ATP-independent luminal oscillations and release of Ca2+ and H+ from mast cell secretory granules:: Implications for signal transduction

被引:36
作者
Quesada, I
Chin, WC
Verdugo, P
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[2] Univ Washington, Friday Harbor Labs, Seattle, WA 98195 USA
[3] FAMU FSU, Dept Chem Engn, Tallahassee, FL 32310 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(03)74535-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
InsP(3) is an important link in the intracellular information network. Previous observations show that activation of InsP(3)-receptor channels on the granular membrane can turn secretory granules into Ca2+ oscillators that deliver periodic trains of Ca2+ release to the cytosol (T. Nguyen, W. C. Chin, and P. Verdugo, 1998, Nature, 395: 908-912; I. Quesada, W. C. Chin, J. Steed, P. Campos-Bedolla, and P. Verdugo, 2001, Biophys. J. 80: 2133-2139). Here we show that InsP(3) can also turn mast cell granules into proton oscillators. InsP(3)-induced intralumenal [H+] oscillations are ATP-independent, result from H+/K+ exchange in the heparin matrix, and produce perigranular pH oscillations with the same frequency. These perigranular pH oscillations are in-phase with intralumenal [H+] but out-of-phase with the corresponding perigranular [Ca2+] oscillations. The low pH of the secretory compartment has critical implications in a broad range of intracellular processes. However, the association of proton release with InsP(3)-induced Ca2+ signals, their similar periodic nature, and the sensitivity of important exocytic proteins to the joint action of Ca2+ and pH strongly suggests that granules might encode a combined Ca2+/H+ intracellular signal. A H+/Ca2+ signal could significantly increase the specificity of the information sent by the granule by transmitting two frequency encoded messages targeted exclusively to proteins like calmodulin, annexins, or syncollin that are crucial for exocytosis and require specific combinations of [Ca2+] "and'' pH for their action.
引用
收藏
页码:963 / 970
页数:8
相关论文
共 51 条
[21]   Modulation of N-type Ca2+ channels by intracellular pH in chick sensory neurons [J].
Kiss, L ;
Korn, SJ .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 81 (04) :1839-1847
[22]   The annexin II-p11 complex is involved in regulated exocytosis in bovine pulmonary artery endothelial cells [J].
König, J ;
Prenen, J ;
Nilius, B ;
Gerke, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (31) :19679-19684
[23]   A transmembrane form of annexin XII detected by site-directed spin labeling [J].
Langen, R ;
Isas, JM ;
Hubbell, WL ;
Haigler, HT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14060-14065
[24]   Kinetics of release of serotonin from isolated secretory granules .2. Ion exchange determines the diffusivity of serotonin [J].
Marszalek, PE ;
Farrell, B ;
Verdugo, P ;
Fernandez, JM .
BIOPHYSICAL JOURNAL, 1997, 73 (03) :1169-1183
[25]   Dense core secretory vesicles revealed as a dynamic Ca2+ store in neuroendocrine cells with a vesicle-associated membrane protein aequorin chimaera [J].
Mitchell, KJ ;
Pinton, P ;
Varadi, A ;
Tacchetti, C ;
Ainscow, EK ;
Pozzan, T ;
Rizzuto, R ;
Rutter, GA .
JOURNAL OF CELL BIOLOGY, 2001, 155 (01) :41-51
[26]   THIN-SECTION RATIOMETRIC CA2+ IMAGES OBTAINED BY OPTICAL SECTIONING OF FURA-2 LOADED MAST-CELLS [J].
MONCK, JR ;
OBERHAUSER, AF ;
KEATING, TJ ;
FERNANDEZ, JM .
JOURNAL OF CELL BIOLOGY, 1992, 116 (03) :745-759
[27]   Vesicular Ca2+ participates in the catalysis of exocytosis [J].
Mundorf, ML ;
Troyer, KP ;
Hochstetler, SE ;
Near, JA ;
Wightman, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) :9136-9142
[28]   THE SECRETORY GRANULE MATRIX - A FAST-ACTING SMART POLYMER [J].
NANAVATI, C ;
FERNANDEZ, JM .
SCIENCE, 1993, 259 (5097) :963-965
[29]   Role of Ca2+/K+ ion exchange in intracellular storage and release of Ca2+ [J].
Nguyen, T ;
Chin, WC ;
Verdugo, P .
NATURE, 1998, 395 (6705) :908-912
[30]   Protein kinase C as a molecular machine for decoding calcium and diacylglycerol signals [J].
Oancea, E ;
Meyer, T .
CELL, 1998, 95 (03) :307-318