STRUCTURE, FUNCTION, AND REGULATION OF CELLULAR TIGHT JUNCTIONS

被引:412
作者
SCHNEEBERGER, EE [1 ]
LYNCH, RD [1 ]
机构
[1] UNIV MASSACHUSETTS, DEPT BIOL SCI, LOWELL, MA 01854 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 262卷 / 06期
关键词
ZONULA-OCCLUDENS; JUNCTIONAL COMPLEX; CALCIUM; PERMEABILITY;
D O I
10.1152/ajplung.1992.262.6.L647
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The tight junction (TJ) is a dynamic structure that is controlled, in part, by the activity of the cytoskeleton. It has become abundantly clear that, in the presence of Ca2+, assembly of the TJ is the result of cellular interactions that trigger a complex cascade of biochemical events that ultimately lead to the formation of an organized network of TJ elements, the composition of which remains unknown. The TJ functions both as a barrier between two fluid compartments and, to a lesser extent, as a fence between apical and basolateral membrane domains. To meet the many physiological and pathological challenges to which epithelia and endothelia are subjected, the TJ must be capable of a rapid and coordinated response, which depends on complex regulatory mechanisms. The precise characterization of the mechanisms involved in the assembly and regulation of the TJ is an area of current active investigation. However, until the biochemical composition of this structure has been defined and its gene identified, the TJ will continue to be an elusive yet tantalizing challenge to the cell biologist.
引用
收藏
页码:L647 / L661
页数:15
相关论文
共 145 条
[1]  
ADELBA SM, 1991, AM J RESPIR CELL MOL, V4, P195
[2]  
ADELBA SM, 1991, J CELL BIOL, V114, P1059
[3]   CHARACTERIZATION OF ZO-1, A PROTEIN-COMPONENT OF THE TIGHT JUNCTION FROM MOUSE-LIVER AND MADIN-DARBY CANINE KIDNEY-CELLS [J].
ANDERSON, JM ;
STEVENSON, BR ;
JESAITIS, LA ;
GOODENOUGH, DA ;
MOOSEKER, MS .
JOURNAL OF CELL BIOLOGY, 1988, 106 (04) :1141-1149
[4]   DEVELOPMENT OF CELL-SURFACE POLARITY IN THE EPITHELIAL MADIN-DARBY CANINE KIDNEY (MDCK) CELL-LINE [J].
BALCAROVASTANDER, J ;
PFEIFFER, SE ;
FULLER, SD ;
SIMONS, K .
EMBO JOURNAL, 1984, 3 (11) :2687-2694
[5]   ASSEMBLY AND SEALING OF TIGHT JUNCTIONS - POSSIBLE PARTICIPATION OF G-PROTEINS, PHOSPHOLIPASE-C, PROTEIN-KINASE-C AND CALMODULIN [J].
BALDA, MS ;
GONZALEZMARISCAL, L ;
CONTRERAS, RG ;
MACIASSILVA, M ;
TORRESMARQUEZ, ME ;
SAINZ, JAG ;
CEREIJIDO, M .
JOURNAL OF MEMBRANE BIOLOGY, 1991, 122 (03) :193-202
[6]   PROTAMINE ALTERS STRUCTURE AND CONDUCTANCE OF NECTURUS GALLBLADDER TIGHT JUNCTIONS WITHOUT MAJOR ELECTRICAL EFFECTS ON THE APICAL CELL-MEMBRANE [J].
BENTZEL, CJ ;
FROMM, M ;
PALANT, CE ;
HEGEL, U .
JOURNAL OF MEMBRANE BIOLOGY, 1987, 95 (01) :9-20
[7]   HYDROPHILIC SOLUTE TRANSPORT ACROSS RAT ALVEOLAR EPITHELIUM [J].
BERG, MM ;
KIM, KJ ;
LUBMAN, RL ;
CRANDALL, ED .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (05) :2320-2327
[8]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1989, 341 (6239) :197-205
[9]   EVIDENCE THAT A GUANINE NUCLEOTIDE-BINDING PROTEIN LINKED TO A MUSCARINIC RECEPTOR INHIBITS DIRECTLY PHOSPHOLIPASE-C [J].
BIZZARRI, C ;
DIGIROLAMO, M ;
DORAZIO, MC ;
CORDA, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4889-4893
[10]  
BJORK J, 1985, J IMMUNOL, V134, P1115