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Skin ageing accelerates systemic ageing and impairs the body's disease resistance. Inflammaging is a significant contributor to skin ageing. However, the mechanism by which inflammatory factors contribute to skin ageing remains unclear. We conducted screenings and identified CXC motif chemokine ligand 10 (CXCL10) as an inducer of skin ageing, which can be effectively inhibited by magnolin extracted from Magnolia biondii flower. Our results show that CXCL10 not only enhances beta-galactosidase (β-gal) activity but also upregulates the expression of p21/p16, along with matrix metalloproteinases (MMP1, MMP9 and MMP10), through activation of the C-X-C motif chemokine receptor 3 (CXCR3) in human primary fibroblasts. These findings suggest that CXCL10 drives skin ageing by inducing cellular senescence and extracellular matrix degradation. Importantly, treatment with magnolin significantly mitigates skin ageing phenotypes induced by CXCL10 via the p38 signalling pathway. Furthermore, our study demonstrates that magnolin significantly mitigates UV-induced skin ageing in ex vivo human skin samples as well as on human facial skin. This study provides insight into the role of chemokine CXCL10 in promoting inflammaging and proposes an innovative approach for preventing and treating skin ageing.
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http://dx.doi.org/10.1111/jcmm.70507 | DOI Listing |
J Allergy Clin Immunol
September 2025
State Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Shanghai, China; University of Chinese Academy of Sciences, Beijing, China. Electronic address:
Background: Keratinocytes form the skin's first line of defense, not only serving as a physical barrier but also actively communicating with immune cells and sensory neurons.
Objective: To elucidate the molecular mechanisms by which keratinocytes contribute to barrier dysfunction and neuroimmune activation in atopic dermatitis (AD).
Methods: CB2R expression was assessed by RNA-seq, qRT-PCR, RNAscope fluorescence, and western blot.
Cell Chem Biol
September 2025
Department of Biological Sciences, College of Natural Science, Seoul National University, Seoul 08826, South Korea. Electronic address:
The nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (NLRP3) inflammasome detects a broad spectrum of pathogen- and damage-associated molecular patterns (PAMPs and DAMPs), initiating inflammatory responses through caspase-1 activation and interleukin (IL)-1β/IL-18 release. Dysregulated NLRP3 activation is implicated in a range of diseases, including infectious diseases, autoinflammatory disorders, metabolic disorders, and cancer, making it an attractive therapeutic target. Here, we identify ZAP-180013 as a potent and selective small-molecule inhibitor of NLRP3 through high-throughput chemical screening.
View Article and Find Full Text PDFEndocr Rev
September 2025
Departments of Nutrition, Biochemistry and Molecular Medicine, University of Montreal, and Montreal Diabetes Research Center, Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC, Canada.
Glycerol and glycerol-3-phosphate are key metabolites at the intersection of carbohydrate, lipid and energy metabolism. Their production and usage are organismal and cell type specific. Glycerol has unique physicochemical properties enabling it to function as an osmolyte, protein structure stabilizer, antimicrobial and antifreeze agent, important to preservation of many biological functions.
View Article and Find Full Text PDFResearch (Wash D C)
September 2025
NHC Key Laboratory of Tropical Disease Control, School of Life Sciences and Medical Technology, Hainan Medical University, Haikou, Hainan 571199, China.
Aging is characterized by a gradual decline in the functionality of all the organs and tissues, leading to various diseases. As the global population ages, the urgency to develop effective anti-aging strategies becomes increasingly critical due to the growing severity of associated health problems. Immunotherapy offers novel and promising approaches to combat aging by utilizing approaches including vaccines, antibodies, and cytokines to target specific aging-related molecules and pathways.
View Article and Find Full Text PDFJID Innov
November 2025
Department of Dermatology, Graduate School of Medicine, Osaka University, Suita, Japan.
Previous studies have revealed that skin T cells accumulate and maintain immune responses in the elderly. However, we questioned why these functional T cells fail to recognize and eliminate malignant cells, making elderly skin more prone to developing malignant tumors. To address this question, we examined the overall skin microenvironment in aging using the Nanostring nCounter system and 10x Xenium digital spatial RNA sequencing.
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