Evaluation of the electrostatic field strength at the site of exocytosis in adrenal chromaffin cells

被引:20
|
作者
Rosenheck, K [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
关键词
D O I
10.1016/S0006-3495(98)74043-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Exocytosis in secretory cells consists of release from intracellular storage granules directly into the extracellular space via fusion of the granule membrane with the plasma membrane of the cell. It is considered here as comprising two distinct processes. One is the close apposition of granule and plasma membranes. The other arises from interactions between the two membranes during the process of apposition, leading to the formation of a fusion pore. In the following it is shown for the case of the adrenal medullary chromaffin cell that the fusion pore can be ascribed to electroporation of the granule membrane, triggered by the strong electric field existing at the site of exocytosis, Based on an electric surface charge model of the cytoplasmic side of the plasma membrane, resulting from the negatively charged phosphatidylserine groups, it is found that the electrostatic field strength at the site of exocytosis reaches values on the order of 10(8) V/m at small intermembrane distances of 3 nm and lower. The field strength increases with the size of the disc-shaped plasma membrane region generating the electric field, reaching an approximate limit for a radius of 10 nm, at a surface charge density of 5.4 x 10(-2) C/m(2). According to previous experimental evaluations of threshold field strength, this field is sufficiently strong to cause membrane electroporation. This step is a precondition for the subsequent membrane fusion during the ongoing process of apposition, leading to secretion.
引用
收藏
页码:1237 / 1243
页数:7
相关论文
共 50 条
  • [41] Analysis of regulated exocytosis in adrenal chromaffin cells: insights into NSF/SNAP/SNARE function
    Burgoyne, RD
    Morgan, A
    BIOESSAYS, 1998, 20 (04) : 328 - 335
  • [42] A ROLE FOR SOLUBLE NSF ATTACHMENT PROTEINS (SNAPS) IN REGULATED EXOCYTOSIS IN ADRENAL CHROMAFFIN CELLS
    MORGAN, A
    BURGOYNE, RD
    EMBO JOURNAL, 1995, 14 (02): : 232 - 239
  • [43] Involvement of Rho GTPases in calcium-regulated exocytosis from adrenal chromaffin cells
    Gasman, S
    Chasserot-Golaz, S
    Popoff, MR
    Aunis, D
    Bader, MF
    JOURNAL OF CELL SCIENCE, 1999, 112 (24) : 4763 - 4771
  • [44] Protein Kinase C Controls the Priming Step of Regulated Exocytosis in Adrenal Chromaffin Cells
    Hiroaki Misonou
    Mica Ohara-Imaizumi
    Takeshi Murakami
    Masakazu Kawasaki
    Ken Ikeda
    Takeshi Wakai
    Konosuke Kumakura
    Cellular and Molecular Neurobiology, 1998, 18 (4) : 379 - 390
  • [45] Ca2+ Syntillas Inhibit Spontaneous Exocytosis In Mouse Adrenal Chromaffin Cells
    Lefkowitz, Jason J.
    Fogarty, Kevin E.
    Walsh, John V., Jr.
    De Crescenzo, Valerie
    BIOPHYSICAL JOURNAL, 2009, 96 (03) : 99A - 99A
  • [46] The role for Rabphilin3a in regulated exocytosis: Studies in adrenal chromaffin cells.
    Chung, SH
    Macara, IG
    Stabila, P
    Holz, RW
    MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 2594 - 2594
  • [47] Mitochondria regulate the Ca2+-exocytosis relationship of bovine adrenal chromaffin cells
    Giovannucci, DR
    Hlubek, MD
    Stuenkel, EL
    JOURNAL OF NEUROSCIENCE, 1999, 19 (21): : 9261 - 9270
  • [48] EFFECTS OF TETANUS TOXIN AND BOTULINUM A TOXIN ON EXOCYTOSIS FROM PERMEABILIZED ADRENAL CHROMAFFIN CELLS
    AHNERTHILGER, G
    STECHER, B
    GRATZL, M
    BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1989, 370 (07): : 613 - 613
  • [49] LOSS OF PROTEINS FROM DIGITONIN-PERMEABILIZED ADRENAL CHROMAFFIN CELLS ESSENTIAL FOR EXOCYTOSIS
    SARAFIAN, T
    AUNIS, D
    BADER, MF
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1987, 262 (34) : 16671 - 16676
  • [50] PARDAXIN INDUCES EXOCYTOSIS IN BOVINE ADRENAL-MEDULLARY CHROMAFFIN CELLS INDEPENDENT OF CALCIUM
    LAZAROVICI, P
    LELKES, PI
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1992, 263 (03): : 1317 - 1326