Matrisomal components involved in regenerative wound healing in axolotl and Acomys : implications for biomaterial development.
Nancy Avila-MartinezMerel GansevoortJuul VerbakelHaarshaadri JayaprakashInês Maria AraújoMarta VitorinoGustavo TiscorniaToin H van KuppeveltWilleke F DaamenPublished in: Biomaterials science (2023)
Achieving regeneration in humans has been a long-standing goal of many researchers. Whereas amphibians like the axolotl ( Ambystoma mexicanum ) are capable of regenerating whole organs and even limbs, most mammals heal their wounds via fibrotic scarring. Recently, the African spiny mouse ( Acomys sp.) has been shown to be injury resistant and capable of regenerating several tissue types. A major focal point of research with Acomys has been the identification of drivers of regeneration. In this search, the matrisome components related to the extracellular matrix (ECM) are often overlooked. In this review, we compare Acomys and axolotl skin wound healing and blastema-mediated regeneration by examining their wound healing responses and comparing the expression pattern of matrisome genes, including glycosaminoglycan (GAG) related genes. The goal of this review is to identify matrisome genes that are upregulated during regeneration and could be potential candidates for inclusion in pro-regenerative biomaterials. Research papers describing transcriptomic or proteomic coverage of either skin regeneration or blastema formation in Acomys and axolotl were selected. Matrisome and GAG related genes were extracted from each dataset and the resulting lists of genes were compared. In our analysis, we found several genes that were consistently upregulated, suggesting possible involvement in regenerative processes. Most of the components have been implicated in regulation of cell behavior, extracellular matrix remodeling and wound healing. Incorporation of such pro-regenerative factors into biomaterials may help to shift pro-fibrotic processes to regenerative responses in treated wounds.
Keyphrases
- wound healing
- extracellular matrix
- stem cells
- tissue engineering
- cell therapy
- mesenchymal stem cells
- bioinformatics analysis
- genome wide
- genome wide identification
- anti inflammatory
- single cell
- poor prognosis
- genome wide analysis
- systemic sclerosis
- gene expression
- healthcare
- transcription factor
- risk assessment
- bone marrow
- bone regeneration
- drug induced
- climate change
- binding protein
- label free
- soft tissue