Glial cell line-derived neurotrophic factor is a survival factor for isolectin B4-positive, but not vanilloid receptor 1-positive, neurons in the mouse

被引:184
作者
Zwick, M
Davis, BM
Woodbury, CJ
Burkett, JN
Koerber, HR
Simpson, JF
Albers, KM
机构
[1] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15261 USA
[3] Univ Kentucky, Sch Med, Dept Anat & Neurobiol, Lexington, KY 40536 USA
[4] Univ Kentucky, Sch Med, Dept Pathol, Lexington, KY 40536 USA
关键词
glial cell line-derived growth factor; transgenic mice; cutaneous; sensory neuron; somatosensory; development;
D O I
10.1523/JNEUROSCI.22-10-04057.2002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Most, if not all, nociceptor sensory neurons are dependent on nerve growth factor (NGF) during early embryonic development. A large subpopulation of these sensory neurons loses NGF dependency between embryonic day 16 and postnatal day 14 and become responsive to glial cell line-derived growth factor (GDNF), a member of the transforming growth factor beta (TGF-beta) family. To examine the survival and phenotypic effects of GDNF on sensory neurons in vivo, we generated transgenic mice that overexpress GDNF in the skin. GDNF-overexpresser mice had increased numbers of small unmyelinated sensory neurons that express the tyrosine kinase receptor Ret and bind the plant isolectin B4 (IB4). Surprisingly, in wild-type and trans-genic mice, few (similar to2%) IB4-positive neurons expressed the vanilloid receptor VR1, a heat-sensitive receptor expressed by many IB4-positive neurons of the rat. Thus, in mouse, GDNF-dependent IB4-positive neurons must use a non-VR1 heat receptor. In addition, the behavior of GDNF-overexpresser animals to noxious heat or mechanical stimuli was indistinguishable from wild-type animals, indicating that, on a behavioral level, peripherally applied GDNF does not alter the sensitivity of the somatosensory system.
引用
收藏
页码:4057 / 4065
页数:9
相关论文
共 54 条
[1]   OVEREXPRESSION OF NERVE GROWTH-FACTOR IN EPIDERMIS OF TRANSGENIC MICE CAUSES HYPERTROPHY OF THE PERIPHERAL NERVOUS-SYSTEM [J].
ALBERS, KM ;
WRIGHT, DE ;
DAVIS, BM .
JOURNAL OF NEUROSCIENCE, 1994, 14 (03) :1422-1432
[2]   Cutaneous overexpression of NT-3 increases sensory and sympathetic neuron number and enhances touch dome and hair follicle innervation [J].
Albers, KM ;
Perrone, TN ;
Goodness, TP ;
Jones, ME ;
Green, MA ;
Davis, BM .
JOURNAL OF CELL BIOLOGY, 1996, 134 (02) :487-497
[3]   IMMUNOCYTOCHEMICAL LOCALIZATION OF TRKA RECEPTORS IN CHEMICALLY IDENTIFIED SUBGROUPS OF ADULT-RAT SENSORY NEURONS [J].
AVERILL, S ;
MCMAHON, SB ;
CLARY, DO ;
REICHARDT, LF ;
PRIESTLEY, JV .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1995, 7 (07) :1484-1494
[4]   TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret [J].
Baloh, RH ;
Tansey, MG ;
Golden, JP ;
Creedon, DJ ;
Heuckeroth, RO ;
Keck, CL ;
Zimonjic, DB ;
Popescu, NC ;
Johnson, EM ;
Milbrandt, J .
NEURON, 1997, 18 (05) :793-802
[5]   Artemin, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRα3-RET receptor complex [J].
Baloh, RH ;
Tansey, MG ;
Lampe, PA ;
Fahrner, TJ ;
Enomoto, H ;
Simburger, KS ;
Leitner, ML ;
Araki, T ;
Johnson, EM ;
Milbrandt, J .
NEURON, 1998, 21 (06) :1291-1302
[6]  
Bennett DLH, 1998, J NEUROSCI, V18, P3059
[7]   Potent analgesic effects of GDNF in neuropathic pain states [J].
Boucher, TJ ;
Okuse, K ;
Bennett, DLH ;
Munson, JB ;
Wood, JN ;
McMahon, SB .
SCIENCE, 2000, 290 (5489) :124-127
[8]   The expression of P2X3 purinoreceptors in sensory neurons:: Effects of axotomy and glial-derived neurotrophic factor [J].
Bradbury, EJ ;
Burnstock, G ;
McMahon, SB .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1998, 12 (4-5) :256-268
[9]  
BYRNE C, 1994, DEVELOPMENT, V120, P2369
[10]   Impaired nociception and pain sensation in mice lacking the capsaicin receptor [J].
Caterina, MJ ;
Leffler, A ;
Malmberg, AB ;
Martin, WJ ;
Trafton, J ;
Petersen-Zeitz, KR ;
Koltzenburg, M ;
Basbaum, AI ;
Julius, D .
SCIENCE, 2000, 288 (5464) :306-313