TY - JOUR
T1 - Transcriptomic, Proteomic, and Morphologic Characterization of Healing in Volumetric Muscle Loss
AU - Crum, Raphael J.
AU - Johnson, Scott A.
AU - Jiang, Peng
AU - Jui, Jayati H.
AU - Zamora, Ruben
AU - Cortes, Devin
AU - Kulkarni, Mangesh
AU - Prabahar, Archana
AU - Bolin, Jennifer
AU - Gann, Eric
AU - Elster, Eric
AU - Schobel, Seth A.
AU - Larie, Dale
AU - Cockrell, Chase
AU - An, Gary
AU - Brown, Bryan
AU - Hauskrecht, Milos
AU - Vodovotz, Yoram
AU - Badylak, Stephen F.
N1 - Publisher Copyright:
© 2022 Mary Ann Liebert Inc.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Skeletal muscle has a robust, inherent ability to regenerate in response to injury from acute to chronic. In severe trauma, however, complete regeneration is not possible, resulting in a permanent loss of skeletal muscle tissue referred to as volumetric muscle loss (VML). There are few consistently reliable therapeutic or surgical options to address VML. A major limitation in investigation of possible therapies is the absence of a well-characterized large animal model. In this study, we present results of a comprehensive transcriptomic, proteomic, and morphologic characterization of wound healing following VML in a novel canine model of VML which we compare to a nine-patient cohort of combat-associated VML. The canine model is translationally relevant as it provides both a regional (spatial) and temporal map of the wound healing processes that occur in human VML. Collectively, these data show the spatiotemporal transcriptomic, proteomic, and morphologic properties of canine VML healing as a framework and model system applicable to future studies investigating novel therapies for human VML. The spatiotemporal transcriptomic, proteomic, and morphologic properties of canine volumetric muscle loss (VML) healing is a translational framework and model system applicable to future studies investigating novel therapies for human VML.
AB - Skeletal muscle has a robust, inherent ability to regenerate in response to injury from acute to chronic. In severe trauma, however, complete regeneration is not possible, resulting in a permanent loss of skeletal muscle tissue referred to as volumetric muscle loss (VML). There are few consistently reliable therapeutic or surgical options to address VML. A major limitation in investigation of possible therapies is the absence of a well-characterized large animal model. In this study, we present results of a comprehensive transcriptomic, proteomic, and morphologic characterization of wound healing following VML in a novel canine model of VML which we compare to a nine-patient cohort of combat-associated VML. The canine model is translationally relevant as it provides both a regional (spatial) and temporal map of the wound healing processes that occur in human VML. Collectively, these data show the spatiotemporal transcriptomic, proteomic, and morphologic properties of canine VML healing as a framework and model system applicable to future studies investigating novel therapies for human VML. The spatiotemporal transcriptomic, proteomic, and morphologic properties of canine volumetric muscle loss (VML) healing is a translational framework and model system applicable to future studies investigating novel therapies for human VML.
KW - regenerative medicine
KW - tissue engineering
KW - volumetric muscle loss
KW - wound healing
UR - http://www.scopus.com/inward/record.url?scp=85144587090&partnerID=8YFLogxK
U2 - 10.1089/ten.tea.2022.0113
DO - 10.1089/ten.tea.2022.0113
M3 - Article
C2 - 36039923
AN - SCOPUS:85144587090
SN - 1937-3341
VL - 28
SP - 941
EP - 957
JO - Tissue Engineering - Part A.
JF - Tissue Engineering - Part A.
IS - 23-24
ER -