Distinct origin and region-dependent contribution of stromal fibroblasts to fibrosis following traumatic injury in mice.
Daniel HollWing Fung HauAnais JulienShervin BanitalebiJannis KalkitsasSoniya SavantEnric Llorens-BobadillaYann HéraultGuillaume PavlovicMahmood Amiry-MoghaddamDavid Oliveira DiasChristian GöritzPublished in: Nature neuroscience (2024)
Fibrotic scar tissue formation occurs in humans and mice. The fibrotic scar impairs tissue regeneration and functional recovery. However, the origin of scar-forming fibroblasts is unclear. Here, we show that stromal fibroblasts forming the fibrotic scar derive from two populations of perivascular cells after spinal cord injury (SCI) in adult mice of both sexes. We anatomically and transcriptionally identify the two cell populations as pericytes and perivascular fibroblasts. Fibroblasts and pericytes are enriched in the white and gray matter regions of the spinal cord, respectively. Both cell populations are recruited in response to SCI and inflammation. However, their contribution to fibrotic scar tissue depends on the location of the lesion. Upon injury, pericytes and perivascular fibroblasts become activated and transcriptionally converge on the generation of stromal myofibroblasts. Our results show that pericytes and perivascular fibroblasts contribute to the fibrotic scar in a region-dependent manner.
Keyphrases
- extracellular matrix
- spinal cord injury
- systemic sclerosis
- wound healing
- spinal cord
- idiopathic pulmonary fibrosis
- bone marrow
- high fat diet induced
- single cell
- cell therapy
- induced apoptosis
- type diabetes
- insulin resistance
- skeletal muscle
- neuropathic pain
- young adults
- adipose tissue
- cell cycle arrest
- endoplasmic reticulum stress
- cell proliferation
- cell death