Gene targeting reveals a critical role for neurturin in the development and maintenance of enteric, sensory, and parasympathetic neurons

被引:260
作者
Heuckeroth, RO
Enomoto, H
Grider, JR
Golden, JP
Hanke, JA
Jackman, A
Molliver, DC
Bardgett, ME
Snider, WD
Johnson, EM
Milbrandt, J [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[7] Virginia Commonwealth Univ, Med Coll Virginia, Dept Physiol, Richmond, VA 23298 USA
[8] Virginia Commonwealth Univ, Med Coll Virginia, Dept Med, Richmond, VA 23298 USA
关键词
D O I
10.1016/S0896-6273(00)81087-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurturin (NTN) is a neuronal survival factor that activates the Ret tyrosine kinase in the presence of a GPI-linked coreceptor (either GFR alpha 1 or GFR alpha 2). Neurturin-deficient (NTN-/-) mice generated by homologous recombination are viable and fertile but have defects in the enteric nervous system, including reduced myenteric plexus innervation density and reduced gastrointestinal motility. Parasympathetic innervation of the lacrimal and submandibular salivary gland is dramatically reduced in NTN-/- mice, indicating that Neurturin is a neurotrophic factor for parasympathetic neurons, GFR alpha 2-expressing cells in the trigeminal and dorsal root ganglia are also depleted in NTN-/- mice. The loss of GFR alpha 2-expressing neurons, in conjunction with earlier studies, provides strong support for GFR alpha 2/Ret receptor complexes as the critical mediators of NTN function in vivo.
引用
收藏
页码:253 / 263
页数:11
相关论文
共 57 条
[1]   PREDOMINANT SYMPTOMS IN IRRITABLE-BOWEL-SYNDROME CORRELATE WITH SPECIFIC AUTONOMIC NERVOUS-SYSTEM ABNORMALITIES [J].
AGGARWAL, A ;
CUTTS, TF ;
ABELL, TL ;
CARDOSO, S ;
FAMILONI, B ;
BREMER, J ;
KARAS, J .
GASTROENTEROLOGY, 1994, 106 (04) :945-950
[2]   ACUTE ANOSMIA IN RAT - BEHAVIORAL TEST OF A PERIPHERALLY-INDUCED OLFACTORY DEFICIT [J].
ALBERTS, JR ;
GALEF, BG .
PHYSIOLOGY & BEHAVIOR, 1971, 6 (05) :619-&
[3]   GFRα3 is an orphan member of the GDNF/neurturin/persephin receptor family [J].
Baloh, RH ;
Gorodinsky, A ;
Golden, JP ;
Tansey, MG ;
Keck, CL ;
Popescu, NC ;
Johnson, EM ;
Milbrandt, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (10) :5801-5806
[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]   Kainic acid lesions enhance locomotor responses to novelty, saline, amphetamine, and MK-801 [J].
Bardgett, ME ;
Jacobs, PS ;
Jackson, JL ;
Csernansky, JG .
BEHAVIOURAL BRAIN RESEARCH, 1997, 84 (1-2) :47-55
[7]   The effects of kainic acid lesions on locomotor responses to haloperidol and clozapine [J].
Bardgett, ME ;
Jackson, JL ;
Taylor, BM ;
Csernansky, JG .
PSYCHOPHARMACOLOGY, 1998, 135 (03) :270-278
[8]  
Bennett DLH, 1998, J NEUROSCI, V18, P3059
[9]   GDNF IS AN AGE-SPECIFIC SURVIVAL FACTOR FOR SENSORY AND AUTONOMIC NEURONS [J].
BUJBELLO, A ;
BUCHMAN, VL ;
HORTON, A ;
ROSENTHAL, A ;
DAVIES, AM .
NEURON, 1995, 15 (04) :821-828
[10]   Neurturin responsiveness requires a GPI-linked receptor and the Ret receptor tyrosine kinase [J].
BujBello, A ;
Adu, J ;
Pinon, LGP ;
Horton, A ;
Thompson, J ;
Rosenthal, A ;
Chinchetru, M ;
Buchman, VL ;
Davies, AM .
NATURE, 1997, 387 (6634) :721-724