治疗角膜碱损伤新方法的第一步:富含血小板的纤维蛋白裂解物对氢氧化钠暴露的兔角膜缘干细胞增殖的影响

Wahyu Endah Prabawati, Gatut Suhendro, E. Retnowati
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引用次数: 2

摘要

亮点:氢氧化钠引起富含血小板的纤维蛋白在化学创伤中刺激角膜缘干细胞增殖。富含血小板的纤维蛋白修复角膜缘干细胞生态位并影响角膜缘干度。摘要:眼部化学损伤会对眼表和角膜缘干细胞造成广泛损伤,导致永久性单侧或双侧视觉损伤。碱损伤比酸损伤更常见。血小板是潜在伤口愈合的丰富来源,促进多肽生长因子。本研究旨在研究富含血小板的纤维蛋白(PRF)裂解物对角膜缘干细胞增殖的影响,该细胞暴露于氢氧化钠中,类似于由于化学创伤导致的角膜缘干电池缺乏。用富含血小板的纤维蛋白裂解物(PRF)(0、5和10%)处理使用20µL 0.00625 M氢氧化钠(pH 13)损伤的融合兔(Oryctolagus cuniculus)角膜缘干细胞。根据Choukroun的方法从外周兔血中制备PRF裂解物,不使用抗凝剂和外来因子进行血小板活化。角膜缘干细胞的增殖在暴露于氢氧化钠后24、48和72小时通过3-(4,5-二甲基噻唑-2-基)-2.50二苯基溴化四氮唑(MTT)比色法测定。用5%的PRF裂解物使角膜缘干细胞的增殖显著增加(p0.01)。在氢氧化钠模型引起的化学损伤中,PRF刺激角膜缘干干细胞增殖。PRF修复角膜缘干细胞生态位,影响角膜缘干度。目前的发现值得进一步研究PRF作为一种治疗角膜缘干细胞缺乏症的新的替代疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A First Step to Novel Approach for Treating Alkali Injury of the Cornea: Effect of Platelet Rich Fibrin Lysates on Cultured Rabbit (Oryctolagus cuniculus) Limbal Stem Cell Proliferation Exposed by Sodium Hydroxide
Highlights: Sodium hydroxide causing platelet rich fibrin stimulates limbal stem cell proliferation in chemical trauma. Limbal stem cell niche and influences limbal stemness was repaired by Platelet Rich Fibrin.   Abstract: Chemical injuries of the eye produce extensive damage to the ocular surface and limbal stem cells, resulting in permanent unilateral or bilateral visual impairment. Alkali injuries occur more frequently than acid injuries. Platelets are a rich source of potential wound healing, promoting polypeptide growth factors. This study aimed to investigate the effect of platelet-rich fibrin (PRF) lysates on limbal stem cell proliferation, which was exposed to sodium hydroxide that resembled limbal stem cell deficiency due to chemical trauma. Confluent rabbit (Oryctolagus cuniculus) limbal stem cells wounded using 20µL of 0.00625 M sodium hydroxide (pH 13) were treated with platelet-rich fibrin lysates (PRF) (0, 5, and 10%). PRF lysates were prepared from peripheral rabbit blood according to Choukroun's method without using anticoagulant and foreign factors for platelet activation. The proliferation of limbal stem cells was measured by a 3-(4,5-dimethylthiazol-2-yl)-2.50 diphenyl tetrazolium bromide (MTT) colorimetric assay at 24, 48, and 72 hours after exposure to sodium hydroxide. Proliferation significantly increased limbal stem cells with PRF lysates 5% (p<0.01) and 10% (p<0.01) group compared with the control (PRF 0%). There was no significant difference between PRF lysates of 5% and 10% (p>0.01). The highest proliferation of limbal stem cells was found in the PRF lysates 5% group after 48 hours (100.24%). PRF stimulated limbal stem cell proliferation in chemical trauma caused by the sodium hydroxide model. PRF repaired the limbal stem cell niche and influenced the limbal stemness. The present findings warrant further research on PRF as a novel alternative treatment for limbal stem cell deficiency.
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