Lactobacillus reuteri NCHBL-005 improves wound healing by promoting the activation of fibroblasts through TLR2/MAPK signaling.

Dong-Yeon Kim, Tae-Sung Lee, Yun-Ji Lee, So-Yeon Ahn, Byeongsam Chu, Do-Hyeon Jung, Yeong-Jun Kim, In-Su Seo, Wan-Gyu Kim, Young Jin Cho, Jung Joo Hong, Jong-Hwan Park
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Abstract

Background: Wound healing is a complex physiological process essential for restoring tissue integrity following various injuries, ranging from minor, everyday incidents to post-surgical complications. Emerging studies have demonstrated that lactic acid bacteria (LAB) can offer benefits beyond gut health, extending their positive effects on skin health. This study investigated the potential of Lactobacillus reuteri NCHBL-005, a honeybee-derived probiotic strain, to enhance fibroblast-mediated wound healing.

Method: L929 cells and mouse embryonic fibroblasts (MEFs) were utilized as models to specifically target fibroblasts. To assess the wound healing potential in vitro, a scratch assay was performed, providing insights into wound closure. Additionally, we created wound models in mice to evaluate the in vivo effects of the treatment.

Results: Our results showed that L. reuteri NCHBL-005 significantly accelerated wound closure in L929 fibroblast compared to other lactobacilli and exhibited superior efficacy in activating the mitogen-activated protein kinase (MAPK) pathway. Through MAPK inhibition assays, we confirmed that the wound healing effects of L. reuteri NCHBL-005 were MAPK-dependent, promoting fibroblast proliferation and differentiation. Notably, L. reuteri NCHBL-005 treatment did not facilitate wound healing in MEF cells derived from Toll-like-receptor 2 knockout (TLR2-/-) mice, highlighting the critical role of TLR2 in this mechanism. In vivo studies further corroborated these findings, in which topical administration of L. reuteri NCHBL-005 enhanced wound healing and stimulated fibroblast proliferation and activation, as confirmed by histopathological analysis.

Conclusion: These findings revealed that L. reuteri NCHBL-005 activates fibroblasts through TLR2 stimulation and subsequent MAPK pathway activation, suggesting its potential as a promising therapeutic candidate for wound management.

罗伊氏乳杆菌NCHBL-005通过TLR2/MAPK信号通路促进成纤维细胞的激活,从而促进伤口愈合。
背景:伤口愈合是一个复杂的生理过程,对于各种损伤(从轻微的日常事件到术后并发症)后恢复组织完整性至关重要。新兴研究表明,乳酸菌(LAB)可以提供肠道健康以外的益处,延伸其对皮肤健康的积极影响。本研究调查了罗伊氏乳杆菌NCHBL-005(一种蜜蜂来源的益生菌菌株)促进成纤维细胞介导的伤口愈合的潜力。方法:以L929细胞和小鼠胚胎成纤维细胞(MEFs)为模型,特异性靶向成纤维细胞。为了评估伤口在体外的愈合潜力,进行了划痕试验,为伤口愈合提供了见解。此外,我们在小鼠身上建立了伤口模型来评估治疗的体内效果。结果:我们的研究结果表明,与其他乳酸菌相比,罗伊氏乳杆菌nchcl -005显著加速L929成纤维细胞的伤口愈合,并在激活丝裂原活化蛋白激酶(MAPK)途径方面表现出优越的功效。通过MAPK抑制实验,我们证实罗伊氏乳杆菌nchcl -005的创面愈合作用依赖于MAPK,促进成纤维细胞增殖和分化。值得注意的是,罗伊氏乳杆菌NCHBL-005治疗并没有促进toll样受体2敲除(TLR2-/-)小鼠MEF细胞的伤口愈合,突出了TLR2在这一机制中的关键作用。体内研究进一步证实了这些发现,经组织病理学分析证实,局部给药罗伊氏乳杆菌NCHBL-005可促进伤口愈合,刺激成纤维细胞增殖和活化。结论:这些研究结果表明,罗伊氏乳杆菌NCHBL-005通过TLR2刺激和随后的MAPK通路激活来激活成纤维细胞,这表明它可能是一种有希望的伤口治疗候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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