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本文引用的文献

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Adiponectin preserves metabolic fitness during aging.脂联素在衰老过程中保持代谢健康。
Elife. 2021 Apr 27;10:e65108. doi: 10.7554/eLife.65108.
2
Puerarin blocks the aging phenotype in human dermal fibroblasts.葛根素阻止人真皮成纤维细胞的衰老表型。
PLoS One. 2021 Apr 22;16(4):e0249367. doi: 10.1371/journal.pone.0249367. eCollection 2021.
3
Aging-dependent regulatory cells emerge in subcutaneous fat to inhibit adipogenesis.衰老相关调节细胞出现在皮下脂肪中,以抑制脂肪生成。
Dev Cell. 2021 May 17;56(10):1437-1451.e3. doi: 10.1016/j.devcel.2021.03.026. Epub 2021 Apr 19.
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Deletion of Nrip1 delays skin aging by reducing adipose-derived mesenchymal stem cells (ADMSCs) senescence, and maintaining ADMSCs quiescence.Nrip1 的缺失通过减少脂肪来源的间充质干细胞 (ADMSCs) 的衰老,从而延缓皮肤衰老,并维持 ADMSCs 的静止状态。
Geroscience. 2021 Aug;43(4):1815-1833. doi: 10.1007/s11357-021-00344-y. Epub 2021 Mar 11.
5
Lipid metabolic Reprogramming: Role in Melanoma Progression and Therapeutic Perspectives.脂质代谢重编程:在黑色素瘤进展中的作用及治疗前景
Cancers (Basel). 2020 Oct 27;12(11):3147. doi: 10.3390/cancers12113147.
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CD36 facilitates fatty acid uptake by dynamic palmitoylation-regulated endocytosis.CD36 通过动态棕榈酰化调控的内吞作用促进脂肪酸摄取。
Nat Commun. 2020 Sep 21;11(1):4765. doi: 10.1038/s41467-020-18565-8.
7
Dermal adipocytes contribute to the metabolic regulation of dermal fibroblasts.真皮脂肪细胞有助于调节真皮成纤维细胞的代谢。
Exp Dermatol. 2021 Jan;30(1):102-111. doi: 10.1111/exd.14181. Epub 2020 Sep 15.
8
Lipid Players of Cellular Senescence.细胞衰老中的脂质相关因素
Metabolites. 2020 Aug 21;10(9):339. doi: 10.3390/metabo10090339.
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Metabolic regulation of dermal fibroblasts contributes to skin extracellular matrix homeostasis and fibrosis.皮肤成纤维细胞的代谢调节有助于皮肤细胞外基质的稳态和纤维化。
Nat Metab. 2019 Jan;1(1):147-157. doi: 10.1038/s42255-018-0008-5. Epub 2019 Jan 7.
10
Changes in Aged Fibroblast Lipid Metabolism Induce Age-Dependent Melanoma Cell Resistance to Targeted Therapy via the Fatty Acid Transporter FATP2.衰老成纤维细胞脂质代谢的改变通过脂肪酸转运蛋白 FATP2 诱导与年龄相关的黑色素瘤细胞对靶向治疗的耐药性。
Cancer Discov. 2020 Sep;10(9):1282-1295. doi: 10.1158/2159-8290.CD-20-0329. Epub 2020 Jun 4.

皮肤衰老:真皮脂肪细胞代谢重编程真皮成纤维细胞。

Skin aging: Dermal adipocytes metabolically reprogram dermal fibroblasts.

机构信息

Scientific Department, Wellcomet GmbH, Karlsruhe, Germany.

Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

Bioessays. 2022 Jan;44(1):e2100207. doi: 10.1002/bies.202100207. Epub 2021 Nov 12.

DOI:10.1002/bies.202100207
PMID:34766637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8688300/
Abstract

Emerging data connects the aging process in dermal fibroblasts with metabolic reprogramming, provided by enhanced fatty acid oxidation and reduced glycolysis. This switch may be caused by a significant expansion of the dermal white adipose tissue (dWAT) layer in aged, hair-covered skin. Dermal adipocytes cycle through de-differentiation and re-differentiation. As a result, there is a strongly enhanced release of free fatty acids into the extracellular space during the de-differentiation of dermal adipocytes in the catagen phase of the hair follicle cycle. Both caveolin-1 and adiponectin are critical factors influencing these processes. Controlling the expression levels of these two factors also offers the ability to manipulate the metabolic preferences of the different cell types within the microenvironment of the skin, including dermal fibroblasts. Differential expression of adiponectin and caveolin-1 in the various cell types may also be responsible for the cellular metabolic heterogeneity within the cells of the skin.

摘要

新兴数据将真皮成纤维细胞的衰老过程与代谢重编程联系起来,这是由增强的脂肪酸氧化和减少的糖酵解提供的。这种转变可能是由于在有毛发覆盖的老年皮肤中,真皮白色脂肪组织 (dWAT) 层的显著扩张引起的。真皮脂肪细胞经历去分化和再分化。结果,在毛囊周期的退行期,真皮脂肪细胞去分化时,细胞外空间中游离脂肪酸的释放强烈增强。窖蛋白-1 和脂联素都是影响这些过程的关键因素。控制这两个因素的表达水平也提供了操纵皮肤微环境中不同细胞类型(包括真皮成纤维细胞)代谢偏好的能力。脂联素和窖蛋白-1在不同细胞类型中的差异表达也可能是皮肤细胞内细胞代谢异质性的原因。