2001
DOI: 10.1590/s0100-879x2001000300012
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Apoptosis of sensory neurons and satellite cells after sciatic nerve transection in C57BL/6J mice

Abstract: The rate of axonal regeneration, after sciatic nerve lesion in adult C57BL/6J mice, is reduced when compared to other isogenic strains. It was observed that such low regeneration was not due just to a delay, since neuronal death was observed. Two general mechanisms of cell death, apoptosis and necrosis, may be involved. By using the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) technique, we demonstrated that a large number of sensory neurons, as well as satellite cells found in the dors… Show more

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Cited by 19 publications
(10 citation statements)
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“…The facts reported above are in line with other works dealing with various isogenic strains of mice showing variations in the regenerative capacity after crushing or sectioning of the sciatic nerve (Lainetti et al, 1995;Lu et al, 1994;Oliveira and Langone, 2000;Oliveira, 2001;Xin et al, 1990). In this sense, C57BL/6J number of regenerated axons, 2 weeks after axotomy, was one-fifth of that in A/J.…”
Section: Introductionsupporting
confidence: 90%
“…The facts reported above are in line with other works dealing with various isogenic strains of mice showing variations in the regenerative capacity after crushing or sectioning of the sciatic nerve (Lainetti et al, 1995;Lu et al, 1994;Oliveira and Langone, 2000;Oliveira, 2001;Xin et al, 1990). In this sense, C57BL/6J number of regenerated axons, 2 weeks after axotomy, was one-fifth of that in A/J.…”
Section: Introductionsupporting
confidence: 90%
“…By cross-comparing our gene list with up-regulated genes in a model of pre-conditioned DRG32 as well as known RAGs (Supplementary Table S6), we uncover additional novel RAGs in our injury model via scRNA-seq. These novel RAG genes are connected by the known RAGs genes such as Atf3, c-Jun, Sox11 and Klf6 in regeneration gene network analysis as well4546474849.…”
Section: Discussionmentioning
confidence: 99%
“…Studies have demonstrated that this condition causes structural, electrophysiological, molecular and metabolic changes in mammalian dorsal root ganglia (DRG) cells and spinal cord. These changes include progressive loss of cells (Oliveira, 2001;Jiang and Jakobsen, 2010), proliferation and activation of satellite glial cells (Hanani, 2005) and reorganisation of the metabolic priorities of neural cells (Enes et al, 2010). There is evidence that the transection of facial and hypoglossal nerves produces a significant increase in glucose utilisation in motor nuclei of these nerves in rats (Kreutzberg and Emmert, 1980).…”
Section: Introductionmentioning
confidence: 99%