Distribution of calcitonin gene-related peptide at the neuromuscular junction of mdx mice

被引:2
作者
Marques, MJ [1 ]
Minatel, E [1 ]
Guimaraes, AO [1 ]
Santo Neto, H [1 ]
机构
[1] Univ Estadual Campinas, Dept Anat, Inst Biol, BR-13083970 Campinas, SP, Brazil
来源
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY | 2004年 / 279A卷 / 02期
关键词
acetylcholine receptor; calcitonin gene-related peptide; confocal microscopy; neuromuscular junction; mdx mice;
D O I
10.1002/ar.a.20068
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
In normal skeletal muscle, the protein dystrophin is associated with plasma membrane glycoproteins and may be involved in the stabilization of the sarcolemma. Mutant mdx mice are markedly deficient in dystrophin and show muscle fiber necrosis followed by regeneration. Changes in the distribution of acetylcholine receptors (AChRs) have been reported at the neuromuscular junction of mdx mice possibly as a result of alterations in the release or response to neural trophic factors. One such factor is calcitonin gene-related peptide (CGRP), which has been implicated in AChR synthesis and function. In this study, we used rhodamine-a-bungarotoxin and anti-CGRP IgG FITC to study AChR and CGRP distribution at the neuromuscular junction of mdx mice. Using laser scanning fluorescence confocal microscopy, it was possible to see that CGRP-like immunoreactivity had a presynaptic distribution, covering the AChRs. Thirty-four percent of dystrophic junctions were found to be labeled with CGRP compared to 80% of control endplates. Since CGRP-positive and -negative fibers showed similar changes in AChR distribution, it is suggested that CGRP is probably not directly involved in the altered pattern of AChR seen in dystrophin-deficient muscle fibers of mdx mice. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:798 / 803
页数:6
相关论文
共 32 条
[11]   ARIA IS CONCENTRATED IN THE SYNAPTIC BASAL LAMINA OF THE DEVELOPING CHICK NEUROMUSCULAR-JUNCTION [J].
GOODEARL, ADJ ;
YEE, AG ;
SANDROCK, AW ;
CORFAS, G ;
FISCHBACH, GD .
JOURNAL OF CELL BIOLOGY, 1995, 130 (06) :1423-1434
[12]   DYSTROPHIN - THE PROTEIN PRODUCT OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS [J].
HOFFMAN, EP ;
BROWN, RH ;
KUNKEL, LM .
CELL, 1987, 51 (06) :919-928
[14]   ARIA CAN BE RELEASED FROM EXTRACELLULAR-MATRIX THROUGH CLEAVAGE OF A HEPARIN-BINDING DOMAIN [J].
LOEB, JA ;
FISCHBACH, GD .
JOURNAL OF CELL BIOLOGY, 1995, 130 (01) :127-135
[15]   Mice lacking α-calcitonin gene-related peptide exhibit normal cardiovascular regulation and neuromuscular development [J].
Lu, JT ;
Son, YJ ;
Lee, J ;
Jetton, TL ;
Shiota, M ;
Moscoso, L ;
Niswender, KD ;
Loewy, AD ;
Magnuson, MA ;
Sanes, JR ;
Emeson, RB .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1999, 14 (02) :99-120
[16]   STRUCTURE AND FUNCTION OF THE NEUROMUSCULAR-JUNCTION IN YOUNG-ADULT MDX MICE [J].
LYONS, PR ;
SLATER, CR .
JOURNAL OF NEUROCYTOLOGY, 1991, 20 (12) :969-981
[17]   Acetylcholine receptors and nerve terminal distribution at the neuromuscular junction of non-obese diabetic mice [J].
Marques, MJ ;
Neto, HS .
ANATOMICAL RECORD, 2002, 267 (02) :112-119
[18]   Imaging neuromuscular junctions by confocal fluorescence microscopy: individual endplates seen in whole muscles with vital intracellular staining of the nerve terminals [J].
Marques, MJ ;
Santo Neto, H .
JOURNAL OF ANATOMY, 1998, 192 :425-430
[19]   From plaque to pretzel: Fold formation and acetylcholine receptor loss at the developing neuromuscular junction [J].
Marques, MJ ;
Conchello, JA ;
Lichtman, JW .
JOURNAL OF NEUROSCIENCE, 2000, 20 (10) :3663-3675
[20]   DIFFERENTIAL EFFECT OF ALPHA-LATROTOXIN ON EXOCYTOSIS FROM SMALL SYNAPTIC VESICLES AND FROM LARGE DENSE-CORE VESICLES CONTAINING CALCITONIN GENE-RELATED PEPTIDE AT THE FROG NEUROMUSCULAR-JUNCTION [J].
MATTEOLI, M ;
HAIMANN, C ;
TORRITARELLI, F ;
POLAK, JM ;
CECCARELLI, B ;
DECAMILLI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7366-7370