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SHED-exos 通过抑制 p-ERK1/2 介导的腺细胞凋亡来促进唾液分泌。

SHED-exos promote saliva secretion by suppressing p-ERK1/2-mediated apoptosis in glandular cells.

机构信息

Department of Periodontics, Shanxi Medical University School and Hospital of Stomatology, Taiyuan, Shanxi, P.R. China.

Center Laboratory, Peking University School and Hospital of Stomatology, Beijing, P.R. China.

出版信息

Oral Dis. 2024 Jul;30(5):3066-3080. doi: 10.1111/odi.14776. Epub 2023 Oct 17.

Abstract

OBJECTIVES

Confirm that stem cells from human exfoliated deciduous teeth-derived exosomes (SHED-exos) can limit inflammation-triggered epithelial cell apoptosis and explore the molecular mechanism.

METHODS

SHED-exos were injected into the submandibular glands (SMGs) of non-obese diabetic (NOD) mice, an animal model of Sjögren's syndrome (SS). Cell death was evaluated by western blotting and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling staining.

RESULTS

SHED-exos treatment promoted the saliva flow rates of NOD mice, accompanied by decreased cleaved caspase-3 levels and apoptotic cell numbers in SMGs. SHED-exos inhibited autophagy, pyroptosis, NETosis, ferroptosis, necroptosis and oxeiptosis marker expression in SS-damaged glands. Mechanistically, Kyoto Encyclopedia of Genes and Genomes analysis of exosomal miRNAs suggested that the rat sarcoma virus (RAS)/mitogen-activated protein kinase kinase (MEK)/extracellular signal-regulated kinase (ERK) pathway might play an important role. In vivo, the expression of Kirsten RAS, Harvey RAS, MEK1/2 and p-ERK1/2 was upregulated in SMGs, and this change was blocked by SHED-exos treatment. In vitro, SHED-exos suppressed p-ERK1/2 activation and increased cleaved caspase-3 and apoptotic cell numbers, which were induced by IFN-γ.

CONCLUSION

SHED-exos suppress epithelial cell death, which is responsible for promoting salivary secretion. SHED-exos inhibited inflammation-triggered epithelial cell apoptosis by suppressing p-ERK1/2 activation, which is involved in these effects.

摘要

目的

证实人脱落乳牙衍生的外泌体(SHED-exos)中的干细胞可以限制炎症触发的上皮细胞凋亡,并探讨其分子机制。

方法

将 SHED-exos 注射到非肥胖型糖尿病(NOD)小鼠的颌下腺(SMG)中,这是干燥综合征(SS)的动物模型。通过 Western blot 和末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记染色评估细胞死亡。

结果

SHED-exos 治疗可促进 NOD 小鼠的唾液流量,同时降低 SMG 中裂解的 caspase-3 水平和凋亡细胞数量。SHED-exos 抑制了 SS 损伤腺体中的自噬、细胞焦亡、NETosis、铁死亡、坏死性凋亡和氧化细胞凋亡标志物的表达。机制上,外泌体 miRNA 的京都基因与基因组百科全书分析表明,大鼠肉瘤病毒(RAS)/丝裂原活化蛋白激酶激酶(MEK)/细胞外信号调节激酶(ERK)通路可能发挥重要作用。在体内,SMG 中 K-RAS、H-RAS、MEK1/2 和 p-ERK1/2 的表达上调,而这一变化被 SHED-exos 治疗所阻断。在体外,SHED-exos 抑制了 IFN-γ诱导的 p-ERK1/2 激活,增加了裂解的 caspase-3 和凋亡细胞数量。

结论

SHED-exos 抑制上皮细胞死亡,从而促进唾液分泌。SHED-exos 通过抑制 p-ERK1/2 激活来抑制炎症触发的上皮细胞凋亡,这涉及到这些作用。

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