Natural flavonoid glycosides Chrysosplenosides I & A rejuvenate intestinal stem cell aging via activation of PPARγ signaling

Jinbao Ye, La Yan, Yu Yuan, Fang Fu, Lu Yuan, Xinxin Fan, Juanyu Zhou, Yuedan Zhu, Xingzhu Liu, Gang Ren, Haiyang Chen

PDF(5341 KB)
PDF(5341 KB)
Life Medicine ›› 2024, Vol. 3 ›› Issue (3) : lnae025. DOI: 10.1093/lifemedi/lnae025
Article

Natural flavonoid glycosides Chrysosplenosides I & A rejuvenate intestinal stem cell aging via activation of PPARγ signaling

Author information +
History +

Abstract

The decline in intestinal stem cell (ISC) function is a hallmark of aging, contributing to compromised intestinal regeneration and increased incidence of age-associated diseases. Novel therapeutic agents that can rejuvenate aged ISCs are of paramount importance for extending healthspan. Here, we report on the discovery of Chrysosplenosides I and A (CAs 1 & 2), flavonol glycosides from the Xizang medicinal plant Chrysosplenium axillare Maxim., which exhibit potent anti-aging effects on ISCs. Our research, using Drosophila models, reveals that CAs 1 & 2 treatments not only restrain excessive ISC proliferation, thereby preserving intestinal homeostasis, but also extend the lifespan of aging Drosophila. In aged mouse intestinal organoids, CAs 1 & 2 enhance the growth and budding of intestinal organoids, indicating improved regenerative capacity. Mechanistic investigations show that CAs 1 & 2 exert their effects by activating the peroxisome proliferator-activated receptor-gamma (PPARγ) and concurrently inhibiting the epidermal growth factor receptor (EGFR) signaling pathways. Our findings position CAs 1 & 2 as promising candidates for ameliorating ISC aging and suggest that targeting PPARγ, in particular, may offer a therapeutic strategy to counteract age-related intestinal dysfunction.

Keywords

intestinal stem cell / aging / chrysosplenoside / Drosophila / PPAR

Cite this article

Download citation ▾
Jinbao Ye, La Yan, Yu Yuan, Fang Fu, Lu Yuan, Xinxin Fan, Juanyu Zhou, Yuedan Zhu, Xingzhu Liu, Gang Ren, Haiyang Chen. Natural flavonoid glycosides Chrysosplenosides I & A rejuvenate intestinal stem cell aging via activation of PPARγ signaling. Life Medicine, 2024, 3(3): lnae025 https://doi.org/10.1093/lifemedi/lnae025

