Cargando…
Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells?
BACKGROUND: The interaction between activated microglia and T lymphocytes can yield abundant pro-inflammatory cytokines. Our previous study proved that thymus immune tolerance could alleviate the inflammatory response. This study aimed to investigate whether intrathymic injection of myelin basic pro...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819305/ https://www.ncbi.nlm.nih.gov/pubmed/26996480 http://dx.doi.org/10.4103/0366-6999.178955 |
_version_ | 1782425176613322752 |
---|---|
author | Cui, Zhan-Qun Liu, Bao-Long Wu, Qiao-Li Cai, Ying Fan, Wei-Jia Zhang, Ming-Chao Ding, Wei-Liang Zhang, Bo Kang, Jian-Min Yan, Hua |
author_facet | Cui, Zhan-Qun Liu, Bao-Long Wu, Qiao-Li Cai, Ying Fan, Wei-Jia Zhang, Ming-Chao Ding, Wei-Liang Zhang, Bo Kang, Jian-Min Yan, Hua |
author_sort | Cui, Zhan-Qun |
collection | PubMed |
description | BACKGROUND: The interaction between activated microglia and T lymphocytes can yield abundant pro-inflammatory cytokines. Our previous study proved that thymus immune tolerance could alleviate the inflammatory response. This study aimed to investigate whether intrathymic injection of myelin basic protein (MBP) in mice could suppress the inflammatory response after co-culture of T lymphocytes and BV-2 microglia cells. METHODS: Totally, 72 male C57BL/6 mice were randomly assigned to three groups (n = 24 in each): Group A: intrathymic injection of 100 μl MBP (1 mg/ml); Group B: intrathymic injection of 100 μl phosphate-buffered saline (PBS); and Group C: sham operation group. Every eight mice in each group were sacrificed to obtain the spleen at postoperative days 3, 7, and 14, respectively. T lymphocytes those were extracted and purified from the spleens were then co-cultured with activated BV-2 microglia cells at a proportion of 1:2 in the medium containing MBP for 3 days. After identified the T lymphocytes by CD3, surface antigens of T lymphocytes (CD4, CD8, CD152, and CD154) and BV-2 microglia cells (CD45 and CD54) were detected by flow cytometry. The expressions of pro-inflammatory factors of BV-2 microglia cells (interleukin [IL]-1β, tumor necrosis factor-α [TNF-α], and inducible nitric oxide synthase [iNOS]) were detected by quantitative real-time polymerase chain reaction (PCR). One-way analysis of variance (ANOVA) and the least significant difference test were used for data analysis. RESULTS: The levels of CD152 in Group A showed an upward trend from the 3(rd) to 7(th) day, with a downward trend from the 7(th) to 14(th) day (20.12 ± 0.71%, 30.71 ± 1.14%, 13.50 ± 0.71% at postoperative days 3, 7, and 14, respectively, P < 0.05). The levels of CD154 in Group A showed a downward trend from the 3(rd) to 7(th) day, with an upward trend from the 7(th) to 14(th) day (10.00 ± 0.23%, 5.28 ± 0.69%, 14.67 ± 2.71% at postoperative days 3, 7, and 14, respectively, P < 0.05). The ratio of CD4(+)/CD8 + T in Group A showed a downward trend from the 3(rd) to 7(th) day, with the minimum at postoperative day 7, then an upward trend from the 7(th) to 14(th) day (P < 0.05). Meanwhile, the levels of CD45 and CD54 in Group A were found as the same trend as the ratio of CD4(+)/CD8 + T (CD45: 83.39 ± 2.56%, 82.74 ± 2.09%, 87.56 ± 2.11%; CD54: 3.80 ± 0.24%, 0.94 ± 0.40%, 3.41 ± 0.33% at postoperative days 3, 7, and 14, respectively, P < 0.05). The expressions of TNF-α, IL-1β, and iNOS in Group A were significantly lower than those in Groups B and C, and the values at postoperative day 7 were the lowest compared with those at postoperative days 3 and 14 (P < 0.05). No significant difference was found between Groups B and C. CONCLUSIONS: Intrathymic injection of MBP could suppress the immune reaction that might reduce the secondary immune injury of brain tissue induced by an inflammatory response. |
format | Online Article Text |
