INTEGRIN ALPHA-V-BETA-5 SELECTIVELY PROMOTES ADENOVIRUS-MEDIATED CELL-MEMBRANE PERMEABILIZATION

被引:357
作者
WICKHAM, TJ [1 ]
FILARDO, EJ [1 ]
CHERESH, DA [1 ]
NEMEROW, GR [1 ]
机构
[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
关键词
D O I
10.1083/jcb.127.1.257
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human adenovirus type 2 (Ad2) enters host cells by receptor-mediated endocytosis, an event mediated by the virus penton base binding to cell surface integrins alpha v beta 3 and alpha v beta 5. While both alpha v integrins promote virus internalization, alpha v beta 5 is involved in the subsequent event of membrane permeabilization. Cells transfected with the beta 5 or beta 3 subunit, expressing either alpha v beta 5 and alpha v beta 3, respectively, were capable of supporting Ad2 infection to varying degrees. In this case, cells expressing alpha v beta 5 were significantly more susceptible to Ad2-induced membrane permeabilization, as well as to Ad2 infection, than cells expressing alpha v beta 3. Adenovirus-mediated gene delivery was also more efficient in cells expressing alpha v beta 5. These results suggest that the interaction of alpha v beta 5 with Ad2 penton base facilitates the subsequent step of virus penetration into the cell. These studies provide evidence for the involvement of a cellular receptor in virus-mediated membrane permeabilization and suggest a novel biological role for integrin alpha v beta 5 in the infectious pathway of a human adenovirus.
引用
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页码:257 / 264
页数:8
相关论文
共 38 条
[1]   MUTATIONS THAT ALTER AN ARG-GLY-ASP (RGD) SEQUENCE IN THE ADENOVIRUS TYPE-2 PENTON BASE PROTEIN ABOLISH ITS CELL-ROUNDING ACTIVITY AND DELAY VIRUS REPRODUCTION IN FLAT CELLS [J].
BAI, M ;
HARFE, B ;
FREIMUTH, P .
JOURNAL OF VIROLOGY, 1993, 67 (09) :5198-5205
[2]   PH-DEPENDENT LYSIS OF LIPOSOMES BY ADENOVIRUS [J].
BLUMENTHAL, R ;
SETH, P ;
WILLINGHAM, MC ;
PASTAN, I .
BIOCHEMISTRY, 1986, 25 (08) :2231-2237
[3]   INFECTIONS IN 18,000 INFANTS AND CHILDREN IN A CONTROLLED STUDY OF RESPIRATORY TRACT DISEASE .I. ADENOVIRUS PATHOGENICITY IN RELATION TO SEROLOGIC TYPE AND ILLNESS SYNDROME [J].
BRANDT, CD ;
KIM, HW ;
VARGOSKO, AJ ;
JEFFRIES, BC ;
ARROBIO, JO ;
RINDGE, B ;
PARROTT, RH ;
CHANOCK, RM .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1969, 90 (06) :484-&
[4]   EARLY EVENTS IN INTERACTION OF ADENOVIRUSES WITH HELA CELLS .1. PENETRATION OF TYPE-5 AND INTRACELLULAR RELEASE OF DNA GENOME [J].
CHARDONN.Y ;
DALES, S .
VIROLOGY, 1970, 40 (03) :462-&
[5]  
CHERESH DA, 1987, J BIOL CHEM, V262, P1434
[6]  
CHERESH DA, 1987, J BIOL CHEM, V262, P17703
[7]   ADENOVIRUS ENHANCEMENT OF TRANSFERRIN POLYLYSINE-MEDIATED GENE DELIVERY [J].
CURIEL, DT ;
AGARWAL, S ;
WAGNER, E ;
COTTEN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8850-8854
[8]   SYNTHESIS AND PROCESSING OF PRECURSOR TO MAJOR CORE PROTEIN OF ADENOVIRUS TYPE-2 [J].
EVERITT, E ;
MEADOR, SA ;
LEVINE, AS .
JOURNAL OF VIROLOGY, 1977, 21 (01) :199-214
[9]   TYROSINE UTILIZATION BY CULTURED MELANOMA-CELLS - ANALYSIS OF MELANIN BIOSYNTHESIS USING [TYROSINE-C-14 AND [THIOURACIL-C-14 [J].
FARISHIAN, RA ;
WHITTAKER, JR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1979, 198 (02) :449-461
[10]  
FITZGERALD LA, 1987, J BIOL CHEM, V262, P3936