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Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells

Pholiota nameko, a type of edible and medicinal fungus, is currently grown extensively for food and traditional medicine in China and Japan. It possesses various biological activities, such as anti-inflammatory, anti-hyperlipidemia and antitumor activities. However, P. nameko has rarely been discuss...

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Autores principales: Sung, Tzu-Jung, Wang, Yu-Ying, Liu, Kai-Lun, Chou, Chun-Hsu, Lai, Ping-Shan, Hsieh, Chang-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022505/
https://www.ncbi.nlm.nih.gov/pubmed/31936888
http://dx.doi.org/10.3390/antiox9010065
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author Sung, Tzu-Jung
Wang, Yu-Ying
Liu, Kai-Lun
Chou, Chun-Hsu
Lai, Ping-Shan
Hsieh, Chang-Wei
author_facet Sung, Tzu-Jung
Wang, Yu-Ying
Liu, Kai-Lun
Chou, Chun-Hsu
Lai, Ping-Shan
Hsieh, Chang-Wei
author_sort Sung, Tzu-Jung
collection PubMed
description Pholiota nameko, a type of edible and medicinal fungus, is currently grown extensively for food and traditional medicine in China and Japan. It possesses various biological activities, such as anti-inflammatory, anti-hyperlipidemia and antitumor activities. However, P. nameko has rarely been discussed in the field of dermatology; identifying its biological activities could be beneficial in development of a new natural ingredient used in wound care. To evaluate its in vitro wound healing activities, the present study assessed the antioxidant and anti-collagenase activities of P. nameko polysaccharides (PNPs) prepared through fractional precipitation (40%, 60% and 80% (v/v)); the assessments were conducted using reducing power, hydroxyl radical scavenging activity, dichloro-dihydro-fluorescein diacetate and collagenase activity assays. The ability of PNPs to facilitate L929 fibroblast cell proliferation and migration was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and scratch assays. The findings indicated that, among all fractions, PNP-80 showed the best antioxidant and anti-collagenase activity, as measured by their reducing power (IC(50) of PNP-80 was 2.43 ± 0.17 mg/mL), the hydroxyl radical scavenging (IC(50) of PNP-80 was 2.74 ± 0.11 mg/mL) and collagenase activity assay, and significantly reduced cellular ROS content, compared with that of H(2)O(2)-induced L929 cells. Moreover, PNP-80 significantly promoted L929 fibroblast proliferation and migration, compared with the control group. Overall, we suggested that PNP-80 could be a promising candidate for further evaluation of its potential application on wound healing.
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spelling pubmed-70225052020-03-09 Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells Sung, Tzu-Jung Wang, Yu-Ying Liu, Kai-Lun Chou, Chun-Hsu Lai, Ping-Shan Hsieh, Chang-Wei Antioxidants (Basel) Article Pholiota nameko, a type of edible and medicinal fungus, is currently grown extensively for food and traditional medicine in China and Japan. It possesses various biological activities, such as anti-inflammatory, anti-hyperlipidemia and antitumor activities. However, P. nameko has rarely been discussed in the field of dermatology; identifying its biological activities could be beneficial in development of a new natural ingredient used in wound care. To evaluate its in vitro wound healing activities, the present study assessed the antioxidant and anti-collagenase activities of P. nameko polysaccharides (PNPs) prepared through fractional precipitation (40%, 60% and 80% (v/v)); the assessments were conducted using reducing power, hydroxyl radical scavenging activity, dichloro-dihydro-fluorescein diacetate and collagenase activity assays. The ability of PNPs to facilitate L929 fibroblast cell proliferation and migration was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and scratch assays. The findings indicated that, among all fractions, PNP-80 showed the best antioxidant and anti-collagenase activity, as measured by their reducing power (IC(50) of PNP-80 was 2.43 ± 0.17 mg/mL), the hydroxyl radical scavenging (IC(50) of PNP-80 was 2.74 ± 0.11 mg/mL) and collagenase activity assay, and significantly reduced cellular ROS content, compared with that of H(2)O(2)-induced L929 cells. Moreover, PNP-80 significantly promoted L929 fibroblast proliferation and migration, compared with the control group. Overall, we suggested that PNP-80 could be a promising candidate for further evaluation of its potential application on wound healing. MDPI 2020-01-10 /pmc/articles/PMC7022505/ /pubmed/31936888 http://dx.doi.org/10.3390/antiox9010065 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sung, Tzu-Jung
Wang, Yu-Ying
Liu, Kai-Lun
Chou, Chun-Hsu
Lai, Ping-Shan
Hsieh, Chang-Wei
Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title_full Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title_fullStr Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title_full_unstemmed Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title_short Pholiota nameko Polysaccharides Promotes Cell Proliferation and Migration and Reduces ROS Content in H(2)O(2)-Induced L929 Cells
title_sort pholiota nameko polysaccharides promotes cell proliferation and migration and reduces ros content in h(2)o(2)-induced l929 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022505/
https://www.ncbi.nlm.nih.gov/pubmed/31936888
http://dx.doi.org/10.3390/antiox9010065
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