# Argan Callus Extract Restores Skin Cells via AMPK-Dependent Regulation of Energy Metabolism, Autophagy, and Inflammatory Pathways

**Authors:** Ramona Hartinger, Felix Quirin Fenzl, Vanessa Martina Nalewaja, Karima Djabali

PMC · DOI: 10.3390/antiox14070804 · Antioxidants · 2025-06-28

## TL;DR

Argan callus extract helps restore skin cell function by reducing aging signs and supporting stem cells through energy and inflammation regulation.

## Contribution

The study reveals the novel mechanism of argan callus extract in restoring skin cell health via AMPK-dependent pathways.

## Key findings

- PC treatment reduced cellular senescence and oxidative stress in fibroblasts and stem cells.
- PC enhanced ATP production, autophagy, and preserved stemness markers in skin-derived precursor cells.
- PC showed antioxidant and anti-aging properties by inhibiting elastase and reducing inflammation.

## Abstract

Skin aging is driven by cellular senescence, oxidative stress, and diminished regenerative capacity. In this study, we investigated the effects of PhytoCellTec™ Argan, an argan callus extract (PC), on primary human fibroblasts and adult stem cells. PC treatment (0.1% and 0.5%) significantly enhanced fibroblast proliferation, reduced senescence-associated β-galactosidase activity, and decreased the expression of p16, p21, and phosphorylated NFκB. PC treatment lowered intracellular ROS levels, increased ATP production, and promoted autophagy via LC3B-II accumulation and p62 reduction. In skin-derived precursor cells (SKPs), as well as mesenchymal stem cells (MSCs), PC treatment improved spheroid formation and growth while preserving the expression of key stemness markers, including Sox2, Oct4, and Nestin. Furthermore, PC exhibited antioxidant capacity (TEAC assay) and inhibited elastase, supporting its anti-aging potential. These findings suggest that PC is safe at concentrations below 1% and may serve as an effective natural compound to restore cellular homeostasis, reduce senescence and inflammation, and support stem cell health during aging.

## Linked entities

- **Genes:** CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029], CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], GTF2H1 (general transcription factor IIH subunit 1) [NCBI Gene 2965], SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657], POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460], nes.L (nestin L homeolog) [NCBI Gene 108699393]
- **Chemicals:** ATP (PubChem CID 5957)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460] {aka OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, NUP62 (nucleoporin 62) [NCBI Gene 23636] {aka IBSN, SNDI, p62}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** Inflammatory (MESH:D007249)
- **Chemicals:** Argan Callus (-), ATP (MESH:D000255), PC (MESH:C053518)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12291937/full.md

## References

97 references — full list in the complete paper: https://tomesphere.com/paper/PMC12291937/full.md

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Source: https://tomesphere.com/paper/PMC12291937