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Macrophage phenotypes and Gas6/Axl signaling in apical lesions
BACKGROUND/PURPOSE: Macrophages participate in the periapical inflammation with pro-inflammatory M1 cells and anti-inflammatory M2 cells. Gas6/Axl signal is the responsible pathway for the activation of M1 and polarization of M2. The aim of this study was to compare the number of CD16(+) M1 cells, C...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Association for Dental Sciences of the Republic of China
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739459/ https://www.ncbi.nlm.nih.gov/pubmed/31528256 http://dx.doi.org/10.1016/j.jds.2018.12.002 |
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author | Chen, Szu-Yu Chiang, Chi-Fu Chiu, Kou-Chou Cheng, Chao-Wen Huang, Shih-Ming Chen, Pei-Hsuan Chen, Ching-Yang Shieh, Yi-Shing |
author_facet | Chen, Szu-Yu Chiang, Chi-Fu Chiu, Kou-Chou Cheng, Chao-Wen Huang, Shih-Ming Chen, Pei-Hsuan Chen, Ching-Yang Shieh, Yi-Shing |
author_sort | Chen, Szu-Yu |
collection | PubMed |
description | BACKGROUND/PURPOSE: Macrophages participate in the periapical inflammation with pro-inflammatory M1 cells and anti-inflammatory M2 cells. Gas6/Axl signal is the responsible pathway for the activation of M1 and polarization of M2. The aim of this study was to compare the number of CD16(+) M1 cells, CD206(+) M2 cells, and Gas6/Axl expression between apical granulomas and radicular cysts. MATERIALS AND METHODS: Twenty-four cases of granuloma and twenty of cysts were submitted to immunohistochemistry using anti-CD16 and anti-CD206 antibodies for determining M1 and M2 macrophages and investigating the cells with positive Gas6 and Axl expression. RESULTS: There were more numerous of M1 macrophages in radicular cysts (175.9 ± 87.7) compared to apical granuloma (116.6 ± 55.8), and M2 macrophages was higher in cysts (204.0 ± 97.6) than granuloma (152.9 ± 64.6). The level of Gas6/Axl expression were similar. There was a significant different in M1 macrophage (P = 0.014) between two diagnosis. In patients with or without root resorption, the number of M1 were 194.6 ± 57.2 compared with 139.1 ± 79.6. The number of M2 were 241.7 ± 81.4 and 164.6 ± 77.1. The expression of Axl was stronger in root resorption patients (191.1 ± 43.6), but the tendency in Gas6 expression was similar. Significant differences were noted in high M2 infiltration and Axl positive lesions. CONCLUSION: It appears that macrophages associated with significantly higher numbers in radicular cysts than apical granuloma. Meanwhile, macrophages and Axl receptor was intensively expressed in patients with root resorption, related to severe inflammation. |
format | Online Article Text |
id | pubmed-6739459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Association for Dental Sciences of the Republic of China |
record_format | MEDLINE/PubMed |
spelling | pubmed-67394592019-09-16 Macrophage phenotypes and Gas6/Axl signaling in apical lesions Chen, Szu-Yu Chiang, Chi-Fu Chiu, Kou-Chou Cheng, Chao-Wen Huang, Shih-Ming Chen, Pei-Hsuan Chen, Ching-Yang Shieh, Yi-Shing J Dent Sci Original Article BACKGROUND/PURPOSE: Macrophages participate in the periapical inflammation with pro-inflammatory M1 cells and anti-inflammatory M2 cells. Gas6/Axl signal is the responsible pathway for the activation of M1 and polarization of M2. The aim of this study was to compare the number of CD16(+) M1 cells, CD206(+) M2 cells, and Gas6/Axl expression between apical granulomas and radicular cysts. MATERIALS AND METHODS: Twenty-four cases of granuloma and twenty of cysts were submitted to immunohistochemistry using anti-CD16 and anti-CD206 antibodies for determining M1 and M2 macrophages and investigating the cells with positive Gas6 and Axl expression. RESULTS: There were more numerous of M1 macrophages in radicular cysts (175.9 ± 87.7) compared to apical granuloma (116.6 ± 55.8), and M2 macrophages was higher in cysts (204.0 ± 97.6) than granuloma (152.9 ± 64.6). The level of Gas6/Axl expression were similar. There was a significant different in M1 macrophage (P = 0.014) between two diagnosis. In patients with or without root resorption, the number of M1 were 194.6 ± 57.2 compared with 139.1 ± 79.6. The number of M2 were 241.7 ± 81.4 and 164.6 ± 77.1. The expression of Axl was stronger in root resorption patients (191.1 ± 43.6), but the tendency in Gas6 expression was similar. Significant differences were noted in high M2 infiltration and Axl positive lesions. CONCLUSION: It appears that macrophages associated with significantly higher numbers in radicular cysts than apical granuloma. Meanwhile, macrophages and Axl receptor was intensively expressed in patients with root resorption, related to severe inflammation. Association for Dental Sciences of the Republic of China 2019-09 2019-04-04 /pmc/articles/PMC6739459/ /pubmed/31528256 http://dx.doi.org/10.1016/j.jds.2018.12.002 Text en © 2019 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Chen, Szu-Yu Chiang, Chi-Fu Chiu, Kou-Chou Cheng, Chao-Wen Huang, Shih-Ming Chen, Pei-Hsuan Chen, Ching-Yang Shieh, Yi-Shing Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title | Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title_full | Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title_fullStr | Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title_full_unstemmed | Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title_short | Macrophage phenotypes and Gas6/Axl signaling in apical lesions |
title_sort | macrophage phenotypes and gas6/axl signaling in apical lesions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739459/ https://www.ncbi.nlm.nih.gov/pubmed/31528256 http://dx.doi.org/10.1016/j.jds.2018.12.002 |
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