MicroRNA-29a Exhibited Pro-Angiogenic and Anti-Fibrotic Features to Intensify Human Umbilical Cord Mesenchymal Stem Cells-Renovated Perfusion Recovery and Preventing against Fibrosis from Skeletal Muscle Ischemic Injury
This study was conducted to elucidate whether ( ) and/or together with transplantation of mesenchymal stem cells isolated from umbilical cord Wharton's jelly (uMSCs) could aid in skeletal muscle healing and putative molecular mechanisms. We established a skeletal muscle ischemic injury model by...
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Veröffentlicht in: | International journal of molecular sciences 2019-11, Vol.20 (23), p.5859 |
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Sprache: | eng |
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Zusammenfassung: | This study was conducted to elucidate whether
(
) and/or together with transplantation of mesenchymal stem cells isolated from umbilical cord Wharton's jelly (uMSCs) could aid in skeletal muscle healing and putative molecular mechanisms. We established a skeletal muscle ischemic injury model by injection of a myotoxin bupivacaine (BPVC) into gastrocnemius muscle of C57BL/6 mice. Throughout the angiogenic and fibrotic phases of muscle healing,
was considerably downregulated in BPVC-injured gastrocnemius muscle. Overexpressed
efficaciously promoted human umbilical vein endothelial cells proliferation and capillary-like tube formation in vitro, crucial steps for neoangiogenesis, whereas knockdown of
notably suppressed those endothelial functions. Remarkably, overexpressed
profitably elicited limbic flow perfusion and estimated by Laser Dopple.
motivated perfusion recovery through abolishing the tissue inhibitor of metalloproteinase (TIMP)-2, led great numbers of pro-angiogenic matrix metalloproteinases (MMPs) to be liberated from bondage of TIMP, thus reinforced vascular development. Furthermore, engrafted uMSCs also illustrated comparable effect to restore the flow perfusion and augmented vascular endothelial growth factors-A, -B, and -C expression. Notably, the combination of
and the uMSCs treatments revealed the utmost renovation of limbic flow perfusion. Amplified
also adequately diminished the collagen deposition and suppressed broad-wide
targeted extracellular matrix components expression. Consistently,
administration intensified the relevance of uMSCs to abridge BPVC-aggravated fibrosis. Our data support that
is a promising pro-angiogenic and anti-fibrotic
which delivers numerous advantages to endorse angiogenesis, perfusion recovery, and protect against fibrosis post injury. Amalgamation of nucleic acid-based strategy (
) together with the stem cell-based strategy (uMSCs) may be an innovative and eminent strategy to accelerate the healing process post skeletal muscle injury. |
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ISSN: | 1422-0067 1661-6596 1422-0067 |
DOI: | 10.3390/ijms20235859 |