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Series GSE168748 Query DataSets for GSE168748
Status Public on Dec 08, 2022
Title Skin regeneration is enabled in the absence of fibroblast inflammatory priming
Organism Rangifer tarandus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.

Project abstract: In adult mammals, skin wound healing has evolved to favor rapid repair through the formation of fibrotic scar. These dermal scars are dysfunctional and may lead to chronic disfigurement and disability, yet the biologic mechanisms that drive fibrosis and prevent tissue regeneration remain unknown. Here, we report that reindeer (Rangifer tarandus) antler velvet exhibits regenerative wound healing, whereas identical full-thickness injury in dorsal back skin of the same animal forms fibrotic scar. This regenerative capacity is retained even following ectopic transplantation of velvet to a scar-forming site, demonstrating that this latent regenerative capacity is innate to velvet cells and independent of local factors derived from the growing antler. Single cell RNA-sequencing of uninjured skin revealed a marked divergence in resting fibroblast transcriptional states and immunomodulatory function. Uninjured velvet fibroblast shared a striking resemblance with human fetal fibroblasts whereas uninjured back skin fibroblasts exhibited an overrepresentation of pro-inflammatory genes resembling adult human fibroblasts. Identical skin injury resulted in site-specific fibroblast polarization; back fibroblasts exacerbated the inflammatory response, whereas velvet fibroblasts adopted an immunosuppressive state and reverted back to a regeneration-competent ground state. Consequently, velvet wounds exhibited an accelerated adoption of anti-inflammatory immune states and an expedited resolution of immune response. This study demonstrates reindeer as a novel comparative mammalian model to study both adult skin regeneration (velvet) and scar formation (back skin) within the same animal. Our study underscores the importance of fibroblast heterogeneity in shaping local immune cell functions that ultimately polarize wound healing outcomes. Purposeful, acute modulation of fibroblast-mediated immune signaling represents an important therapeutic avenue to mitigate scar and improve wound healing.
 
Overall design Refer to individual Series
 
Citation(s) 36493752
Submission date Mar 11, 2021
Last update date Feb 02, 2023
Contact name Jeff Biernaskie
E-mail(s) jabierna@ucalgary.ca
Phone 4032107306
Organization name University of Calgary
Department Comparative Biology and Experimental Medicine
Lab Biernaskie Lab
Street address 3330 Hospital Drive NW
City Calgary
State/province Alberta
ZIP/Postal code T2N4N1
Country Canada
 
Platforms (2)
GPL27966 Illumina NovaSeq 6000 (Rangifer tarandus)
GPL29839 Illumina HiSeq 3000 (Rangifer tarandus)
Samples (61)
GSM4244978 scRNA-Seq_Day0_Antler
GSM4244979 scRNA-Seq_Day0_Back_RNA
GSM4244980 scRNA-Seq_Day3_Antler_RNA
This SuperSeries is composed of the following SubSeries:
GSE142854 Single-cell RNA-Seq datasets supporting fibroblast polarization drives skin regeneration versus fibrosis in adult reindeer
GSE153095 Single-cell profiling of ectopic velvet grafts transplanted onto non-regenerative backskin to assess whether regenerative propensity is intrinsic to reindeer velvet
GSE168746 Bulk RNA-Seq datasets supporting fibroblast polarization drives skin regeneration versus fibrosis in adult reindeer
Relations
BioProject PRJNA713822

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE168748_RAW.tar 1.2 Gb (http)(custom) TAR (of BED, H5, MTX, TSV)
SRA Run SelectorHelp

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