Comprehensive Characterization of Tissues Derived from Animals at Different Regenerative Stages: A Comparative Analysis between Fetal and Adult Mouse Skin

Cells. 2023 Apr 22;12(9):1215. doi: 10.3390/cells12091215.

Abstract

Tissue regeneration capabilities vary significantly throughout an organism's lifespan. For example, mammals can fully regenerate until they reach specific developmental stages, after which they can only repair the tissue without restoring its original architecture and function. The high regenerative potential of fetal stages has been attributed to various factors, such as stem cells, the immune system, specific growth factors, and the presence of extracellular matrix molecules upon damage. To better understand the local differences between regenerative and reparative tissues, we conducted a comparative analysis of skin derived from mice at regenerative and reparative stages. Our findings show that both types of skin differ in their molecular composition, structure, and functionality. We observed a significant increase in cellular density, nucleic acid content, neutral lipid density, Collagen III, and glycosaminoglycans in regenerative skin compared with reparative skin. Additionally, regenerative skin had significantly higher porosity, metabolic activity, water absorption capacity, and elasticity than reparative skin. Finally, our results also revealed significant differences in lipid distribution, extracellular matrix pore size, and proteoglycans between the two groups. This study provides comprehensive data on the molecular and structural clues that enable full tissue regeneration in fetal stages, which could aid in developing new biomaterials and strategies for tissue engineering and regeneration.

Keywords: extracellular matrix; skin; tissue regeneration; tissue repair.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials
  • Collagen*
  • Lipids
  • Mammals
  • Mice
  • Wound Healing*

Substances

  • Collagen
  • Biocompatible Materials
  • Lipids

Grants and funding

This research was supported by the Chilean Agencia Nacional de Investigación y Desarrollo (ANID) through the projects FONDECYT Nr. 1200280 (to J.T.E.), Beca Doctorado Nacional Nr. 21180336/2018 (to V.C.), and Beca Magíster Nacional Nr. 5301/2019 (to P.D.-A.).