FUSION PARTNERS FOR NIH 3T3 HAB2 FIBROBLASTS EXPRESSING HEMAGGLUTININ

被引:0
|
作者
FROLOV, VA
BYCHENKO, AB
DUNINABARKOVSKYA, AY
CHIZMADZHEV, YA
ZIMMERBERG, J
机构
[1] RUSSIAN ACAD MED SCI,DI IVANOVSKII VIROL INST,MOSCOW,RUSSIA
[2] MOSCOW MV LOMONOSOV STATE UNIV,AN BELOZERSKY INST PHYSICOCHEM BIOL,MOSCOW,RUSSIA
[3] NIH,BETHESDA,MD 20892
来源
BIOLOGICHESKIE MEMBRANY | 1995年 / 12卷 / 03期
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In an attempt to work out an experimental system for studying the mechanisms of fusion induced by influenza-virus fusion protein hemagglutinin (HA), several cell lines (PLC/PRF/5, BHK-21, MDCK, VERO) were tested for their ability to fuse with NIH 3T3 HA2b cells that constitutively express HA. Using fluorescent microscopy to follow the dye spread from the labelled cells to the unlabelled ones under conditions that were to activate HA (proteolytic cleavage of inactive MA) and to trigger fusion (pH drop), we have shown that only PLC PRF and BHK-21 cells fused with HA2b cells at a rate comparable with that obtained for RBC. New fusion systems, BHK/HA2b and PLC/HA2b, provide important advantages for further investigations of fusion mechanisms at a single-cell level, as both partners are easily and equally accessible for the manipulations required for high-resolution whole-cell patch-clamp measurements. PLC/HA2b system seems to be more promissing because of clear morphological differences between the partners. The mechanism of fusion tolerance displayed by other cells remians to be explained.
引用
收藏
页码:288 / 293
页数:6
相关论文
共 50 条
  • [1] CYTOSKELETAL REORGANIZATION IN NIH 3T3 FIBROBLASTS EXPRESSING THE RAS ONCOGENE
    DARTSCH, PC
    RITTER, M
    HAUSSINGER, D
    LANG, F
    EUROPEAN JOURNAL OF CELL BIOLOGY, 1994, 63 (02) : 316 - 325
  • [2] Hemagglutinin-induced fusion of HAb2 and PLC cells: Dynamics of the fusion pore conductance
    Dunina-Barkovskaya, AY
    Samsonov, AV
    Pivovarov, VS
    Frolov, VA
    BIOLOGICHESKIE MEMBRANY, 1999, 16 (04): : 461 - 471
  • [3] Characterization of AT2 receptor expression in NIH 3T3 fibroblasts
    Heemskerk, FMJ
    Zorad, S
    Xu, NZ
    Gutkind, SJ
    Saavedra, JM
    CELLULAR AND MOLECULAR NEUROBIOLOGY, 1999, 19 (02) : 277 - 288
  • [4] Characterization of AT2 Receptor Expression in NIH 3T3 Fibroblasts
    Frank M. J. Heemskerk
    Stefan Zorad
    Ningzhi Xu
    Silvio J. Gutkind
    Juan M. Saavedra
    Cellular and Molecular Neurobiology, 1999, 19 : 277 - 288
  • [5] EWS/ETS fusion genes induce epithelial and neuroectodermal differentiation in NIH 3T3 fibroblasts
    Teitell, MA
    Thompson, AD
    Sorensen, PHB
    Shimada, H
    Triche, TJ
    Denny, CT
    LABORATORY INVESTIGATION, 1999, 79 (12) : 1535 - 1543
  • [6] Cell shrinkage as a signal to apoptosis in NIH 3T3 fibroblasts
    Friis, MB
    Friborg, CR
    Schneider, L
    Nielsen, MB
    Lambert, IH
    Christensen, ST
    Hoffmann, EK
    JOURNAL OF PHYSIOLOGY-LONDON, 2005, 567 (02): : 427 - 443
  • [7] NIH 3T3 cells or engineered NIH 3T3 cells stably expressing GDNF can protect primary dopaminergic neurons
    Ma, DD
    Wang, XM
    Han, JS
    NEUROLOGICAL RESEARCH, 2000, 22 (06) : 538 - 544
  • [8] EFFECTS OF BRADYKININ ON CELL-VOLUME AND INTRACELLULAR PH IN NIH 3T3 FIBROBLASTS EXPRESSING THE RAS ONCOGENE
    RITTER, M
    WOLL, E
    HAUSSINGER, D
    LANG, F
    FEBS LETTERS, 1992, 307 (03) : 367 - 370
  • [9] EFFECTS OF CALCIUM-CHANNEL BLOCKERS ON NIH 3T3 FIBROBLASTS EXPRESSING THE HA-RAS ONCOGENE
    DARTSCH, PC
    RITTER, M
    GSCHWENTNER, M
    LANG, HJ
    LANG, F
    EUROPEAN JOURNAL OF CELL BIOLOGY, 1995, 67 (04) : 372 - 378
  • [10] Cancerous Phenotypes Exhibited by NIH/3T3 Fibroblasts Overexpressing BST-2
    Alvarez, Folnetti
    Okeoma, Chioma
    FASEB JOURNAL, 2020, 34