Nerve injury induces glial cell line-derived neurotrophic factor (gdnf) expression in schwann cells through purinergic signaling and the pkc-pkd pathway

被引:61
作者
Xu, Pin [1 ,2 ]
Rosen, Kenneth M. [1 ,3 ]
Hedstrom, Kristian [1 ,2 ]
Rey, Osvaldo [4 ,5 ]
Guha, Sushovan [6 ,7 ]
Hart, Courtney [1 ]
Corfas, Gabriel [1 ,2 ,3 ]
机构
[1] Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Otolaryngol, Boston, MA 02115 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Unit Signal Transduct & Gastrointestinal Canc, Div Digest Dis,Dept Med, Los Angeles, CA 90095 USA
[5] UBA, CONICET, INIGEM, Buenos Aires, DF, Argentina
[6] UT Hlth UT Hlth Sci Ctr, Div Gastroenterol Hepatol & Nutr, Houston, TX USA
[7] Med Sch Houston, Houston, TX USA
基金
美国国家卫生研究院;
关键词
GDNF; purinergic receptor; nerve injury; protein kinase D; apyrase; Schwann cell; PROTEIN-KINASE-D; DORSAL-ROOT GANGLIA; PERIPHERAL-NERVE; SPINAL-CORD; DIFFERENTIAL REGULATION; SENSORY NEURONS; IN-VIVO; AXONAL REGENERATION; DYNAMIC REGULATION; FAMILY RECEPTORS;
D O I
10.1002/glia.22491
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Upon peripheral nerve injury, specific molecular events, including increases in the expression of selected neurotrophic factors, are initiated to prepare the tissue for regeneration. However, the mechanisms underlying these events and the nature of the cells involved are poorly understood. We used the injury-induced upregulation of glial cell-derived neurotrophic factor (GDNF) expression as a tool to gain insights into these processes. We found that both myelinating and nonmyelinating Schwann cells are responsible for the dramatic increase in GDNF expression after injury. We also demonstrate that the GDNF upregulation is mediated by a signaling cascade involving activation of Schwann cell purinergic receptors, followed by protein kinase C signaling which activates protein kinase D (PKD), which leads to increased GDNF transcription. Given the potent effects of GDNF on survival and repair of injured peripheral neurons, we propose that targeting these pathways may yield therapeutic tools to treat peripheral nerve injury and neuropathies.
引用
收藏
页码:1029 / 1040
页数:12
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