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Status |
Public on Sep 16, 2020 |
Title |
Deregulated immune signature orchestrated by FOXM1 impairs human diabetic wound healing |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We performed RNA-seq on tissue biopsies derived from patients with DFUs and compared it to human oral and skin wounds to identify the molecular mechanisms and transcriptional networks that are deregulated in DFUs. Our results identified a unique inflammatory transcriptional signature unique to oral and skin wounds involved in promoting cell proliferation and cell survival of immune cells that are deficient in DFUs. In addition, we identified a signature immune-cell profile in which activation and proliferation of macrophages and neutrophils were absent in DFUs. These results suggest that a deregulated immune response in which impaired activation, proliferation and survival of immune cells contribute to pathogenesis of DFUs and provides novel avenues for development of therapies aimed at reprogramming DFUs into healing-competent wounds.
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Overall design |
Transcriptome profiles from patients with diabetic foot ulcers generated by deep sequencing using Illumina NextSeq500.
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Contributor(s) |
Morasso M, Tomic-Canic M, Brooks SR |
Citation(s) |
32938916 |
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Submission date |
Jul 17, 2019 |
Last update date |
Oct 06, 2020 |
Contact name |
Stephen R Brooks |
E-mail(s) |
stephen.brooks@nih.gov
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Organization name |
NIAMS/NIH
|
Department |
Biodata Mining and Discovery Section
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Street address |
50 SOUTH DR, RM 1140
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20814 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (21)
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Relations |
BioProject |
PRJNA555081 |
SRA |
SRP215049 |