Experimental Papers
Copyright ©The Author(s) 1996. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 15, 1996; 2(4): 212-214
Published online Dec 15, 1996. doi: 10.3748/wjg.v2.i4.212
Mechanism of cryopreserved porcine hepatocyte xenotransplantation in treating acute hepatic failure
Cong Lin, Kuan-Yong Hou, Wen-Xiu Zhang, Jing-Ning Lu, Xiao-Si Zhou, Yan-Dao Gong, Xiao-Lang Ding, Xiu-Fang Zhang, Nan-Ming Zhao
Cong Lin, Kuan-Yong Hou, Wen-Xiu Zhang, Jing-Ning Lu, Xiao-Si Zhou, Department of Surgery, Third Hospital, Beijing Medical University, Beijing 100083, China
Yan-Dao Gong, Xiao-Lang Ding, Xiu-Fang Zhang, Nan-Ming Zhao, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing 100084, China
Author contributions: All authors contributed equally to the work.
Supported by The Science Foundation of Chinese Ministry of Health, No. 942194; and the National Natural Science Foundation of China, No. 59493208.
Correspondence to: Dr. Cong Lin, Department of Surgery, Third Hospital, Beijing Medical University, Beijing 100083, China
Telephone: +86-10-62017691-2547
Received: July 30, 1996
Revised: September 12, 1996
Accepted: October 22, 1996
Published online: December 15, 1996
Abstract

AIM: To study the effect of hypothermia on structure of membrane proteins of pig hepatocytes and the mechanism of transplantation of cryopreserved porcine hepatocytes in treating acute hepatic failure in Wistar rats.

METHODS: Isolated porcine hepatocytes were cryopreserved in liquid nitrogen for 150 d and then transplanted to the rat abdominal cavity. Three days later, 80% of rat liver by weight was resected. Conformation of membrane proteins of the porcine hepatocytes, liver function and weight of the remaining liver in the rats were measured.

RESULTS: Viability of the cryopreserved hepatocytes was 78%. Light and electron microscopy showed that the hepatocytes were morphologically intact. The cells were rich in glycogen and glucose-6-phosphatase. The α-helix content in the membrane proteins of fresh cells was 48%. After freezing the cells, the content was increased to 59.5%. Survival rate of rats in the transplanted group was 16/17, significantly higher than 3/9 in the control group (P = 0.0022). However, there were no significant differences in the weight of the remaining liver or indices of liver function between the two groups.

CONCLUSION: Transplant of frozen porcine hepatocytes is effective in treating acute hepatic failure. The mechanism is suggested to be a result of multiple effects. Hypothermia could increase α-helix content in the cellular membrane proteins, which might be related to the report that hypothermia was able to reduce the immunogenicity of the transplanted tissues and cells.

Keywords: Liver failure, acute; Cryopreservation, Liver/cytology; Transplantation, Heterologous; Membrane proteins