在慢性哮喘大鼠模型中,全身给药 c-Kit+ 细胞可减轻肺部和血管炎症。

IF 2.4 3区 生物学 Q4 CELL BIOLOGY BMC Molecular and Cell Biology Pub Date : 2022-02-24 DOI:10.1186/s12860-022-00410-z
Sajjad Taghizadeh, Rana Keyhanmanesh, Reza Rahbarghazi, Jafar Rezaie, Aref Delkhosh, Mehdi Hassanpour, Hossein Heiran, Arshad Ghaffari-Nasab, Mahdi Ahmadi
{"title":"在慢性哮喘大鼠模型中,全身给药 c-Kit+ 细胞可减轻肺部和血管炎症。","authors":"Sajjad Taghizadeh, Rana Keyhanmanesh, Reza Rahbarghazi, Jafar Rezaie, Aref Delkhosh, Mehdi Hassanpour, Hossein Heiran, Arshad Ghaffari-Nasab, Mahdi Ahmadi","doi":"10.1186/s12860-022-00410-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>To circumvent some pitfalls related to acute status, chronic model of asthma is conceived to be more suitable approach to guarantee the conditions which are similar to human pulmonary disease. Here, possible therapeutic mechanisms were monitored by which c-kit<sup>+</sup> bone marrow cells can attenuate vascular inflammation in rat model of chronic asthma.</p><p><strong>Results: </strong>Data revealed c-Kit<sup>+</sup> cells could significantly reduce pathological injures in asthmatic rats via modulating the expression of IL-4, INF-γ, ICAM-1 and VCAM-1 in lung tissues and TNF-α, IL-1β and NO levels in BALF (p < 0.001 to p < 0.05). Besides, c-Kit<sup>+</sup> cells reduced increased levels of VCAM-1 evaluated by immunohistochemistry staining. In contrast to c-Kit<sup>+</sup> cells, c-Kit<sup>-</sup> cells could not exert beneficial effects in the asthmatic conditions.</p><p><strong>Conclusion: </strong>Overall, we found that systemic administration of C-kit positive cells can diminish pulmonary and vascular inflammation of chronic asthmatic changes in a rat model. These cells are eligible to suppress inflammation and nitrosative stress in lung tissue coincides with the reduction of pathological changes. These data indicate that C-kit positive cells be used as an alternative cell source for the amelioration of asthmatic changes.</p>","PeriodicalId":9099,"journal":{"name":"BMC Molecular and Cell Biology","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2022-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876378/pdf/","citationCount":"0","resultStr":"{\"title\":\"Systemic administration of c-Kit<sup>+</sup> cells diminished pulmonary and vascular inflammation in rat model of chronic asthma.\",\"authors\":\"Sajjad Taghizadeh, Rana Keyhanmanesh, Reza Rahbarghazi, Jafar Rezaie, Aref Delkhosh, Mehdi Hassanpour, Hossein Heiran, Arshad Ghaffari-Nasab, Mahdi Ahmadi\",\"doi\":\"10.1186/s12860-022-00410-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>To circumvent some pitfalls related to acute status, chronic model of asthma is conceived to be more suitable approach to guarantee the conditions which are similar to human pulmonary disease. Here, possible therapeutic mechanisms were monitored by which c-kit<sup>+</sup> bone marrow cells can attenuate vascular inflammation in rat model of chronic asthma.</p><p><strong>Results: </strong>Data revealed c-Kit<sup>+</sup> cells could significantly reduce pathological injures in asthmatic rats via modulating the expression of IL-4, INF-γ, ICAM-1 and VCAM-1 in lung tissues and TNF-α, IL-1β and NO levels in BALF (p < 0.001 to p < 0.05). Besides, c-Kit<sup>+</sup> cells reduced increased levels of VCAM-1 evaluated by immunohistochemistry staining. In contrast to c-Kit<sup>+</sup> cells, c-Kit<sup>-</sup> cells could not exert beneficial effects in the asthmatic conditions.</p><p><strong>Conclusion: </strong>Overall, we found that systemic administration of C-kit positive cells can diminish pulmonary and vascular inflammation of chronic asthmatic changes in a rat model. These cells are eligible to suppress inflammation and nitrosative stress in lung tissue coincides with the reduction of pathological changes. These data indicate that C-kit positive cells be used as an alternative cell source for the amelioration of asthmatic changes.</p>\",\"PeriodicalId\":9099,\"journal\":{\"name\":\"BMC Molecular and Cell Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2022-02-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876378/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Molecular and Cell Biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s12860-022-00410-z\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Molecular and Cell Biology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12860-022-00410-z","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:为了避免与急性状态相关的一些缺陷,慢性哮喘模型被认为是更适合的方法,以保证与人类肺部疾病相似的条件。本文研究了 c-kit+ 骨髓细胞在慢性哮喘大鼠模型中减轻血管炎症的可能治疗机制:结果:数据显示,c-Kit+细胞可通过调节肺组织中IL-4、INF-γ、ICAM-1和VCAM-1的表达以及BALF中TNF-α、IL-1β和NO的水平,显著减轻哮喘大鼠的病理损伤。与 c-Kit+ 细胞相反,c-Kit- 细胞不能对哮喘患者产生有益影响:总之,我们发现在大鼠模型中,全身给药 C-kit 阳性细胞可减轻慢性哮喘病变的肺部和血管炎症。这些细胞有资格抑制肺组织中的炎症和亚硝酸应激,与病理变化的减少相吻合。这些数据表明,C-kit 阳性细胞可用作改善哮喘病变的替代细胞来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Systemic administration of c-Kit+ cells diminished pulmonary and vascular inflammation in rat model of chronic asthma.

Background: To circumvent some pitfalls related to acute status, chronic model of asthma is conceived to be more suitable approach to guarantee the conditions which are similar to human pulmonary disease. Here, possible therapeutic mechanisms were monitored by which c-kit+ bone marrow cells can attenuate vascular inflammation in rat model of chronic asthma.

Results: Data revealed c-Kit+ cells could significantly reduce pathological injures in asthmatic rats via modulating the expression of IL-4, INF-γ, ICAM-1 and VCAM-1 in lung tissues and TNF-α, IL-1β and NO levels in BALF (p < 0.001 to p < 0.05). Besides, c-Kit+ cells reduced increased levels of VCAM-1 evaluated by immunohistochemistry staining. In contrast to c-Kit+ cells, c-Kit- cells could not exert beneficial effects in the asthmatic conditions.

Conclusion: Overall, we found that systemic administration of C-kit positive cells can diminish pulmonary and vascular inflammation of chronic asthmatic changes in a rat model. These cells are eligible to suppress inflammation and nitrosative stress in lung tissue coincides with the reduction of pathological changes. These data indicate that C-kit positive cells be used as an alternative cell source for the amelioration of asthmatic changes.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
BMC Molecular and Cell Biology
BMC Molecular and Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
5.50
自引率
0.00%
发文量
46
审稿时长
27 weeks
期刊最新文献
Optimisation of cryopreservation conditions, including storage duration and revival methods, for the viability of human primary cells. Differential methylation patterns in paternally imprinted gene promoter regions in sperm from hepatitis B virus infected individuals. Circulating microRNAs as potential biomarkers of physical activity in geriatric patients with HCV. Correction: The primary cilium dampens proliferative signaling and represses a G2/M transcriptional network in quiescent myoblasts. Upregulated dual oxidase 1-induced oxidative stress and caspase-1-dependent pyroptosis reflect the etiologies of heart failure
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1