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Renewal of Skin Epidermal Stem Cells01:12

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The skin is divided into epidermis, dermis, and hypodermis, the skin's outermost, middle, and inner layers. The human epidermal layer regularly undergoes renewal, where old, dead cells are replaced by new cells. Epidermal stem cells or EpiSCs divide and differentiate to restore the lost cells. For the renewal process, some EpiSCs continuously self-renew. In contrast, few others differentiate into transit-amplifying cells, which later form prickle or spinous cells, followed by granular...
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Related Experiment Video

Updated: Sep 10, 2025

Human Ex vivo Wound Model and Whole-Mount Staining Approach to Accurately Evaluate Skin Repair
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High-Resolution Spatial Transcriptomics Unveils Spatially Resolved Gene Modules and Fatty Acid Metabolism

Yin Li1, Wenwan Zhang1, Yao Teng2

  • 1Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.

The Journal of Investigative Dermatology
|August 24, 2025
PubMed
Summary

Human skin aging involves cellular changes, with reduced fatty acid synthesis contributing to senescence and barrier dysfunction. This study reveals new molecular mechanisms for skin aging interventions.

Keywords:
Human skinSkin agingSpatial transcriptomicsStereo-seq

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Area of Science:

  • Dermatology
  • Genomics
  • Molecular Biology

Background:

  • Human skin aging involves complex cellular and molecular changes.
  • High-resolution spatial transcriptomics is key to understanding these age-related alterations.

Purpose of the Study:

  • To create a high-resolution spatial transcriptomic atlas of human eyelid skin.
  • To identify molecular mechanisms driving skin aging and potential intervention targets.

Main Methods:

  • Stereo-seq for spatial transcriptomic analysis.
  • Multiplexed fluorescent in situ hybridization (FISH) for spatial mapping.
  • Functional studies using keratinocytes and a T-Skin model.

Main Results:

  • Identified 8 spatial tissue clusters and 18 gene modules in aging skin.
  • Revealed decreased dermal-epidermal communication, reduced fatty acid synthesis, and epidermal cell identity loss.
  • Showed reduced FDPS and FASN activity promotes epidermal senescence and barrier dysfunction.

Conclusions:

  • Spatially resolved transcriptomics offers novel insights into skin aging mechanisms.
  • Reduced fatty acid synthesis is a key driver of age-related skin deterioration.
  • Findings suggest new targets for anti-aging interventions.