of proinflammatory mediators, the introduction of autoimmune responses, and inflammatory injury to the tissue.
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U2 - 10.1053/jhep.2002.37137
DO - 10.1053/jhep.2002.37137
M3 - Article
C2 - 12447874
AN - SCOPUS:0036895297
SN - 0270-9139
VL - 36
SP - 1478
EP - 1487
JO - Hepatology
JF - Hepatology
IS - 6
ER -