Argon plasma surface modification promotes the therapeutic angiogenesis and tissue formation of tissue-engineered scaffolds in vivo by adipose-derived stem cells.


Journal

Stem cell research & therapy
ISSN: 1757-6512
Titre abrégé: Stem Cell Res Ther
Pays: England
ID NLM: 101527581

Informations de publication

Date de publication:
29 03 2019
Historique:
received: 19 11 2018
accepted: 25 02 2019
revised: 21 02 2019
entrez: 30 3 2019
pubmed: 30 3 2019
medline: 26 6 2020
Statut: epublish

Résumé

Synthetic implants are being used to restore injured or damaged tissues following cancer resection and congenital diseases. However, the survival of large tissue implant replacements depends on their ability to support angiogenesis that if limited, causes extrusion and infection of the implant. This study assessed the beneficial effect of platelet-rich plasma (PRP) and adipose-derived stem cells (ADSCs) on synthetic biomaterials in combination with argon plasma surface modification to enhance vascularisation of tissue-engineered constructs. Non-biodegradable polyurethane scaffolds were manufactured and modified with plasma surface modification using argon gas (PM). Donor rats were then used to extract ADSCs and PRP to modify the scaffolds further. Scaffolds with and without PM were modified with and without ADSCs and PRP and subcutaneously implanted in the dorsum of rats for 3 months. After 12 weeks, the scaffolds were excised and the degree of tissue integration using H&E staining and Masson's trichrome staining, angiogenesis by CD31 and immune response by CD45 and CD68 immunohistochemistry staining was examined. H&E and Masson's trichrome staining showed PM+PRP+ADSC and PM+ADSC scaffolds had the greatest tissue integration, but there was no significant difference between the two scaffolds (p < 0.05). The greatest vessel formation after 3 months was shown with PM+PRP+ADSC and PM+ADSC scaffolds using CD31 staining compared to all other scaffolds (p < 0.05). The CD45 and CD68 staining was similar between all scaffolds after 3 months showing the ADSCs or PRP had no effect on the immune response of the scaffolds. Argon plasma surface modification enhanced the effect of adipose-derived stem cells effect on angiogenesis and tissue integration of polyurethane scaffolds. The combination of ADSCs and argon plasma modification may improve the survival of large tissue implants for regenerative applications.

Sections du résumé

BACKGROUND
Synthetic implants are being used to restore injured or damaged tissues following cancer resection and congenital diseases. However, the survival of large tissue implant replacements depends on their ability to support angiogenesis that if limited, causes extrusion and infection of the implant. This study assessed the beneficial effect of platelet-rich plasma (PRP) and adipose-derived stem cells (ADSCs) on synthetic biomaterials in combination with argon plasma surface modification to enhance vascularisation of tissue-engineered constructs.
METHODS
Non-biodegradable polyurethane scaffolds were manufactured and modified with plasma surface modification using argon gas (PM). Donor rats were then used to extract ADSCs and PRP to modify the scaffolds further. Scaffolds with and without PM were modified with and without ADSCs and PRP and subcutaneously implanted in the dorsum of rats for 3 months. After 12 weeks, the scaffolds were excised and the degree of tissue integration using H&E staining and Masson's trichrome staining, angiogenesis by CD31 and immune response by CD45 and CD68 immunohistochemistry staining was examined.
RESULTS
H&E and Masson's trichrome staining showed PM+PRP+ADSC and PM+ADSC scaffolds had the greatest tissue integration, but there was no significant difference between the two scaffolds (p < 0.05). The greatest vessel formation after 3 months was shown with PM+PRP+ADSC and PM+ADSC scaffolds using CD31 staining compared to all other scaffolds (p < 0.05). The CD45 and CD68 staining was similar between all scaffolds after 3 months showing the ADSCs or PRP had no effect on the immune response of the scaffolds.
CONCLUSIONS
Argon plasma surface modification enhanced the effect of adipose-derived stem cells effect on angiogenesis and tissue integration of polyurethane scaffolds. The combination of ADSCs and argon plasma modification may improve the survival of large tissue implants for regenerative applications.

Identifiants

pubmed: 30922398
doi: 10.1186/s13287-019-1195-z
pii: 10.1186/s13287-019-1195-z
pmc: PMC6440049
doi:

