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Protective Effect of Hydroxysafflor Yellow A on MSCs Against Senescence Induced by -galactose

Overview
Journal Chin Herb Med
Publisher Elsevier
Date 2023 Mar 6
PMID 36875432
Authors
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Abstract

Objective: To examine the protective effects of hydroxysafflor yellow A (HSYA) against the senescence of mesenchymal stem cells (MSCs) induced by -galactose (-gal) , and investigate the potential mechanism involved.

Methods: Grouping experiment, Normal control (NC) group: conventional culture with complete medium; Senescence group: MSCs were cultured for 48 h with complete medium containing 10 g/L -gal; HSYA group: on the basis of senescence induction, HSYA with the suitable concentration was used to protect MSCs. The key experimental indices associated with oxidative stress, inflammatory response, cell senescence, proliferation and apoptosis were measured through chemical colorimetry, β-galactosidase staining, EdU incorporation and flow cytometry, respectively. The relative quantity (RQ) of proteins related closely to cell proliferation, apoptosis, and NF-κB signaling were measured by Western blotting.

Results: As compared with Senescence group, treatment with HSYA (120 mg/L) effectively ameliorated the adverse situation of MSCs. Oxidation stress and inflammation along with -Gal induction was dramatically alleviated in MSCs; The β-Gal-positive staining indicated that MSC senescence was significantly mitigated; The proliferative capability of MSCs was significantly increased by up-regulating PCNA and inhibiting p16 expression; The anti-apoptotic effect on MSCs was exerted by down-regulating the RQ of cleaved Caspase-3 and Bax; The activity of NF-κB signaling in MSCs was notably suppressed through inhibiting phosphorylation of IKKβ and p65.

Conclusion: HSYA (120 mg/L) significantly delayed the -Gal-induced senescence process in MSCs through attenuating inflammatory reaction and oxidative stress, and suppressing the activity of NF-κB signaling.

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References
1.
Cai Y, Sukhova G, Wong H, Xu A, Tergaonkar V, Vanhoutte P . Rap1 induces cytokine production in pro-inflammatory macrophages through NFκB signaling and is highly expressed in human atherosclerotic lesions. Cell Cycle. 2015; 14(22):3580-92. PMC: 4825742. DOI: 10.1080/15384101.2015.1100771. View

2.
Guerrero A, De Strooper B, Arancibia-Carcamo I . Cellular senescence at the crossroads of inflammation and Alzheimer's disease. Trends Neurosci. 2021; 44(9):714-727. DOI: 10.1016/j.tins.2021.06.007. View

3.
Min F, Sun H, Wang B, Ahmad N, Guo H, Gao H . Hepatoprotective effects of hydroxysafflor yellow A in D-galactose-treated aging mice. Eur J Pharmacol. 2020; 881:173214. DOI: 10.1016/j.ejphar.2020.173214. View

4.
Wang Y, Zhang C, Peng W, Xia Z, Gan P, Huang W . Hydroxysafflor yellow A exerts antioxidant effects in a rat model of traumatic brain injury. Mol Med Rep. 2016; 14(4):3690-6. PMC: 5042747. DOI: 10.3892/mmr.2016.5720. View

5.
Lei L, Chen J, Zhao Y, Yang S, He L . Resveratrol attenuates senescence of adipose-derived mesenchymal stem cells and restores their paracrine effects on promoting insulin secretion of INS-1 cells through Pim-1. Eur Rev Med Pharmacol Sci. 2016; 20(6):1203-13. View