# Isaridin E Protects Against UVB-Induced Photoaging by Activating Wnt/β-Catenin Signaling Pathway and Alleviating Mitochondrial Dysfunction

**Authors:** Yaosheng Liu, Weizhen Li, Zeen Yang, Hui Long, Sufen Cai, Changjie Sun, Yu Xiong, Yunqi Zhang, Yumei Liu, Guangpu Luo, Senhua Chen, Tie Zhao

PMC · DOI: 10.3390/md24030112 · Marine Drugs · 2026-03-18

## TL;DR

Isaridin E, a marine compound, reduces UVB-induced skin aging by boosting Wnt/β-catenin signaling and improving mitochondrial health.

## Contribution

Isaridin E is shown to counteract photoaging through Wnt/β-catenin activation and mitochondrial protection, offering a novel therapeutic approach.

## Key findings

- Isaridin E restores fibroblast viability and reduces senescence markers in UVB-exposed cells.
- In mice, Isaridin E improves skin thickness and collagen levels while lowering SASP factors.
- Isaridin E activates the Wnt/β-catenin pathway and mitigates mitochondrial dysfunction.

## Abstract

Mitochondrial dysfunction is a major contributor to skin photoaging. Activation of the Wnt/β-catenin pathway, a key regulator of developmental processes, can improve mitochondrial abnormalities associated with pathology. Therefore, the Wnt/β-catenin pathway emerges as a key therapeutic target in the context of photoaging. Isaridin E (ISE), a marine-derived natural product with a novel structure, exhibits potent antiplatelet and anti-inflammatory activities. We sought to examine the anti-senescence effects of ISE on fibroblasts in photoaged skin. In vitro, ISE improved UVB-induced fibroblast damage in a dose-dependent manner, restoring cell viability, reducing β-galactosidase accumulation, and suppressing SASP factor production. In a photoaging mouse model, ISE markedly decreased skin thickness, increased dermal collagen expression, and reduced SASP levels in skin tissues. ISE significantly improved fibroblast energy production deficits and mitochondrial dysfunction. RNA sequencing and Western blotting demonstrated that UVB irradiation significantly suppressed Wnt/β-catenin signaling activity, whereas ISE dose-dependently restored pathway activation. Using GSK-3β-targeted siRNA, we showed that the anti-photoaging effects of ISE are mediated via the Wnt/β-catenin pathway. ISE appears to counteract photoaging by enhancing Wnt/β-catenin activity and improving mitochondrial function.

## Linked entities

- **Genes:** Wnt (protein Wnt-2) [NCBI Gene 100641115], ctnnb1.S (catenin beta 1 S homeolog) [NCBI Gene 380441], GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932]
- **Chemicals:** Isaridin E (PubChem CID 16680915), UVB (PubChem CID 154464873)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cdkn1a (cyclin dependent kinase inhibitor 1A) [NCBI Gene 12575] {aka CAP20, CDKI, CIP1, Cdkn1, P21, SDI1}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, Trp53-ps (transformation related protein 53, pseudogene) [NCBI Gene 22060], CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, Acsm3 (acyl-CoA synthetase medium-chain family member 3) [NCBI Gene 20216] {aka Sa, Sah}, Eln (elastin) [NCBI Gene 13717] {aka E030024M20Rik}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, Cdkn2a (cyclin dependent kinase inhibitor 2A) [NCBI Gene 12578] {aka ARF-INK4a, Arf, INK4a-ARF, Ink4a/Arf, MTS1, Pctr1}, Wnt2 (wingless-type MMTV integration site family, member 2) [NCBI Gene 22413] {aka 2610510E18Rik, Int1l1, Irp, Mirp, Wnt-2, Wnt2a}, H2ax (H2A.X variant histone) [NCBI Gene 15270] {aka H2A.X, H2afx, Hist5-2ax, gammaH2ax}, Atr (ataxia telangiectasia and Rad3 related) [NCBI Gene 245000], TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, Ndufa9 (NADH:ubiquinone oxidoreductase subunit A9) [NCBI Gene 66108] {aka 1010001N11Rik}, Atm (ataxia telangiectasia mutated) [NCBI Gene 11920] {aka C030026E19Rik}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Dapk2 (death-associated protein kinase 2) [NCBI Gene 13143], Glb1 (galactosidase, beta 1) [NCBI Gene 12091] {aka Bge, Bgl, Bgl-e, Bgl-s, Bgl-t, Bgs}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Mmp3 (matrix metallopeptidase 3) [NCBI Gene 17392] {aka EMS-2, MMP-3, SL-1, SLN-1, SLN1, STR-1}, Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 56637] {aka 7330414F15Rik, 8430431H08Rik, GSK-3, GSK-3beta, GSK3}, ND1 (NADH dehydrogenase subunit 1) [NCBI Gene 17716]
- **Diseases:** epidermal hyperplasia (MESH:D006965), thrombosis (MESH:D013927), inflammation (MESH:D007249), osteoporosis (MESH:D010024), Alzheimer's disease (MESH:D000544), sepsis (MESH:D018805), wrinkle (MESH:D019773), cancers (MESH:D009369), erythema (MESH:D004890), hypertrophic scars (MESH:D017439), water (MESH:D000069578), melanoma (MESH:D008545), Mitochondrial Dysfunction (MESH:D028361), basal cell carcinoma (MESH:D002280), cytotoxicity (MESH:D064420), fibroblast dysfunction (MESH:D006331), skin dryness (MESH:D014987), bleeding (MESH:D006470), injury to (MESH:D014947), ISE (MESH:D016751)
- **Chemicals:** MTT (MESH:C070243), Pro (MESH:D011392), N (MESH:D009584), hematoxylin (MESH:D006416), Tween 80 (MESH:D011136), CO2 (MESH:D002245), ATP (MESH:D000255), H&amp;E (MESH:D006371), SA (MESH:D000077145), DMSO (MESH:D004121), GSH (MESH:D005978), PBS (MESH:D007854), alpha-amino acid (MESH:D000596), 3-(4,5-Dimethylthiazol-2-YL)-2,5-Diphenyltetrazolium Bromide (MESH:C022616), JC-1 (MESH:C068624), NAD+ (MESH:D009243), ROS (MESH:D017382), amide (MESH:D000577), TRIzol (MESH:C411644), paraformaldehyde (MESH:C003043), formazan (MESH:D005562), SDS (MESH:D012967), eosin (MESH:D004801), cyclodepsipeptide (MESH:D047630), MDA (MESH:D008315), beta-Ala (MESH:D015091), 13C (MESH:C000615229), propylene glycol (MESH:D019946), PVDF (MESH:C024865), H (MESH:D006859), Phe (MESH:D010649), 1H (-), 2-hydroxy-4-methylpentanoic acid (MESH:C574291)
- **Species:** Styela plicata (species) [taxon 7726], Homo sapiens (human, species) [taxon 9606], Amphichorda felina (species) [taxon 37994], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028182/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028182/full.md

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Source: https://tomesphere.com/paper/PMC13028182