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Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds

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Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds. / Mills, S. J.; Kirby, G. T.; Hofma, B. R. et al.
In: Frontiers in Bioengineering and Biotechnology, Vol. 11, 22.08.2023.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Mills, SJ, Kirby, GT, Hofma, BR, Smith, LE, Statham, P, Vaes, B, Ting, AE, Short, R & Cowin, AJ 2023, 'Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds', Frontiers in Bioengineering and Biotechnology, vol. 11. https://doi.org/10.3389/fbioe.2023.1213021

APA

Mills, S. J., Kirby, G. T., Hofma, B. R., Smith, L. E., Statham, P., Vaes, B., Ting, A. E., Short, R., & Cowin, A. J. (2023). Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds. Frontiers in Bioengineering and Biotechnology, 11. https://doi.org/10.3389/fbioe.2023.1213021

Vancouver

Mills SJ, Kirby GT, Hofma BR, Smith LE, Statham P, Vaes B et al. Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds. Frontiers in Bioengineering and Biotechnology. 2023 Aug 22;11. doi: 10.3389/fbioe.2023.1213021

Author

Mills, S. J. ; Kirby, G. T. ; Hofma, B. R. et al. / Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds. In: Frontiers in Bioengineering and Biotechnology. 2023 ; Vol. 11.

Bibtex

@article{124004245b2f4bbb89be31097f13f1e0,
title = "Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds",
abstract = "Introduction: Stem cell therapies have been investigated as potential treatment modalities for chronic wounds however there has been limited success to date. Multipotent Adult Progenitor Cells (MAPCs{\textcopyright}) have been identified as having potential as an allogenic stem cell product due to their high population doubling number and their characteristic dampening of T-cell proliferation. This helps to prevent autoimmunity and graft/cell rejection. Methods: We have developed a dressing, consisting of medical grade silicone coated with a heptylamine plasma polymer, which supports the growth and transfer of MAPCs to skin. To determine if the dressing can deliver functional stem cells into diabetic wounds, they were loaded with MAPCs and then placed over excisional wounds in both normal and diabetic mice. Results and discussion: Accelerated healing was observed in both the normal and diabetic wounds with wound gape being significantly smaller at day 3 when compared to controls. Wound analysis showed that treatment with the MAPC dressings dampened the inflammatory response with reduced numbers of neutrophils and macrophages observed. Additionally, an increase in pro-angiogenic VEGF and CD31 positive endothelial cells was observed indicating improved new blood vessel formation. The MAPC dressings had no effect on fibrosis with collagen I and III being equally affected in both control and treated wounds. Overall, the functionalized MAPC dressings improve healing responses particularly in diabetic mice with impaired healing responses and therefore, show potential for development as an advanced therapeutic approach for the treatment of chronic diabetic wounds.",
keywords = "diabetes, plasma polymerization, wounds, biomaterials, Inflammation, MAPC",
author = "Mills, {S. J.} and Kirby, {G. T.} and Hofma, {B. R.} and Smith, {L. E.} and P. Statham and B. Vaes and Ting, {A. E.} and R. Short and Cowin, {A. J.}",
year = "2023",
month = aug,
day = "22",
doi = "10.3389/fbioe.2023.1213021",
language = "English",
volume = "11",
journal = "Frontiers in Bioengineering and Biotechnology",
issn = "2296-4185",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Delivery of multipotent adult progenitor cells via a functionalized plasma polymerized surface accelerates healing of murine diabetic wounds

AU - Mills, S. J.

AU - Kirby, G. T.

AU - Hofma, B. R.

AU - Smith, L. E.

AU - Statham, P.

AU - Vaes, B.

AU - Ting, A. E.

AU - Short, R.

AU - Cowin, A. J.

PY - 2023/8/22

Y1 - 2023/8/22

N2 - Introduction: Stem cell therapies have been investigated as potential treatment modalities for chronic wounds however there has been limited success to date. Multipotent Adult Progenitor Cells (MAPCs©) have been identified as having potential as an allogenic stem cell product due to their high population doubling number and their characteristic dampening of T-cell proliferation. This helps to prevent autoimmunity and graft/cell rejection. Methods: We have developed a dressing, consisting of medical grade silicone coated with a heptylamine plasma polymer, which supports the growth and transfer of MAPCs to skin. To determine if the dressing can deliver functional stem cells into diabetic wounds, they were loaded with MAPCs and then placed over excisional wounds in both normal and diabetic mice. Results and discussion: Accelerated healing was observed in both the normal and diabetic wounds with wound gape being significantly smaller at day 3 when compared to controls. Wound analysis showed that treatment with the MAPC dressings dampened the inflammatory response with reduced numbers of neutrophils and macrophages observed. Additionally, an increase in pro-angiogenic VEGF and CD31 positive endothelial cells was observed indicating improved new blood vessel formation. The MAPC dressings had no effect on fibrosis with collagen I and III being equally affected in both control and treated wounds. Overall, the functionalized MAPC dressings improve healing responses particularly in diabetic mice with impaired healing responses and therefore, show potential for development as an advanced therapeutic approach for the treatment of chronic diabetic wounds.

AB - Introduction: Stem cell therapies have been investigated as potential treatment modalities for chronic wounds however there has been limited success to date. Multipotent Adult Progenitor Cells (MAPCs©) have been identified as having potential as an allogenic stem cell product due to their high population doubling number and their characteristic dampening of T-cell proliferation. This helps to prevent autoimmunity and graft/cell rejection. Methods: We have developed a dressing, consisting of medical grade silicone coated with a heptylamine plasma polymer, which supports the growth and transfer of MAPCs to skin. To determine if the dressing can deliver functional stem cells into diabetic wounds, they were loaded with MAPCs and then placed over excisional wounds in both normal and diabetic mice. Results and discussion: Accelerated healing was observed in both the normal and diabetic wounds with wound gape being significantly smaller at day 3 when compared to controls. Wound analysis showed that treatment with the MAPC dressings dampened the inflammatory response with reduced numbers of neutrophils and macrophages observed. Additionally, an increase in pro-angiogenic VEGF and CD31 positive endothelial cells was observed indicating improved new blood vessel formation. The MAPC dressings had no effect on fibrosis with collagen I and III being equally affected in both control and treated wounds. Overall, the functionalized MAPC dressings improve healing responses particularly in diabetic mice with impaired healing responses and therefore, show potential for development as an advanced therapeutic approach for the treatment of chronic diabetic wounds.

KW - diabetes

KW - plasma polymerization

KW - wounds

KW - biomaterials

KW - Inflammation

KW - MAPC

U2 - 10.3389/fbioe.2023.1213021

DO - 10.3389/fbioe.2023.1213021

M3 - Journal article

VL - 11

JO - Frontiers in Bioengineering and Biotechnology

JF - Frontiers in Bioengineering and Biotechnology

SN - 2296-4185

ER -