id | pubmed-4819305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48193052016-04-05 Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? Cui, Zhan-Qun Liu, Bao-Long Wu, Qiao-Li Cai, Ying Fan, Wei-Jia Zhang, Ming-Chao Ding, Wei-Liang Zhang, Bo Kang, Jian-Min Yan, Hua Chin Med J (Engl) Original Article BACKGROUND: The interaction between activated microglia and T lymphocytes can yield abundant pro-inflammatory cytokines. Our previous study proved that thymus immune tolerance could alleviate the inflammatory response. This study aimed to investigate whether intrathymic injection of myelin basic protein (MBP) in mice could suppress the inflammatory response after co-culture of T lymphocytes and BV-2 microglia cells. METHODS: Totally, 72 male C57BL/6 mice were randomly assigned to three groups (n = 24 in each): Group A: intrathymic injection of 100 μl MBP (1 mg/ml); Group B: intrathymic injection of 100 μl phosphate-buffered saline (PBS); and Group C: sham operation group. Every eight mice in each group were sacrificed to obtain the spleen at postoperative days 3, 7, and 14, respectively. T lymphocytes those were extracted and purified from the spleens were then co-cultured with activated BV-2 microglia cells at a proportion of 1:2 in the medium containing MBP for 3 days. After identified the T lymphocytes by CD3, surface antigens of T lymphocytes (CD4, CD8, CD152, and CD154) and BV-2 microglia cells (CD45 and CD54) were detected by flow cytometry. The expressions of pro-inflammatory factors of BV-2 microglia cells (interleukin [IL]-1β, tumor necrosis factor-α [TNF-α], and inducible nitric oxide synthase [iNOS]) were detected by quantitative real-time polymerase chain reaction (PCR). One-way analysis of variance (ANOVA) and the least significant difference test were used for data analysis. RESULTS: The levels of CD152 in Group A showed an upward trend from the 3(rd) to 7(th) day, with a downward trend from the 7(th) to 14(th) day (20.12 ± 0.71%, 30.71 ± 1.14%, 13.50 ± 0.71% at postoperative days 3, 7, and 14, respectively, P < 0.05). The levels of CD154 in Group A showed a downward trend from the 3(rd) to 7(th) day, with an upward trend from the 7(th) to 14(th) day (10.00 ± 0.23%, 5.28 ± 0.69%, 14.67 ± 2.71% at postoperative days 3, 7, and 14, respectively, P < 0.05). The ratio of CD4(+)/CD8 + T in Group A showed a downward trend from the 3(rd) to 7(th) day, with the minimum at postoperative day 7, then an upward trend from the 7(th) to 14(th) day (P < 0.05). Meanwhile, the levels of CD45 and CD54 in Group A were found as the same trend as the ratio of CD4(+)/CD8 + T (CD45: 83.39 ± 2.56%, 82.74 ± 2.09%, 87.56 ± 2.11%; CD54: 3.80 ± 0.24%, 0.94 ± 0.40%, 3.41 ± 0.33% at postoperative days 3, 7, and 14, respectively, P < 0.05). The expressions of TNF-α, IL-1β, and iNOS in Group A were significantly lower than those in Groups B and C, and the values at postoperative day 7 were the lowest compared with those at postoperative days 3 and 14 (P < 0.05). No significant difference was found between Groups B and C. CONCLUSIONS: Intrathymic injection of MBP could suppress the immune reaction that might reduce the secondary immune injury of brain tissue induced by an inflammatory response. Medknow Publications & Media Pvt Ltd 2016-04-05 /pmc/articles/PMC4819305/ /pubmed/26996480 http://dx.doi.org/10.4103/0366-6999.178955 Text en Copyright: © 2016 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Cui, Zhan-Qun Liu, Bao-Long Wu, Qiao-Li Cai, Ying Fan, Wei-Jia Zhang, Ming-Chao Ding, Wei-Liang Zhang, Bo Kang, Jian-Min Yan, Hua Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title | Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title_full | Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title_fullStr | Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title_full_unstemmed | Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title_short | Could Intrathymic Injection of Myelin Basic Protein Suppress Inflammatory Response After Co-culture of T Lymphocytes and BV-2 Microglia Cells? |
title_sort | could intrathymic injection of myelin basic protein suppress inflammatory response after co-culture of t lymphocytes and bv-2 microglia cells? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819305/ https://www.ncbi.nlm.nih.gov/pubmed/26996480 http://dx.doi.org/10.4103/0366-6999.178955 |
work_keys_str_mv | AT cuizhanqun couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT liubaolong couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT wuqiaoli couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT caiying couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT fanweijia couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT zhangmingchao couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT dingweiliang couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT zhangbo couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT kangjianmin couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells AT yanhua couldintrathymicinjectionofmyelinbasicproteinsuppressinflammatoryresponseaftercocultureoftlymphocytesandbv2microgliacells |