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Claudin-15 overexpression inhibits proliferation and promotes apoptosis of Schwann cells in vitro 被引量:1

Claudin-15 overexpression inhibits proliferation and promotes apoptosis of Schwann cells in vitro
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摘要 Our previous experiments have discovered that Claudin-15 was up-regulated in Schwann cells of the distal nerve stumps of rat models of sciatic nerve injury.However,how Claudin-15 affects Schwann cell function is still unknown.This study aimed to identify the effects of Claudin-15 on proliferation and apoptosis of Schwann cells cultured in vitro and explore the underlying mechanisms.Primary Schwann cells were obtained from rats.Claudin-15 in Schwann cells was knocked down using siRNA(siRNA-1 group)compared with the negative control siRNA transfection group(negative control group).Claudin-15 in Schwann cells was overexpressed using pGV230-Claudin-15 plasmid(pGV230-Claudin-15 group).The pGV230 transfection group(pGV230 group)acted as the control of the pGV230-Claudin-15 group.Cell proliferation was analyzed with EdU assay.Cell apoptosis was analyzed with flow cytometric analysis.Cell migration was analyzed with Transwell inserts.The mRNA and protein expressions were analyzed with quantitative polymerase chain reaction assay and western blot assay.The results showed that compared with the negative control group,cell proliferation rate was up-regulated;p-AKT/AKT ratio,apoptotic rate,p-c-Jun/c-Jun ratio,mRNA expression of protein kinase C alpha,Bcl-2 and Bax were down-regulated;and mRNA expression of neurotrophins basic fibroblast growth factor and neurotrophin-3 were increased in the siRNA-1 group.No significant difference was found in cell migration between the negative control and siRNA-1 groups.Compared with the pGV230 group,the cell proliferation rate was down-regulated;apoptotic rate,p-c-Jun/c-Jun ratio and c-Fos protein expression increased;mRNA expression of protein kinase C alpha and Bax decreased;and mRNA expressions of neurotrophins basic fibroblast growth factor and neurotrophin-3 were up-regulated in the pGV230-Claudin-15 group.The above results demonstrated that overexpression of Claudin-15 inhibited Schwann cell proliferation and promoted Schwann cell apoptosis in vitro.Silencing of Claudin-15 had the reverse effect and provided neuroprotective effect.This study was approved by the Experimental Animal Ethics Committee of Jilin University of China(approval No.2016-nsfc001)on March 5,2016. Our previous experiments have discovered that Claudin-15 was up-regulated in Schwann cells of the distal nerve stumps of rat models of sciatic nerve injury. However, how Claudin-15 affects Schwann cell function is still unknown. This study aimed to identify the effects of Claudin-15 on proliferation and apoptosis of Schwann cells cultured in vitro and explore the underlying mechanisms. Primary Schwann cells were obtained from rats. Claudin-15 in Schwann cells was knocked down using siRNA(siRNA-1 group) compared with the negative control siRNA transfection group(negative control group). Claudin-15 in Schwann cells was overexpressed using pGV230-Claudin-15 plasmid(pGV230-Claudin-15 group). The pGV230 transfection group(pGV230 group) acted as the control of the pGV230-Claudin-15 group. Cell proliferation was analyzed with EdU assay. Cell apoptosis was analyzed with flow cytometric analysis. Cell migration was analyzed with Transwell inserts. The mRNA and protein expressions were analyzed with quantitative polymerase chain reaction assay and western blot assay. The results showed that compared with the negative control group, cell proliferation rate was up-regulated; p-AKT/AKT ratio, apoptotic rate, p-c-Jun/c-Jun ratio, mRNA expression of protein kinase C alpha, Bcl-2 and Bax were down-regulated; and mRNA expression of neurotrophins basic fibroblast growth factor and neurotrophin-3 were increased in the siRNA-1 group. No significant difference was found in cell migration between the negative control and siRNA-1 groups. Compared with the pGV230 group, the cell proliferation rate was down-regulated; apoptotic rate, p-c-Jun/c-Jun ratio and c-Fos protein expression increased; mRNA expression of protein kinase C alpha and Bax decreased; and mRNA expressions of neurotrophins basic fibroblast growth factor and neurotrophin-3 were up-regulated in the pGV230-Claudin-15 group. The above results demonstrated that overexpression of Claudin-15 inhibited Schwann cell proliferation and promoted Schwann cell apoptosis in vitro. Silencing of Claudin-15 had the reverse effect and provided neuroprotective effect. This study was approved by the Experimental Animal Ethics Committee of Jilin University of China(approval No. 2016-nsfc001) on March 5, 2016.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2020年第1期169-177,共9页 中国神经再生研究(英文版)
基金 supported by the National Natural Science Foundation of China,No.81671220(to SSC) the Scientific and Technological Development Program of Jilin Province of China,No.20160101077JC(to SSC) the School Joint Construction Special Project of Jilin Province of China,No.SXGJQY2017-13(to SSC)
关键词 apoptosis Bax cell PROLIFERATION c-Jun Claudin-15 NERVE regeneration peripheral NERVE injury protein kinase C alpha Schwann cells Wallerian DEGENERATION apoptosis Bax cell proliferation c-Jun Claudin-15 nerve regeneration peripheral nerve injury protein kinase C alpha Schwann cells Wallerian degeneration
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  • 1杜怀栋,周梁.神经导管在神经修复中的作用[J].复旦学报(医学版),2006,33(5):709-710. 被引量:5
  • 2Angelow S, Ahlstrom R, Yu AS (2008) Biology of claudins. Am J Physiol Renal Physio1295:F867-876.
  • 3Arthur Farraj PJ, Latouche M, Wilton DK, Quintes S, Chabrol E, Baner- jee A, Woodhoo A, Jenkins B, Rahman M, Turmaine M (2012) c-Jun reprograms Schwann cells of injured nerves to generate a repair cell essential for regeneration. Neuron 75:633-647.
  • 4Barrette B, Calvo E, Vallies N, Lacroix S (2010) Transcriptional profiling of the injured sciatic nerve carrying the WId(S) mutant gene: iden- tification of genes involved in neuroprotection, neuroinflammation, and nerve regeneration. Brain Behav Immun 24:1254-1267.
  • 5Ben Yosef T, Belyantseva IA, Saunders TL, Hughes E, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER (2003) Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet 12:2049-2061.
  • 6Boivin A, Pineau I, Barrette B, Filali M, Vallieres N, Rivest S, Lacroix S (2007) Toll-like receptor signaling is critical for Wallerian degenera- tion and functional recovery after peripheral nerve injury. J Neurosci 27:12565-12576.
  • 7Chattopadhyay S, Shubayev V (2009) MMP-9 controls Schwann cell proliferation and phenotypic remodeling via IGF-1 and ErbB recep- tor-mediated activation of MEK/ERK pathway. Glia 57:1316-1125.
  • 8De S, Trigueros MA, Kalyvas A, David S (2003) Phospholipase A2 plays an important role in myelin breakdown and phagocytosis during Wallerian degeneration. Mol Cell Neurosci 24:753-765.
  • 9Elkouby Naor L, Abassi Z, Lagzie A, Gow A, Ben-osef T (2008) Dou- ble gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins. Cell Tissue Res 333:427-438.
  • 10Feltri ML, Wrabetz L, Behrens A, Mirsky R, Jessen K (2008) c-Jun is a negative regulator of myelination. J Cell Biol 181:625-637.

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