观点评论

眼表疾病里的细胞衰老:机制与治疗视角

来源:Int J Mol Sci · PMID 42941778 · DOI 10.3390/ijms27209003** · 来源:IMA 知识库《文献层·文献监控卡片》2026-10-29 期 · 全文级(file_id dGBunAeRiRlm,下载实测 692,872 B) · 全文已获取并通过归属校验

数据日期 2026-10-29 · 生成时间 2026-10-29 06:03

研究问题

The ocular surface is an integrated functional unit comprising the tear film, cornea, conjunctiva, limbus, lacrimal and meibomian glands, eyelids, and associated neural and immune components [1,2].

方法

(全文无独立方法节,正文亦未给出可抽取的实验动作句)

核心结论

Its components include pro-inflammatory cytokines such as interleukin-1 alpha (IL-1α), interleukin-1 beta (IL-1β), IL-6, IL-8, and tumor necrosis factor-alpha (TNF-α); chemokines such as C-C motif chemokine ligand 2 (CCL2), C-C motif chemokine ligand 5 (CCL5), and C-X-C motif chemokine ligand 8 (CXCL8); growth factors such as transforming growth factor-β (TGF-β), vascular endothelial growth factor (VEGF), and granulocyte-macrophage colony-stimulating factor (GM-CSF); and matrix-remodeling enzymes such as MMP-1, MMP-3, and MMP-9 [12,36].;SASP-associated signaling can also propagate senescence to neighboring cells through IL-1α/NF-κB, signal transducer and activator of transcription 3 (STAT3), and TGF-β-related pathways, thereby contributing to the spatial expansion of senescence within tissues [10].;Senescence-associated beta-galactosidase (SA-β-gal) positivity and activation of the… ‖ 结论:Future studies should define disease- and cell-specific markers, use cell-resolved profiling to identify senescent populations, and test whether selective depletion or functional modulation improves disease outcomes.

局限

全文未设独立 limitations 节;结构上为综述/二次研究,因果推断强度受限。

对本项目的价值

★★★★☆ 细胞衰老清除/重编程是项目干预管线的核心支柱之一。命中核心 mTOR/AMPK;设计 多组学。

全文来源

PMC JATS 全文(正文 32,597 字符,已过标题/DOI 逐字归属校验)

原文题录

  • 英文标题:Cellular Senescence in Ocular Surface Diseases: Molecular Mechanisms and Therapeutic Perspectives.
  • 期刊与标识:Int J Mol Sci · PMID 42941778 · DOI 10.3390/ijms27209003**

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