Photodynamic therapy accelerates skin wound healing through promoting re-epithelialization.
5-aminolevulinic acid
Epidermal stem cells
Photodynamic therapy
Re-epithelialization
Transient amplifying cells
Wound healing
Journal
Burns & trauma
ISSN: 2321-3868
Titre abrégé: Burns Trauma
Pays: England
ID NLM: 101651457
Informations de publication
Date de publication:
2021
2021
Historique:
received:
17
12
2020
revised:
01
02
2021
entrez:
13
9
2021
pubmed:
14
9
2021
medline:
14
9
2021
Statut:
epublish
Résumé
Epidermal stem cells (EpSCs) that reside in cutaneous hair follicles and the basal layer of the epidermis are indispensable for wound healing and skin homeostasis. Little is known about the effects of photochemical activation on EpSC differentiation, proliferation and migration during wound healing. The present study aimed to determine the effects of photodynamic therapy (PDT) on wound healing We created mouse full-thickness skin resection models and applied 5-aminolevulinic acid (ALA) for PDT to the wound beds. Wound healing was analysed by gross evaluation and haematoxylin-eosin staining PDT accelerated wound closure by enhancing EpSC differentiation, proliferation and migration, thereby promoting re-epithelialization and angiogenesis. PDT inhibited inflammatory infiltration and expression of proinflammatory cytokines, whereas the secretion of growth factors was greater than in other groups. The proportion of transient amplifying cells was significantly greater Topical ALA-induced PDT stimulates wound healing by enhancing re-epithelialization, promoting angiogenesis as well as modulating skin homeostasis. This work provides a preliminary theoretical foundation for the clinical administration of topical ALA-induced PDT in skin wound healing.
Sections du résumé
BACKGROUND
BACKGROUND
Epidermal stem cells (EpSCs) that reside in cutaneous hair follicles and the basal layer of the epidermis are indispensable for wound healing and skin homeostasis. Little is known about the effects of photochemical activation on EpSC differentiation, proliferation and migration during wound healing. The present study aimed to determine the effects of photodynamic therapy (PDT) on wound healing
METHODS
METHODS
We created mouse full-thickness skin resection models and applied 5-aminolevulinic acid (ALA) for PDT to the wound beds. Wound healing was analysed by gross evaluation and haematoxylin-eosin staining
RESULTS
RESULTS
PDT accelerated wound closure by enhancing EpSC differentiation, proliferation and migration, thereby promoting re-epithelialization and angiogenesis. PDT inhibited inflammatory infiltration and expression of proinflammatory cytokines, whereas the secretion of growth factors was greater than in other groups. The proportion of transient amplifying cells was significantly greater
CONCLUSIONS
CONCLUSIONS
Topical ALA-induced PDT stimulates wound healing by enhancing re-epithelialization, promoting angiogenesis as well as modulating skin homeostasis. This work provides a preliminary theoretical foundation for the clinical administration of topical ALA-induced PDT in skin wound healing.
Identifiants
pubmed: 34514005
doi: 10.1093/burnst/tkab008
pii: tkab008
pmc: PMC8420953
doi:
Types de publication
Journal Article
Langues
eng
Pagination
tkab008Informations de copyright
© The Author(s) 2021. Published by Oxford University Press.
Références
Adv Wound Care (New Rochelle). 2020 Apr 1;9(4):161-173
pubmed: 32117580
Burns Trauma. 2019 Aug 13;7:19
pubmed: 31413962
Nat Med. 2014 Aug;20(8):847-56
pubmed: 25100530
FASEB J. 2007 May;21(7):1358-66
pubmed: 17255473
Cold Spring Harb Perspect Med. 2014 Jul 03;4(10):
pubmed: 24993676
Burns Trauma. 2020 Aug 14;8:tkaa028
pubmed: 32821743
Cell Stem Cell. 2011 Jan 7;8(1):59-71
pubmed: 21211782
Lasers Med Sci. 2010 Mar;25(2):221-8
pubmed: 19533211
Nat Rev Mol Cell Biol. 2014 Jun;15(6):411-21
pubmed: 24854789
Mil Med Res. 2020 Apr 22;7(1):20
pubmed: 32321591
Eur J Cell Biol. 2012 Mar;91(3):216-23
pubmed: 22293959
Methods Mol Biol. 2019;1879:101-110
pubmed: 29980942
Front Physiol. 2017 Dec 06;8:1004
pubmed: 29270129
Mil Med Res. 2019 Jul 23;6(1):22
pubmed: 31331385
Vet Dermatol. 2015 Aug;26(4):213-e47
pubmed: 25963063
Front Immunol. 2018 Feb 12;9:240
pubmed: 29483920
Wound Repair Regen. 2015 Sep;23(5):685-702
pubmed: 26094764
J Invest Dermatol. 2009 Feb;129(2):480-90
pubmed: 18719609
Acta Biomater. 2016 Jan;30:246-257
pubmed: 26602823
Nature. 2008 May 15;453(7193):314-21
pubmed: 18480812
Chem Rev. 2010 May 12;110(5):2795-838
pubmed: 20353192
J Invest Dermatol. 2015 Nov;135(11):2611-2622
pubmed: 26134949
Sci Rep. 2016 Jan 13;6:19395
pubmed: 26759072
J Biophotonics. 2018 Jun;11(6):e201700357
pubmed: 29431281
Biomaterials. 2015 Feb;40:1-11
pubmed: 25498800
Lasers Med Sci. 2009 Mar;24(2):259-68
pubmed: 18247081
J Invest Dermatol. 2000 Mar;114(3):413-20
pubmed: 10692098
Adv Wound Care (New Rochelle). 2013 Jul;2(6):273-282
pubmed: 24527349
J Invest Dermatol. 2006 Jul;126(7):1450-8
pubmed: 16543901
Sci Rep. 2015 Aug 17;5:13114
pubmed: 26279470
Stem Cells. 2011 Aug;29(8):1256-68
pubmed: 21674699
J Invest Dermatol. 2006 Feb;126(2):497-502
pubmed: 16374449
World J Stem Cells. 2015 Mar 26;7(2):495-501
pubmed: 25815134
Stem Cell Res Ther. 2019 Jul 29;10(1):229
pubmed: 31358069