Morphological evidence for functional capsaicin receptor expression and calcitonin gene-related peptide exocytosis in isolated peripheral nerve axons of the mouse

被引:83
作者
Bernardini, N
Neuhuber, W
Reeh, PW
Sauer, SK
机构
[1] Univ Erlangen Nurnberg, Inst Physiol & Expt Pathophysiol, D-91054 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Inst Anat, D-91054 Erlangen, Germany
关键词
capsaicin; release; calcitonin gene-related peptide; vesicular; electron microscopy; immunolocalization;
D O I
10.1016/j.neuroscience.2004.03.017
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Rat sciatic nerve axons express capsaicin, proton and heat sensitivity and respond to stimulation with a Ca2+-dependent and graded calcitonin gene-related peptide (CGRP) release. In this study we demonstrate that similar functions, including capsaicin-induced CGRP release, are to be found in the desheathed sciatic nerve of the mouse. We have morphologically investigated the mechanisms of this axonal release in regions away from the active zones of synapses. Capsaicin receptor 1 (TRPV1) and CGRP immuno-staining was performed using electron microscopic visualization. TRPV1 was identified in the axoplasm and inside vesicles-presumably on axonal transport-as well as in considerable quantity in the axonal plasma membrane of unmyelinated nerve fibers. Most of the unmyelinated axons were immunopositive for CGRP and in unstimulated nerves CGRP-containing vesicles almost entirely filled the axoplasm. After capsaicin stimulation (10(-6) M for 5 min), the fibers appeared depleted of CGRP with only few vesicles remaining as well as some residual staining of the axoplasm. In addition a large number of vesicles were fused with the axonal membrane, forming classical exocytotic figures-the omega structures-lined with CGRP immunoreactive product. These results present morphological evidence for the distribution of TRPV1 along unmyelinated axons in peripheral nerve and also provide the first demonstration of vesicular neuropeptide exocytosis along unmyelinated axons in peripheral nerve. (C) 2004 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:585 / 590
页数:6
相关论文
共 49 条
[1]
Local inflammation increases vanilloid receptor 1 expression within distinct subgroups of DRG neurons [J].
Amaya, F ;
Oh-Hashi, K ;
Naruse, Y ;
Iijima, N ;
Ueda, M ;
Shimosato, G ;
Tominaga, M ;
Tanaka, Y ;
Tanaka, M .
BRAIN RESEARCH, 2003, 963 (1-2) :190-196
[2]
Vanilloid receptor 1 expression in the rat urinary tract [J].
Avelino, A ;
Cruz, C ;
Nagy, I ;
Cruz, F .
NEUROSCIENCE, 2002, 109 (04) :787-798
[3]
BERNARDINI N, 2001, SOC NEUR ABSTR, V27
[4]
SYNTHETIC INTERSTITIAL FLUID FOR ISOLATED MAMMALIAN TISSUE [J].
BRETAG, AH .
LIFE SCIENCES PART 1 PHYSIOLOGY AND PHARMACOLOGY AND PART 2 BIOCHEMISTRY GENERAL AND MOLECULAR BIOLOGY, 1969, 8 (5P1) :319-&
[5]
Brown D A, 1981, Adv Biochem Psychopharmacol, V29, P321
[6]
The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[7]
PATHWAYS TO REGULATED EXOCYTOSIS IN NEURONS [J].
DECAMILLI, P ;
JAHN, R .
ANNUAL REVIEW OF PHYSIOLOGY, 1990, 52 :625-645
[8]
Differential effects of calcitonin gene-related peptide and calcitonin gene-related peptide 8-37 upon responses to N-methyl-D-aspartate or (R,S)-α-amino-3-hydroxy-5-methylisoxazole-4-propionate in spinal nociceptive neurons with knee joint input in the rat [J].
Ebersberger, A ;
Issa, PC ;
Vanegas, H ;
Schaible, HG .
NEUROSCIENCE, 2000, 99 (01) :171-178
[9]
The cAMP transduction cascade mediates the PGE2-induced inhibition of potassium currents in rat sensory neurones [J].
Evans, AR ;
Vasko, MR ;
Nicol, GD .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 516 (01) :163-178
[10]
ATP: an extracellular signaling molecule between neurons and glia [J].
Fields, RD ;
Stevens, B .
TRENDS IN NEUROSCIENCES, 2000, 23 (12) :625-633