Literature DB >> 1769343

The effect of age on motor neurone death following axotomy in the mouse.

M M Pollin1, S McHanwell, C R Slater.   

Abstract

The ability of mouse motor neurones to survive axotomy during the first month of life was studied. The motor neurones that lie in the dorsolateral columns of spinal segments C7 and C8 and supply the flexor muscles of the forepaw were axotomized by cutting and removing part of the median and ulnar nerves above the elbow. The number and position of cell bodies with axons in these nerves were confirmed by retrograde labelling of the cut axons with horseradish peroxidase. The ability of these neurones to survive axotomy varies with the age of the animal at the time of axotomy. When the axons are sectioned within the first four postnatal days, 80-90% of the cell bodies will die, more than half of this death occurring in less than one week after axotomy. If the animals are one week old at the time the nerves are cut, a significantly smaller number (50%) die (P = 0.013), and the time-course of death is different, with eight to ten days elapsing before half the death has occurred. 40% of the neurones will die if sectioned at two weeks of age, and it is not until four weeks of age that more than 90% of the cells can survive axotomy. We conclude, therefore, that the kinetics of motor neurone death, as well as the final extent of neuronal loss, are affected by the age at which the animal is axotomized.

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Year:  1991        PMID: 1769343     DOI: 10.1242/dev.112.1.83

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  12 in total

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8.  A serine protease inhibitor, protease nexin I, rescues motoneurons from naturally occurring and axotomy-induced cell death.

Authors:  L J Houenou; P L Turner; L Li; R W Oppenheim; B W Festoff
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9.  Axotomized neonatal motoneurons overexpressing the bcl2 proto-oncogene retain functional electrophysiological properties.

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10.  Rescue of adult mouse motoneurons from injury-induced cell death by glial cell line-derived neurotrophic factor.

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