Substances chimiques

Plasma Gases 0
Argon 67XQY1V3KH

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

110

Subventions

Organisme : Medical Research Council
ID : GN2339
Pays : United Kingdom

Références

J Plast Reconstr Aesthet Surg. 2014 Dec;67(12):1726-34
pubmed: 25282633
J Biomed Mater Res B Appl Biomater. 2013 Jan;101(1):36-42
pubmed: 23161557
Ann Rheum Dis. 2015 Dec;74(12):2175-82
pubmed: 25114060
Int J Radiat Oncol Biol Phys. 2010 Nov 1;78(3):888-96
pubmed: 20708345
Plast Reconstr Surg. 2016 Mar;137(3):554e-565e
pubmed: 26910700
Mater Sci Eng C Mater Biol Appl. 2014 Jul 1;40:180-8
pubmed: 24857481
Trends Biotechnol. 2016 Jun;34(6):470-482
pubmed: 27138899
Tissue Eng Part C Methods. 2012 Mar;18(3):176-85
pubmed: 21951067
J Control Release. 2017 Nov 28;266:57-74
pubmed: 28935595
Plast Reconstr Surg. 2015 Jun;135(6):981e-989e
pubmed: 26017614
Tissue Eng Part A. 2015 May;21(9-10):1579-86
pubmed: 25625433
Biophys Rev. 2017 Dec;9(6):895-917
pubmed: 28971326
Stem Cell Rev Rep. 2014 Oct;10(5):671-85
pubmed: 24913279
Cochrane Database Syst Rev. 2016 May 25;(5):CD006899
pubmed: 27223580
Acta Biomater. 2016 Oct 1;43:3-13
pubmed: 27395828
Histopathology. 2010 Dec;57(6):796-805
pubmed: 21166694
Ann Plast Surg. 2015 May;74(5):615-20
pubmed: 25710554
Arthroscopy. 2018 Feb;34(2):581-591
pubmed: 29100775
Plast Reconstr Surg. 2016 Aug;138(2):397-408
pubmed: 27064225
Stem Cell Res Ther. 2015 Nov 05;6:215
pubmed: 26541973
Biomaterials. 2014 Nov;35(33):9033-40
pubmed: 25106769
J Biomed Mater Res A. 2015 Apr;103(4):1312-24
pubmed: 24890626
Burns. 2010 Dec;36(8):1222-7
pubmed: 20510519
J Plast Surg Hand Surg. 2012 Apr;46(2):59-68
pubmed: 22471250
Tissue Eng Part A. 2015 Mar;21(5-6):895-905
pubmed: 25287591
Stem Cells. 2016 Mar;34(3):668-73
pubmed: 26661694
Cytotherapy. 2014 Aug;16(8):1092-7
pubmed: 24726656
Cartilage. 2013 Oct;4(4):295-312
pubmed: 26069674
Biointerphases. 2013 Dec;8(1):23
pubmed: 24706135
J Transl Med. 2014 Jan 07;12:8
pubmed: 24397850
J Burn Care Res. 2010 Jan-Feb;31(1):158-75
pubmed: 20061852
Exp Ther Med. 2016 Mar;11(3):737-746
pubmed: 26997987
Semin Immunol. 2008 Apr;20(2):86-100
pubmed: 18162407
Circ Res. 2007 May 11;100(9):1249-60
pubmed: 17495232
Biomaterials. 2012 May;33(15):3792-802
pubmed: 22386919
Int J Nanomedicine. 2018 Oct 08;13:6123-6141
pubmed: 30349241
BMC Musculoskelet Disord. 2013 Dec 01;14:337
pubmed: 24289766
Acta Biomater. 2017 Mar 1;50:450-461
pubmed: 27956359
Singapore Med J. 2017 Sep;58(9):551-556
pubmed: 27193079
Arthroscopy. 2013 Apr;29(4):748-55
pubmed: 23375182
Rheumatology (Oxford). 2016 Feb;55(2):301-6
pubmed: 26350489
Int Endod J. 2012 Sep;45(9):859-64
pubmed: 22486765
Arch Dermatol Res. 2016 Sep;308(7):511-20
pubmed: 27394438
Clin Hemorheol Microcirc. 2016;61(4):599-614
pubmed: 25536920
Cell Transplant. 2013;22(3):437-45
pubmed: 23031161
Biomater Sci. 2016 Jan;4(1):145-58
pubmed: 26474453
J Surg Res. 2015 Dec;199(2):412-9
pubmed: 26182999
J Plast Surg Hand Surg. 2013 Jun;47(3):169-74
pubmed: 23621096

Auteurs

M F Griffin (MF)

UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, UK. 12michellegriffin@gmail.com.
Royal Free London NHS Foundation Trust Hospital, London, UK. 12michellegriffin@gmail.com.
Charles Wolfson Center for Reconstructive Surgery, Royal Free Hospital, London, UK. 12michellegriffin@gmail.com.
Plastic and Reconstructive Surgery Department, Royal Free Hospital, University College London, Pond Street, London, UK. 12michellegriffin@gmail.com.

N Naderi (N)

UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, UK.
Royal Free London NHS Foundation Trust Hospital, London, UK.

D M Kalaskar (DM)

UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, UK.
UCL Institute of Orthopaedics and Musculoskeletal Science, Division of Surgery and Interventional Science, University College London, Stanmore, Middlesex, HA7 4LP, UK.

A M Seifalian (AM)

Nanotechnology and Regenerative Medicine Commercialization Centre (Ltd), The London Bioscience Innovation Centre, London, NW1 0NH, UK.

P E Butler (PE)

UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, UK.
Royal Free London NHS Foundation Trust Hospital, London, UK.
Charles Wolfson Center for Reconstructive Surgery, Royal Free Hospital, London, UK.

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