Hepatocyte turnover during resolution of a transient hepadnaviral infection

被引:138
作者
Summers, J [1 ]
Jilbert, AR
Yang, WG
Aldrich, CE
Saputelli, J
Litwin, S
Toll, E
Mason, WS
机构
[1] Univ New Mexico, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[2] Univ Adelaide, Inst Med & Vet Sci, Adelaide, SA 5000, Australia
[3] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
关键词
D O I
10.1073/pnas.1635109100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We estimated the amount of hepatocyte turnover in the livers of three woodchucks undergoing clearance of a transient woodchuck hepatitis infection by determining the fate of integrated viral DNA as a genetic marker of the infected cell population. Integrated viral DNA was found to persist in liver tissue from recovered animals at essentially undiminished levels of 1 viral genome per 1,000-3,000 liver cells, suggesting that the hepatocytes in the recovered liver were derived primarily from the infected cell population. We determined the single and multicopy distribution of distinct viral cell junctions isolated from small pieces of liver after clearance of the infection to determine the cumulative amount of hepatocyte proliferation that had occurred during recovery. We estimated that proliferation was equivalent to a minimum of 0.7-1 complete random turnovers of the hepatocyte population of the liver. Our results indicated that during resolution of the transient infections a large fraction of the infected hepatocyte population was killed and replaced by hepatocyte cell division.
引用
收藏
页码:11652 / 11659
页数:8
相关论文
共 41 条
[1]  
CARP NZ, 1991, LAB ANIM SCI, V41, P474
[2]   Inhibition of hepatitis B virus replication during adenovirus and cytomegalovirus infections in transgenic mice [J].
Cavanaugh, VJ ;
Guidotti, LG ;
Chisari, FV .
JOURNAL OF VIROLOGY, 1998, 72 (04) :2630-2637
[3]   Interleukin-12 inhibits hepatitis B virus replication in transgenic mice [J].
Cavanaugh, VJ ;
Guidotti, LG ;
Chisari, FV .
JOURNAL OF VIROLOGY, 1997, 71 (04) :3236-3243
[4]   IMMUNOLOGICAL ASPECTS OF HEPATITIS-B VIRUS-INFECTION [J].
EDGINGTON, TS ;
CHISARI, FV .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1975, 270 (02) :213-227
[5]   Entecavir therapy combined with DNA vaccination for persistent duck hepatitis B virus infection [J].
Foster, WK ;
Miller, DS ;
Marion, PL ;
Colonno, RJ ;
Kotlarski, I ;
Jilbert, AR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (08) :2624-2635
[6]   EVIDENCE THAT HEPATOCYTE TURNOVER IS REQUIRED FOR RAPID CLEARANCE OF DUCK HEPATITIS-B VIRUS DURING ANTIVIRAL THERAPY OF CHRONICALLY INFECTED DUCKS [J].
FOUREL, I ;
CULLEN, JM ;
SAPUTELLI, J ;
ALDRICH, CE ;
SCHAFFER, P ;
AVERETT, DR ;
PUGH, J ;
MASON, WS .
JOURNAL OF VIROLOGY, 1994, 68 (12) :8321-8330
[7]   NUCLEOTIDE-SEQUENCE OF A CLONED WOODCHUCK HEPATITIS-VIRUS GENOME - COMPARISON WITH THE HEPATITIS-B VIRUS SEQUENCE [J].
GALIBERT, F ;
CHEN, TN ;
MANDART, E .
JOURNAL OF VIROLOGY, 1982, 41 (01) :51-65
[8]  
Ganem D., 2001, FIELDS VIROLOGY, V2, P2923
[9]   Efficacy of the carbocyclic 2′-deoxyguanosine nucleoside BMS-200475 in the woodchuck model of hepatitis B virus infection [J].
Genovesi, EV ;
Lamb, L ;
Medina, I ;
Taylor, D ;
Seifer, M ;
Innaimo, S ;
Colonno, RJ ;
Standring, DN ;
Clark, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (12) :3209-3217
[10]  
Guidotti LG, 1999, CURR OPIN MICROBIOL, V2, P388