Generation and characterization of two immortalized dermal fibroblast cell lines from the spiny mouse (Acomys).

PLoS One

J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida, United States of America.

Published: July 2023

AI Article Synopsis

  • The spiny mouse is special because it can heal its injuries really well without leaving scars.
  • Scientists want to study it to learn how to help humans heal better, but it’s hard to get enough of these mice for experiments.
  • To solve this problem, researchers created two types of immortal mouse cells that act like the real ones, making it easier to study and find new ways for humans to heal from wounds.

Article Abstract

The spiny mouse (Acomys) is gaining popularity as a research organism due to its phenomenal regenerative capabilities. Acomys recovers from injuries to several organs without fibrosis. For example, Acomys heals full thickness skin injuries with rapid re-epithelialization of the wound and regeneration of hair follicles, sebaceous glands, erector pili muscles, adipocytes, and dermis without scarring. Understanding mechanisms of Acomys regeneration may uncover potential therapeutics for wound healing in humans. However, access to Acomys colonies is limited and primary fibroblasts can only be maintained in culture for a limited time. To address these obstacles, we generated immortalized Acomys dermal fibroblast cell lines using two methods: transfection with the SV40 large T antigen and spontaneous immortalization. The two cell lines (AcoSV40 and AcoSI-1) maintained the morphological and functional characteristics of primary Acomys fibroblasts, including maintenance of key fibroblast markers and ECM deposition. The availability of these cells will lower the barrier to working with Acomys as a model research organism, increasing the pace at which new discoveries to promote regeneration in humans can be made.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328323PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0280169PLOS

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