References

[1]
Liu B , Qu J , Zhang W , et al. A stem cell aging framework, from mechanisms to interventions. Cell Rep 2022; 41: 111451.
CrossRef Google scholar
[2]
Götz M . Revising concepts about adult stem cells. Sci 2018; 359: 639- 40.
CrossRef Google scholar
[3]
Jasper H . Intestinal stem cell aging: origins and interventions. Annu Rev Physiol 2020; 82: 203- 26.
CrossRef Google scholar
[4]
Adams Peter D , Jasper H , Rudolph KL . Aging-induced stem cell mutations as drivers for disease and cancer. Cell Stem Cell 2015; 16: 601- 12.
CrossRef Google scholar
[5]
Ha CY , Katz S . Clinical implications of ageing for the management of IBD. Nat Rev Gastroenterol Hepatol 2013; 11: 128- 38.
CrossRef Google scholar
[6]
Zhu J , An Y , Wang X , et al. The natural product rotundic acid treats both aging and obesity by inhibiting PTP1B.Life Med. 2022; 1: 372- 86.
CrossRef Google scholar
[7]
Shah MA , Faheem HI , Hamid A , et al. The entrancing role of dietary polyphenols against the most frequent aging-associated diseases. Med Res Rev 2023; 44: 235- 74.
CrossRef Google scholar
[8]
Xu Q , Fu Q , Li Z , et al. The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice. Nat Metab 2021; 3: 1706- 26.
CrossRef Google scholar
[9]
Yan L , Guo X , Zhou J , et al. Quercetin prevents intestinal stem cell aging via scavenging ROS and inhibiting insulin signaling in Drosophila. Antioxidants 2022; 12: 59.
CrossRef Google scholar
[10]
Zhi-Ling Y , Chi Z , Hui-Qin G , et al. Isolation and identification of chemical constituents from Tibetan medicine “Ya-Ji-Ma” (Chrysosplenium axillare). Chinese Traditional and Herbal Drugs 2022; 53: 354- 61.
[11]
Cai Z , Li W , Jiang W , et al. Protective effect of the ethyl acetate fraction of Qinghai-Tibet Plateau medicinal plant Chrysosplenium axillare Maxim. against ANIT-induced cholestatic liver injury in mice. Phytomedicine Plus 2021; 1: 100076.
CrossRef Google scholar
[12]
Fox DT , Cohen E , Smith-Bolton R . Model systems for regeneration: Drosophila. Development 2020; 147: dev173781.
CrossRef Google scholar
[13]
Micchelli CA , Perrimon N . Evidence that stem cells reside in the adult Drosophila midgut epithelium. Nature 2005; 439: 475- 9.
CrossRef Google scholar
[14]
Hales KG , Korey CA , Larracuente AM , et al. Genetics on the fly: a primer on the Drosophila model system. Genetics 2015; 201: 815- 42.
CrossRef Google scholar
[15]
Ohlstein B , Spradling A . The adult Drosophila posterior midgut is maintained by pluripotent stem cells. Nature 2005; 439: 470- 4.
CrossRef Google scholar
[16]
Lu T-C , Brbić M , Park Y-J , et al. Aging Fly Cell Atlas identifies exhaustive aging features at cellular resolution. Sci 2023; 380: eadg0934.
CrossRef Google scholar
[17]
Clevers H . Modeling development and disease with organoids. Cell 2016; 165: 1586- 97.
CrossRef Google scholar
[18]
Zhao Q , Guan J , Wang X . Intestinal stem cells and intestinal organoids. J Genet Genomics 2020; 47: 289- 99.
CrossRef Google scholar
[19]
Choi NH , Kim JG , Yang DJ , et al. Age-related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF-like growth factor. Aging Cell 2008; 7: 318- 34.
CrossRef Google scholar
[20]
Nalapareddy K , Nattamai KJ , Kumar RS , et al. Canonical wnt signaling ameliorates aging of intestinal stem cells. Cell Rep 2017; 18: 2608- 21.
CrossRef Google scholar
[21]
Lin G , Xu N , Xi R . Paracrine Wingless signalling controls self-renewal of Drosophila intestinal stem cells. Nature 2008; 455: 1119- 23.
CrossRef Google scholar
[22]
Obata F , Tsuda-Sakurai K , Yamazaki T , et al. Nutritional control of stem cell division through S-Adenosylmethionine in Drosophila intestine. Dev Cell 2018; 44: 741- 51.e3.
CrossRef Google scholar
[23]
Vaccaro A , Kaplan Dor Y , Nambara K , et al. Sleep loss can cause death through accumulation of reactive oxygen species in the gut. Cell 2020; 181: 1307- 28.e15.
CrossRef Google scholar
[24]
Du G , Xiong L , Li X , et al. Peroxisome elevation induces stem cell differentiation and intestinal epithelial repair. Dev Cell 2020; 53: 169- 84.e11.
CrossRef Google scholar
[25]
Zhou Q , Yu L , Cook JR , et al. Deciphering the decline of metabolic elasticity in aging and obesity. Cell Metab 2023; 35: 1661- 71.e6.
CrossRef Google scholar
[26]
To KWK , Wu WKK , Loong HHF . PPARgamma agonists sensitize PTEN-deficient resistant lung cancer cells to EGFR tyrosine kinase inhibitors by inducing autophagy. Mol Cell Pharmacol 2018; 823: 19- 26.
CrossRef Google scholar
[27]
Oh J , Lee YD , Wagers AJ . Stem cell aging: mechanisms, regulators and therapeutic opportunities. Nat Med 2014; 20: 870- 80.
CrossRef Google scholar
[28]
Shen N , Wang T , Gan Q , et al. Plant flavonoids: classification, distribution, biosynthesis, and antioxidant activity. Food Chem 2022; 383: 132531.
CrossRef Google scholar
[29]
Ahmadian M , Suh JM , Hah N , et al. PPARγ signaling and metabolism: the good, the bad and the future. Nat Med 2013; 19: 557- 66.
CrossRef Google scholar
[30]
Korbecki J , Bobiński R , Dutka M . Self-regulation of the inflammatory response by peroxisome proliferator-activated receptors. Inflamm Res 2019; 68: 443- 58.
CrossRef Google scholar
[31]
Vallée A , Lecarpentier Y . Crosstalk between peroxisome proliferator-activated receptor gamma and the canonical WNT/β-catenin pathway in chronic inflammation and oxidative stress during carcinogenesis. Front Immunol 2018; 9: 745.
CrossRef Google scholar
[32]
Du G , Liu Z , Yu Z , et al. Taurine represses age-associated gut hyperplasia in Drosophila via counteracting endoplasmic reticulum stress. Aging Cell 2021; 20: e13319.
CrossRef Google scholar
[33]
Rodriguez-Fernandez IA , Tauc HM , Jasper H . Hallmarks of aging Drosophila intestinal stem cells. Mech Ageing Dev 2020; 190: 111285.
CrossRef Google scholar
[34]
Wu S-C , Cao Z-S , Chang K-M , et al. Intestinal microbial dysbiosis aggravates the progression of Alzheimer’s disease in Drosophila. Nat Commun 2017; 8: 24.
CrossRef Google scholar
[35]
Gorgulla C , Çınaroğlu SS , Fischer PD , et al. VirtualFlow ants—ultra-large virtual screenings with artificial intelligence driven docking algorithm based on ant colony optimization. Int J Mol Sci 2021; 22: 5807.
CrossRef Google scholar
[36]
Ji L , Song T , Ge C , et al. Identification of bioactive compounds and potential mechanisms of scutellariae radix-coptidis rhizoma in the treatment of atherosclerosis by integrating network pharmacology and experimental validation. Biomed Pharmacother 2023; 165: 115210.
CrossRef Google scholar
[37]
Eberhardt J , Santos-Martins D , Tillack AF , et al. AutoDock Vina 1.2.0: new docking methods, expanded force field, and python bindings. J Chem Inf Model 2021; 61: 3891- 8.
CrossRef Google scholar
[38]
Riyaphan J , Pham D-C , Leong MK , et al. In silico approaches to identify polyphenol compounds as α-glucosidase and α-amylase inhibitors against type-II diabetes. Biomolecules 2021; 11: 1877.
CrossRef Google scholar

RIGHTS & PERMISSIONS

2024 The Author(s). Published by Oxford University Press on behalf of Higher Education Press.
AI Summary AI Mindmap
PDF(5341 KB)

Accesses

Citations

Detail

Sections
Recommended

/