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Low‐affinity neurotrophin receptor with targeted mutation of exon 3 is capable of mediating the death of axotomized neurons
Author(s) -
Murray Simon S,
Bartlett Perry F,
Lopes Elizabeth C,
Coulson Elizabeth J,
Greferath Una,
Cheema Surindar S
Publication year - 2003
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1046/j.1440-1681.2003.03827.x
Subject(s) - axotomy , low affinity nerve growth factor receptor , microbiology and biotechnology , programmed cell death , receptor , biology , neurotrophin , knockout mouse , neuroscience , apoptosis , biochemistry , regeneration (biology)
Summary 1. In vivo studies have shown that the low‐affinity 75 kDa neurotrophin receptor (p75NTR) is involved in axotomy‐induced cell death of sensory and motor neurons. To further examine the importance of p75NTR in mediating neuronal death in vivo , we examined the effect of axotomy in the p75NTR‐knockout mouse, which has a disrupted ligand‐binding domain. 2. The extent of sensory and motor neuron loss in the p75NTR‐knockout mouse following axotomy was not significantly different to that in wild‐type mice. This suggests that disruption of the ligand‐binding domain is insufficient to block the cell death process in axotomized neurons. 3. Immunohistochemical studies showed that axotomized neurons continue to express this mutant receptor with its intracellular death‐signalling moiety intact. 4. Treatment with antisense oligonucleotides targeted against p75NTR resulted in significant reduction in the loss of axotomized neurons in the knockout mouse. 5. These data suggest that the intracellular domain of p75NTR is essential for death‐signalling and that p75NTR can signal apoptosis, despite a disrupted ligand‐binding domain.