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The role of indoleamine 2,3 dioxygenase in beneficial effects of stem cells in hind limb ischemia reperfusion injury

Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Ischemia-Reperfusion (IR) injury of limb remains a significant clinical problem causing secondary complications and restricting clinical recovery, despite rapid restoration of blood flow and successful surgery. In an attempt to further improve post ischemic tissue repair, we investigated the effect of a local administration of bone marrow derived stem cells (BMDSCs) in the presence or absence of immune-regulatory enzyme, IDO, in a murine model. A whole limb warm ischemia-reperfusion model was developed using IDO sufficient (WT) and deficient (KO) mice with C57/BL6 background. Twenty-four hours after injury, 5x105 cells (5x105 cells/200 μL of PBS solution) BMDSCs (Sca1 + cells) were injected intramuscularly while the control group received just the vehicle buffer (PBS). Forty-eight to seventy-two hours after limb BMDSC injection, recovery status including the ratio of intrinsic paw function between affected and normal paws, general mobility, and inflammatory responses were measured using video micrometery, flow cytometry, and immunohistochemistry techniques. Additionally, MRI/MRA studies were performed to further study the inflammatory response between groups and to confirm reconstitution of blood flow after ischemia. For the first time, our data, showed that IDO may potentially represent a partial role in triggering the beneficial effects of BMDSCs in faster recovery and protection against structural changes and cellular damage in a hind limb IR injury setting (P = 0.00058).

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e95720

Journal (Volume, Issue Number)

PloS one (Volume 9, Issue 4)

Publication milestones

  • Published - 04/21/2014

Publication status

Published - 04/21/2014

ISSN

1932-6203

Publication IDs

  • Scopus: 84899704798
  • PubMed: 24752324

Publication metrics

Metrics

Scopus
citations
SciVal
citations
6
SciVal
FWCI
0.37
SciVal
Author count
8
SciVal
Paper percentile
57
Fractional count
5
Fractional count
0.63
Fractional count
3
Fractional count
0.38
Fractional count
5
Fractional count
1

PlumX, opens in new tab

Captures
26
Citation count
7

Funding Details

This study was supported by institutional funds (provided to BB) and the Milford B. Hatcher Endowment (provided to JY). The authors are grateful to Mrs. Michelle Barnes for her administrative support.
FunderFunding numbers
Milford B. Hatcher Endowment
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