The role of altered fatty acid in pathological scars and their dermal fibroblasts

Purpose: The proposed pathological mechanism for scar formation is controversial, and increased attention has been paid to the fatty acids (FAs) in the formation of pathological scars. Notably, FAs are known to be important in inflammation and mechanotransduction, which is closely related to scar fo...

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Main Authors: Jin-Xiu Yang, Shi-Yi Li, Min-Liang Chen, Le-Ren He
Format: Article
Language:English
Published: Elsevier 2022-07-01
Series:Chinese Journal of Traumatology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S100812752200027X
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author Jin-Xiu Yang
Shi-Yi Li
Min-Liang Chen
Le-Ren He
author_facet Jin-Xiu Yang
Shi-Yi Li
Min-Liang Chen
Le-Ren He
author_sort Jin-Xiu Yang
collection DOAJ
description Purpose: The proposed pathological mechanism for scar formation is controversial, and increased attention has been paid to the fatty acids (FAs) in the formation of pathological scars. Notably, FAs are known to be important in inflammation and mechanotransduction, which is closely related to scar formation. Therefore, it is necessary to clarify the roles of FA in scar formation. Methods: Hypertrophic scar and keloid formed for more than a year and without other treatment, as well as normal skin samples were obtained from patients who underwent plastic surgery. Finally, keloids (n = 10), hypertrophic scars (n = 10), and normal skin samples (n = 10) were collected under informed consent. Primary dermal fibroblasts were isolated and cultured. The amount and variety of FAs were detected by lipid chromatography-mass spectrometry. Immunohistochemistry, real-time PCR, and western blotting were used to verify the expression of sterol regulatory element-binding protein-1 (SREBP1) and fatty acid synthase (FASN) in the samples and their fibroblasts. Student's t-test, ANOVA, and orthogonal partial least square discriminant analysis were performed for statistical analysis (∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). Results: Compared with full-thickness normal skin, there were 27 differential FAs in keloids and 15 differential FAs in hypertrophic scars (∗p < 0.05 and variable influence on projection >1.0). The expression of SREBP1 and FASN was lower in pathological scars both at mRNA and protein levels (all ∗p < 0.05). However, the mRNA levels of SREBP1 (∗∗∗p = 0.0002) and FASN (∗∗∗p = 0.0021) in keloid-derived fibroblasts were higher than that in normal skin fibroblasts (NFBs), while the expression in hypertrophic scar-derived fibroblasts was lower than that in NFBs (both ∗p < 0.05). Whereas there was no significant difference in FASN protein expression between keloid-derived fibroblasts and NFBs (p > 0.05). Conclusion: FAs involved in pathological scars are abnormally changed in scar formation. Thus, fatty acid-derived inflammation and de novo synthesis pathway of FA may play a key role in the formation of pathological scars.
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spelling doaj.art-44e853e693464e9680d307cbe0b22a1f2022-12-22T01:01:00ZengElsevierChinese Journal of Traumatology1008-12752022-07-01254218223The role of altered fatty acid in pathological scars and their dermal fibroblastsJin-Xiu Yang0Shi-Yi Li1Min-Liang Chen2Le-Ren He3Department of Burn and Plastic Surgery, The Fourth Medical Centre, Chinese PLA (People's Liberation Army) General Hospital, Beijing, 100038, China; 7th Department of Plastic Surgery, Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 10005, ChinaDepartment of Burn and Plastic Surgery, The Fourth Medical Centre, Chinese PLA (People's Liberation Army) General Hospital, Beijing, 100038, ChinaDepartment of Burn and Plastic Surgery, The Fourth Medical Centre, Chinese PLA (People's Liberation Army) General Hospital, Beijing, 100038, China; Corresponding author. Department of Burn and Plastic Surgery, the Fourth Medical Centre, Chinese PLA (People's Liberation Army), No. 51 Fucheng Road, General Hospital, Haidian District, Beijing, 100038, China.7th Department of Plastic Surgery, Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 10005, China; Corresponding author.Purpose: The proposed pathological mechanism for scar formation is controversial, and increased attention has been paid to the fatty acids (FAs) in the formation of pathological scars. Notably, FAs are known to be important in inflammation and mechanotransduction, which is closely related to scar formation. Therefore, it is necessary to clarify the roles of FA in scar formation. Methods: Hypertrophic scar and keloid formed for more than a year and without other treatment, as well as normal skin samples were obtained from patients who underwent plastic surgery. Finally, keloids (n = 10), hypertrophic scars (n = 10), and normal skin samples (n = 10) were collected under informed consent. Primary dermal fibroblasts were isolated and cultured. The amount and variety of FAs were detected by lipid chromatography-mass spectrometry. Immunohistochemistry, real-time PCR, and western blotting were used to verify the expression of sterol regulatory element-binding protein-1 (SREBP1) and fatty acid synthase (FASN) in the samples and their fibroblasts. Student's t-test, ANOVA, and orthogonal partial least square discriminant analysis were performed for statistical analysis (∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). Results: Compared with full-thickness normal skin, there were 27 differential FAs in keloids and 15 differential FAs in hypertrophic scars (∗p < 0.05 and variable influence on projection >1.0). The expression of SREBP1 and FASN was lower in pathological scars both at mRNA and protein levels (all ∗p < 0.05). However, the mRNA levels of SREBP1 (∗∗∗p = 0.0002) and FASN (∗∗∗p = 0.0021) in keloid-derived fibroblasts were higher than that in normal skin fibroblasts (NFBs), while the expression in hypertrophic scar-derived fibroblasts was lower than that in NFBs (both ∗p < 0.05). Whereas there was no significant difference in FASN protein expression between keloid-derived fibroblasts and NFBs (p > 0.05). Conclusion: FAs involved in pathological scars are abnormally changed in scar formation. Thus, fatty acid-derived inflammation and de novo synthesis pathway of FA may play a key role in the formation of pathological scars.http://www.sciencedirect.com/science/article/pii/S100812752200027XHypertrophic scarsKeloidsFatty acidsFibroblasts
spellingShingle Jin-Xiu Yang
Shi-Yi Li
Min-Liang Chen
Le-Ren He
The role of altered fatty acid in pathological scars and their dermal fibroblasts
Chinese Journal of Traumatology
Hypertrophic scars
Keloids
Fatty acids
Fibroblasts
title The role of altered fatty acid in pathological scars and their dermal fibroblasts
title_full The role of altered fatty acid in pathological scars and their dermal fibroblasts
title_fullStr The role of altered fatty acid in pathological scars and their dermal fibroblasts
title_full_unstemmed The role of altered fatty acid in pathological scars and their dermal fibroblasts
title_short The role of altered fatty acid in pathological scars and their dermal fibroblasts
title_sort role of altered fatty acid in pathological scars and their dermal fibroblasts
topic Hypertrophic scars
Keloids
Fatty acids
Fibroblasts
url http://www.sciencedirect.com/science/article/pii/S100812752200027X
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