Ultrastructural localization of brain-derived neurotrophic factor in rat primary sensory neurons

被引:62
作者
Luo, XG
Rush, RA
Zhou, XF
机构
[1] Flinders Univ S Australia, Dept Human Physiol, Adelaide, SA 5001, Australia
[2] Human Med Univ, Dept Anat, Changsha, Hunan, Peoples R China
[3] Flinders Univ S Australia, Ctr Neurosci, Adelaide, SA 5001, Australia
关键词
mitochondria; vesicles; spinal cord; calcitonin gene related peptide; p75 low affinity neurotrophin receptor;
D O I
10.1016/S0168-0102(00)00238-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In a previous study we have shown that brain-derived neurotrophic factor (BDNF) is present in a subpopulation of small- to medium-sized sensory neurons in the dorsal root ganglia (DRG) and is anterogradely transported in both the peripheral and central processes. Within the spinal cord, BDNF is localized to varicosities of sensory nerve terminals in laminae I and II of the dorsal horn. This study raised the question of whether BDNF is localized in synaptic vesicles of the afferent nerve terminals. Using immunohistochemical and immunocytochemical techniques we have now investigated the ultrastructural localization of BDNF in the spinal cord of the rat. In addition, its colocalization with the low affinity neurotrophin receptor, p75, and calcitonin gene related peptide (CGRP) was also investigated. In lamina II of the spinal cord, BDNF immunoreactivity was restricted to nerve terminals. The reaction product appeared associated with dense-cored and clear vesicles of terminals superficial laminae. Double labelling experiments at the light microscopic level showed that 55% of BDNF immunoreactive neurons in DRG are colocalized with CGRP and many nerve terminals in laminae I and II of the spinal cord contained both BDNF and CGRP immunoreactivities. The results of double labelling at the ultrastructural level showed that most BDNF-ir (immunoreactive) nerve terminals contained CGRP or the low affinity neurotrophin receptor, p75, but nut vice versa. These results point to the conclusion that BDNF may be released in parallel with neurotransmitters from nerve terminals in the: spinal cord from a subpopulation of nociceptive primary afferents. (C) 2001 Elsevier Science Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:377 / 384
页数:8
相关论文
共 34 条
[1]   A BDNF AUTOCRINE LOOP IN ADULT SENSORY NEURONS PREVENTS CELL DEATH [J].
ACHESON, A ;
CONOVER, JC ;
FANDL, JP ;
DECHIARA, TM ;
RUSSELL, M ;
THADANI, A ;
SQUINTO, SP ;
YANCOPOULOS, GD ;
LINDSAY, RM .
NATURE, 1995, 374 (6521) :450-453
[2]   Non target-derived roles of the neurotrophins [J].
Acheson, A ;
Lindsay, RM .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1996, 351 (1338) :417-422
[3]   Fast actions of neurotrophic factors [J].
Berninger, B ;
Poo, MM .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (03) :324-330
[4]  
BUCHMAN VL, 1993, DEVELOPMENT, V118, P989
[5]   NEUROTROPHIN RECEPTORS - A WINDOW INTO NEURONAL DIFFERENTIATION [J].
CHAO, MV .
NEURON, 1992, 9 (04) :583-593
[6]   DIFFERENTIAL ROLE OF THE LOW-AFFINITY NEUROTROPHIN RECEPTOR (P75) IN RETROGRADE AXONAL-TRANSPORT OF THE NEUROTROPHINS [J].
CURTIS, R ;
ADRYAN, KM ;
STARK, JL ;
PARK, JS ;
COMPTON, DL ;
WESKAMP, G ;
HUBER, LJ ;
CHAO, MV ;
JAENISCH, R ;
LEE, KF ;
LINDSAY, RM ;
DISTEFANO, PS .
NEURON, 1995, 14 (06) :1201-1211
[7]   MICE LACKING BRAIN-DERIVED NEUROTROPHIC FACTOR DEVELOP WITH SENSORY DEFICITS [J].
ERNFORS, P ;
LEE, KF ;
JAENISCH, R .
NATURE, 1994, 368 (6467) :147-150
[8]   IDENTIFICATION OF CELLS IN RAT-BRAIN AND PERIPHERAL-TISSUES EXPRESSING MESSENGER-RNA FOR MEMBERS OF THE NERVE GROWTH-FACTOR FAMILY [J].
ERNFORS, P ;
WETMORE, C ;
OLSON, L ;
PERSSON, H .
NEURON, 1990, 5 (04) :511-526
[9]   Regulation of synaptic responses to high-frequency stimulation and LTP by neurotrophins in the hippocampus [J].
Figurov, A ;
PozzoMiller, LD ;
Olafsson, P ;
Wang, T ;
Lu, B .
NATURE, 1996, 381 (6584) :706-709
[10]  
GIBBINS IL, 1987, CELL TISSUE RES, V248, P417