Volume 11, Issue 12 e201800174
FULL ARTICLE

Photobiomodulation therapy promotes in vitro wound healing in nicastrin KO HaCaT cells

Paola M. Tricarico

Corresponding Author

Paola M. Tricarico

University of Trieste, Trieste, Italy

Correspondence

Paola M. Tricarico, University of Trieste, Piazzale Europa 1, 34138 Trieste, Italy.

Email: [email protected]

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Luisa Zupin

Luisa Zupin

University of Trieste, Trieste, Italy

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Giulia Ottaviani

Giulia Ottaviani

University of Trieste, Trieste, Italy

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Sabrina Pacor

Sabrina Pacor

University of Trieste, Trieste, Italy

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Francette Jean-Louis

Francette Jean-Louis

INSERM U955 Eq.16, Institut Mondor de Recherche Biomédicale and VRI (Vaccine Research Institute), Créteil, France

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Michele Boniotto

Michele Boniotto

INSERM U955 Eq. 16, Institut Mondor de Recherche Biomédicale and Université Paris Est-Créteil (UPEC), Faculté de Médecine, Créteil, France

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Sergio Crovella

Sergio Crovella

University of Trieste, Trieste, Italy

Institute for Maternal and Child Health "Burlo Garofolo", Trieste, Italy

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First published: 02 July 2018
Citations: 8
Michele Boniotto and Sergio Crovella contributed equally to this study.
Funding information University funding for scientific research project, Grant/Award Number: U22SCFRA15 and IRCCS Burlo Garofolo/Italian Ministry of Health (RC 15/2017)

Abstract

Mutations in NCSTN gene (encoding for nicastrin protein) are associated with hidradenitis suppurativa (HS), a chronic inflammatory disease involving hair follicles. HS is clinically handled with drugs but the most severe cases are treated with surgery. Photobiomodulation (PBM) therapy, already used in the treatment of skin diseases such as acne, herpes virus lesions, ultraviolet damage, vitiligo, hypertrophic scar, keloid, burn, psoriasis and diabetic chronic wounds, could be beneficial as an adjuvant supportive treatment to promote and foster the healing process after skin excision in HS. The effects of PBM therapy in promoting the wound closure are evaluated in a HaCaT cells NCSTN/−, assessing cell metabolism, migration rate, proliferation and cell cycle progression. In our experimental model, PBM exerts a potent action on metabolism of mutated keratinocytes, incrementing adenosine triphosphate (ATP) production at 2 hours, while after 24 hours an increase of metabolism with a decrement of intracellular ATP levels were recorded. Moreover, PBM speeds up the wound closure, inducing cells' migration without affecting their proliferation.Based on our findings, we suggest the use of PBM in HS patients, who undergo major surgery with large skin excision.

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