Some lumbar sympathetic neurons develop a glutamatergic phenotype after peripheral axotomy with a note on VGLUT2-positive perineuronal baskets

被引:18
作者
Brumovsky, Pablo R. [1 ,2 ]
Seroogy, Kim B. [3 ]
Lundgren, Kerstin H. [3 ]
Watanabe, Masahiko [4 ]
Hokfelt, Tomas [5 ]
Gebhart, G. F. [1 ]
机构
[1] Univ Pittsburgh, Pittsburgh Ctr Pain Res, Pittsburgh, PA 15213 USA
[2] Austral Univ, Fac Biomed Sci, Buenos Aires, DF, Argentina
[3] Univ Cincinnati, Dept Neurol, Cincinnati, OH 45267 USA
[4] Hokkaido Univ, Sch Med, Dept Anat, Sapporo, Hokkaido 060, Japan
[5] Karolinska Inst, Dept Neurosci, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Autonomic neurons; Axotomy; Glutamate; Neuropeptides; Pain; Pelvic nerve; Sensory neurons; Vesicular glutamate transporter; DORSAL-ROOT GANGLIA; SUPERIOR CERVICAL-GANGLION; RAT GLABROUS SKIN; VASOACTIVE-INTESTINAL-PEPTIDE; HYDROXYLASE MESSENGER-RNA; PELVIC AUTONOMIC GANGLIA; ADULT-MOUSE BRAIN; SPINAL-CORD; NERVE INJURY; GUINEA-PIG;
D O I
10.1016/j.expneurol.2011.05.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glutamate is the main excitatory neurotransmitter in the nervous system, including in primary afferent neurons. However, to date a glutamatergic phenotype of autonomic neurons has not been described. Therefore, we explored the expression of vesicular glutamate transporter (VGLUT) types 1,2 and 3 in lumbar sympathetic chain (LSC) and major pelvic ganglion (MPG) of naive BALB/C mice, as well as after pelvic nerve axotomy (PNA), using immunohistochemistry and in situ hybridization. Colocalization with activating transcription factor-3 (ATF-3), tyrosine hydroxylase (TH), vesicular acetylcholine transporter (VAChT) and calcitonin gene-related peptide was also examined. Sham-PNA, sciatic nerve axotomy (SNA) or naive mice were included. In naive mice, VGLUT(2)-like immunoreactivity (LI) was only detected in fibers and varicosities in LSC and MPG; no ATF-3-immunoreactive (IR) neurons were visible. In contrast, PNA induced upregulation of VGLUT(2) protein and transcript, as well as of ATF-3-LI in subpopulations of LSC neurons. Interestingly, VGLUT(2)-IR LSC neurons coexpressed ATF-3, and often lacked the noradrenergic marker TH. SNA only increased VGLUT(2) protein and transcript in scattered LSC neurons. Neither PNA nor SNA upregulated VGLUT(2) in MPG neurons. We also found perineuronal baskets immunoreactive either for VGLUT(2) or the acetylcholinergic marker VAChT in non-PNA MPGs, usually around TH-IR neurons. VGLUT(1)-LI was restricted to some varicosities in MPGs, was absent in LSCs, and remained largely unaffected by PNA or SNA. This was confirmed by the lack of expression of VGLUT(1) or VGLUT(3) mRNAs in LSCs, even after PNA or SNA. Taken together, axotomy of visceral and non-visceral nerves results in a glutamatergic phenotype of some LSC neurons. In addition, we show previously non-described MPG perineuronal glutamatergic baskets. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:258 / 272
页数:15
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