High basal expression and injury-induced down regulation of two regulator of G-protein signaling transcripts, RGS3 and RGS4 in primary sensory neurons

被引:18
作者
Costigan, M
Samad, TA
Allchorne, A
Lanoue, C
Tate, S
Woolf, CJ
机构
[1] Massachusetts Gen Hosp, Dept Anesthesia & Crit Care, Neural Plast Res Grp, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[3] GlaxoSmithKline Res & Dev Ltd, Mol Pharmacol, Stevenage SG1 2NY, Herts, England
关键词
D O I
10.1016/S1044-7431(03)00135-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The regulators of G-protein signaling (RGS) proteins are a family of intracellular modulators of G-protein coupled receptor (GPCR) sensitivity. They act as GTPase accelerating proteins returning the Galpha subunit back to an inactive latent state. We find that RGS3 and RGS4 are constitutively expressed at high levels in C-fiber primary sensory neurons in the adult rat dorsal root ganglion (DRG) and transection of the sciatic nerve results in a substantial down regulation of these transcripts. RGS4 mRNA is expressed only in GDNF-responsive neurons and GDNF supports the expression of this transcript in primary DRG cultures. A PDZ domain containing subtype of RGS3 is the most abundant and regulated form of this protein within the DRG. Decreased levels of RGS3 and RGS4 in injured sensory neurons is likely to result in an increased GPCR sensitivity, and therefore contribute to alterations in cellular function seen after such lesions. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:106 / 116
页数:11
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