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1
Human cerebrospinal fluid microRNA: temporal changes following subarachnoid hemorrhage.人类脑脊液微小RNA:蛛网膜下腔出血后的时间变化
Physiol Genomics. 2016 May;48(5):361-6. doi: 10.1152/physiolgenomics.00052.2015. Epub 2016 Mar 4.
2
The comparison of microRNA profile of the dermis between the young and elderly.年轻人与老年人真皮组织中微小RNA表达谱的比较。
J Dermatol Sci. 2016 May;82(2):75-83. doi: 10.1016/j.jdermsci.2016.01.005. Epub 2016 Jan 31.
3
Aging rather than sun exposure is a major determining factor for the density of miR-125b-positive epidermal stem cells in human skin.衰老而非阳光照射是人类皮肤中miR-125b阳性表皮干细胞密度的主要决定因素。
Pathol Int. 2015 Aug;65(8):415-9. doi: 10.1111/pin.12320. Epub 2015 Jun 17.
4
UVA and UVB irradiation differentially regulate microRNA expression in human primary keratinocytes.UVA 和 UVB 辐射对人原代角质形成细胞中 microRNA 表达的差异调节。
PLoS One. 2013 Dec 31;8(12):e83392. doi: 10.1371/journal.pone.0083392. eCollection 2013.
5
Elevated miR-34c-5p mediates dermal fibroblast senescence by ultraviolet irradiation.紫外线照射通过升高 miR-34c-5p 介导真皮成纤维细胞衰老。
Int J Biol Sci. 2013 Aug 9;9(7):743-52. doi: 10.7150/ijbs.5345. eCollection 2013.
6
MicroRNAs in skin response to UV radiation.皮肤对紫外线辐射的反应中的 microRNAs。
Curr Drug Targets. 2013 Sep;14(10):1128-34. doi: 10.2174/13894501113149990184.
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MicroRNA-22 promotes cell survival upon UV radiation by repressing PTEN.MicroRNA-22 通过抑制 PTEN 促进紫外线辐射后的细胞存活。
Biochem Biophys Res Commun. 2012 Jan 6;417(1):546-51. doi: 10.1016/j.bbrc.2011.11.160. Epub 2011 Dec 7.
8
Squamous cell carcinoma of the skin shows a distinct microRNA profile modulated by UV radiation.皮肤鳞状细胞癌呈现出一种由紫外线辐射调节的独特微小RNA谱。
J Invest Dermatol. 2010 Nov;130(11):2686-9. doi: 10.1038/jid.2010.169. Epub 2010 Jun 24.
9
MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response.微小RNA介导的基因沉默调节紫外线诱导的DNA损伤反应。
EMBO J. 2009 Jul 22;28(14):2090-9. doi: 10.1038/emboj.2009.156. Epub 2009 Jun 18.
10
Clinical implications of aging skin: cutaneous disorders in the elderly.衰老皮肤的临床意义:老年人的皮肤疾病
Am J Clin Dermatol. 2009;10(2):73-86. doi: 10.2165/00128071-200910020-00001.

慢性 UVB 辐射后皮肤生物力学和 miRNA 表达。

Skin Biomechanics and miRNA Expression Following Chronic UVB Irradiation.

机构信息

Department of Materials Science and Engineering, The Ohio State University, Columbus, Ohio.

Department of Pathology, The Wexner Medical Center at The Ohio State University, Columbus, Ohio.

出版信息

Adv Wound Care (New Rochelle). 2020 Mar 1;9(3):79-89. doi: 10.1089/wound.2019.1034. Epub 2020 Jan 24.

DOI:10.1089/wound.2019.1034
PMID:31993250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6985774/
Abstract

Exposure to ultraviolet (UV) light from the sun is known to accelerate the skin aging process and leads to significant alterations in skin biomechanics; however, the molecular mechanisms by which chronic UVB affects biomechanical properties of the skin have not been well described. A murine model for chronic UVB exposure was used to examine changes in epidermal barrier function, skin biomechanics, and miRNA expression as a result of UVB. UVB irradiation caused skin to be weaker, less elastic, stiffer, and less pliable. Notably, these changes were not reversed after a 5-week period of recovery. Following UVB exposure, dermal collagen fibrils were significantly smaller in diameter and expression of the miR-34 family was significantly increased. To our knowledge, this is the first study to concurrently examine alterations in skin function, miRNA expression, and tissue biomechanics in response to chronic UVB exposure. The data suggest that UVB alters miR-34 family expression in skin, in addition to dysregulating collagen structure with subsequent reductions in strength and elasticity. miRNAs may play a pivotal role in regulating extracellular matrix deposition and skin biomechanics following chronic UVB exposure, and thus may be a possible target for therapeutic development. However, additional studies are needed to directly probe the link between UVB exposure, miRNA production, and skin biomechanics.

摘要

已知暴露于太阳的紫外线 (UV) 光会加速皮肤衰老过程,并导致皮肤生物力学发生重大变化;然而,慢性 UVB 影响皮肤生物力学特性的分子机制尚未得到很好的描述。本研究使用慢性 UVB 暴露的小鼠模型,研究了 UVB 导致表皮屏障功能、皮肤生物力学和 miRNA 表达变化的情况。UVB 照射会使皮肤变得脆弱、弹性降低、硬度增加、柔韧性降低。值得注意的是,这些变化在 5 周的恢复期后并未得到逆转。UVB 暴露后,真皮胶原纤维的直径明显变小,miR-34 家族的表达明显增加。据我们所知,这是第一项同时研究慢性 UVB 暴露对皮肤功能、miRNA 表达和组织生物力学变化的研究。数据表明,UVB 除了扰乱胶原蛋白结构导致强度和弹性降低外,还会改变皮肤中 miR-34 家族的表达。miRNA 可能在慢性 UVB 暴露后调节细胞外基质沉积和皮肤生物力学中发挥关键作用,因此可能成为治疗开发的一个潜在靶点。但是,需要更多的研究来直接探究 UVB 暴露、miRNA 产生和皮肤生物力学之间的联系。