PMID- 32922601 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200916 IS - 1936-2625 (Electronic) IS - 1936-2625 (Linking) VI - 13 IP - 8 DP - 2020 TI - Correlations of SDF-1 and CXCR4 levels with caspase-3 expression in the retina of rats after optic nerve injury. PG - 2058-2064 AB - OBJECTIVE: This study explores the correlations of stromal cell-derived factor-1 (SDF-1) and CXC chemokine receptor 4 (CXCR4) levels with caspase-3 expression in the retina of rats after optic nerve injury. MATERIALS AND METHODS: A total of 24 adult healthy specific pathogen-free Sprague-Dawley rats were selected and randomly divided into an optic nerve injury group (n=16) and an optic nerve sham-injury group (n=8). The optic nerve injury group was further sub-divided into a 3 d group (n=8) and a 7 d group (n=8) after their injuries. In the optic nerve injury group, the left eye of each rat was removed and prepared for the optic nerve injury model using the optic nerve clamping method. In the sham-injury group, the optic nerve in the left eye was only exposed without being clamped. The rats were sacrificed at 3 d and 7 d after their optic nerve injuries, and the retina was isolated. The expressions of SDF-1, CXCR4, and caspase-3 in the retina of the rats in each group were measured using an immunohistochemical method. Messenger ribonucleic acid (mRNA) and the protein expressions of SDF-1, CXCR4, and caspase-3 (cleaved caspase-3) in the retinas of rats were measured using quantitative real-time polymerase chain reaction (qPCR) and western blotting, respectively. Moreover, the correlations of the expression of SDF-1 and CXCR4 with caspase-3 expression were analyzed using the Spearman method. The apoptosis of retinal ganglion cells of rats in each group was observed using terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining. RESULTS: Immunohistochemistry of the retinas revealed that, compared with those in the sham-injury group, the expressions of SDF-1 and CXCR4 in the retina in the 3 d group and the 7 d group were gradually increased. Caspase-3 expression was significantly elevated at 3 d after the injuries, but obviously decreased at 7 d after the injuries. The results of qPCR showed that the relative expression levels of SDF-1 and CXCR4 mRNA in the retina at 3 d and 7 d after optic nerve injuries were also significantly higher than those in the sham-injury group (P<0.01), and the caspase-3 mRNA expression was initially increased at 3 d but reduced at 7 d after the injuries (P<0.01). Western blotting for the detection of the SDF-1, CXCR4 and caspase-3 proteins indicated changes similar to those of the qPCR. Spearman analysis results demonstrated that there was a positive correlation between the SDF-1 and CXCR4 expressions, but the expressions of SDF-1 and CXCR4 had negative correlations with caspase-3 expression. TUNEL staining showed that apoptosis of the retinal cells was increased in the 3 d group but significantly decreased in the 7 d group. CONCLUSION: After optic nerve injury, the continuous increase of the SDF-1 and CXCR4 levels suppresses the apoptosis of retinal cells and repairs the retina by inhibiting the cleavage activation of caspase-3. This provides new insights for the ongoing treatment of optic nerve injury. CI - IJCEP Copyright (c) 2020. FAU - Zhang, Xi AU - Zhang X AD - Departmental Health Check Section, Ningbo Eye Hospital Ningbo, Zhejiang, China. FAU - Liao, Yanhong AU - Liao Y AD - Departmental Health Check Section, Ningbo Eye Hospital Ningbo, Zhejiang, China. FAU - Ye, Ting AU - Ye T AD - Departmental Health Check Section, Ningbo Eye Hospital Ningbo, Zhejiang, China. LA - eng PT - Journal Article DEP - 20200801 PL - United States TA - Int J Clin Exp Pathol JT - International journal of clinical and experimental pathology JID - 101480565 PMC - PMC7476942 OTO - NOTNLM OT - CXCR4 OT - Optic nerve injury OT - SDF-1 OT - apoptosis OT - caspase-3 COIS- None. EDAT- 2020/09/15 06:00 MHDA- 2020/09/15 06:01 PMCR- 2020/08/01 CRDT- 2020/09/14 05:51 PHST- 2020/02/23 00:00 [received] PHST- 2020/03/27 00:00 [accepted] PHST- 2020/09/14 05:51 [entrez] PHST- 2020/09/15 06:00 [pubmed] PHST- 2020/09/15 06:01 [medline] PHST- 2020/08/01 00:00 [pmc-release] PST - epublish SO - Int J Clin Exp Pathol. 2020 Aug 1;13(8):2058-2064. eCollection 2020.