MHV-A59 ENTERS POLARIZED MURINE EPITHELIAL-CELLS THROUGH THE APICAL SURFACE BUT IS RELEASED BASOLATERALLY

被引:20
作者
ROSSEN, JWA
VOORHOUT, WF
HORZINEK, MC
VANDERENDE, A
STROUS, GJAM
ROTTIER, PJM
机构
[1] UNIV UTRECHT, INST VIROL, DEPT IMMUNOL & INFECT DIS, 3584 CL UTRECHT, NETHERLANDS
[2] UNIV UTRECHT, FAC VET MED, DEPT FUNCT MORPHOL, 3584 CL UTRECHT, NETHERLANDS
[3] UNIV UTRECHT, SCH MED, CELL BIOL LAB, 3584 CX UTRECHT, NETHERLANDS
关键词
D O I
10.1006/viro.1995.1316
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coronaviruses have a marked tropism for epithelial cells. Entry and release of the porcine transmissible gastroenteritis virus (TGEV) is restricted to apical surfaces of polarized epithelial cells, as we have recently shown (J. W. A. Rossen, C. P. J. Bekker, W. F. Voorhout, G. J. A. M. Strous, A van der Ende, and P. J. M. Rottier, 1994, J. Virol. 68, 7966-7973). In this paper we analyze the interactions of mouse hepatitis coronavirus A59 (MHV-A59) with polarized murine kidney cells (mTAL) grown on permeable supports. After inoculation from the apical or basolateral side, virus entry was found to take place only through the apical membrane. The virus utilized a protein of the carcinoembryonic antigen family as its receptor. In contrast to TGEV, MHV-A59 was released preferentially from the basolateral plasma membrane domain, as evidenced by the accumulation of viral proteins and infectivity in the basolateral culture fluid as well as by electron microscopical observations. In the mouse, MHV initially replicates in the nasal epithelium before being disseminated throughout the body; the basolateral release of MHV from epithelial cells into the animal's circulation may be the first step in the establishment of a systemic infection. (C) 1995 Academic Press, Inc.
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页码:54 / 66
页数:13
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