补体c1酯酶抑制剂对马凡氏综合征小鼠无明显作用。

Vascular biology (Bristol, England) Pub Date : 2022-11-30 Print Date: 2022-11-01 DOI:10.1530/VB-22-0016
Stijntje Hibender, Siyu Li, Alex V Postma, Myrthe E Hoogeland, Denise Klaver, Richard B Pouw, Hans W Niessen, Antoine Hg Driessen, David R Koolbergen, Carlie Jm de Vries, Marieke Jh Baars, Arjan C Houweling, Paul A Krijnen, Vivian de Waard
{"title":"补体c1酯酶抑制剂对马凡氏综合征小鼠无明显作用。","authors":"Stijntje Hibender,&nbsp;Siyu Li,&nbsp;Alex V Postma,&nbsp;Myrthe E Hoogeland,&nbsp;Denise Klaver,&nbsp;Richard B Pouw,&nbsp;Hans W Niessen,&nbsp;Antoine Hg Driessen,&nbsp;David R Koolbergen,&nbsp;Carlie Jm de Vries,&nbsp;Marieke Jh Baars,&nbsp;Arjan C Houweling,&nbsp;Paul A Krijnen,&nbsp;Vivian de Waard","doi":"10.1530/VB-22-0016","DOIUrl":null,"url":null,"abstract":"<p><p>Marfan syndrome (MFS) is a connective tissue disorder causing aortic aneurysm formation. Currently, only prophylactic aortic surgery and blood pressure-lowering drugs are available to reduce the risk of aortic rupture. Upon whole genome sequencing of a Marfan family, we identified a complement gene C1R variant (p.Ser152Leu), which is associated with severe aortic patients. Therefore, we assessed the role of complement activation in MFS aortic tissue. Expression of various complement genes and proteins was detected in human and murine MFS aneurysm tissue, which prompted us to study complement inhibition in MFS mice. Treatment of the Fbn1C1041G/+ MFS mice with human plasma-derived C1-esterase inhibitor Cetor® resulted in reduced complement deposition, decreased macrophage influx in the aorta, and lower circulating TNFα levels. However, in line with previous anti-inflammatory treatments, complement inhibition did not change the aortic dilatation rate in this MFS mouse model. Thus, while complement factors/component 3 activation were detected in human/murine MFS aorta, Cetor® had no effect on aortic dilatation in MFS mice, indicating that complement inhibition is not a suitable treatment strategy in MFS.</p>","PeriodicalId":75294,"journal":{"name":"Vascular biology (Bristol, England)","volume":" ","pages":"40-49"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782404/pdf/","citationCount":"0","resultStr":"{\"title\":\"No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice.\",\"authors\":\"Stijntje Hibender,&nbsp;Siyu Li,&nbsp;Alex V Postma,&nbsp;Myrthe E Hoogeland,&nbsp;Denise Klaver,&nbsp;Richard B Pouw,&nbsp;Hans W Niessen,&nbsp;Antoine Hg Driessen,&nbsp;David R Koolbergen,&nbsp;Carlie Jm de Vries,&nbsp;Marieke Jh Baars,&nbsp;Arjan C Houweling,&nbsp;Paul A Krijnen,&nbsp;Vivian de Waard\",\"doi\":\"10.1530/VB-22-0016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Marfan syndrome (MFS) is a connective tissue disorder causing aortic aneurysm formation. Currently, only prophylactic aortic surgery and blood pressure-lowering drugs are available to reduce the risk of aortic rupture. Upon whole genome sequencing of a Marfan family, we identified a complement gene C1R variant (p.Ser152Leu), which is associated with severe aortic patients. Therefore, we assessed the role of complement activation in MFS aortic tissue. Expression of various complement genes and proteins was detected in human and murine MFS aneurysm tissue, which prompted us to study complement inhibition in MFS mice. Treatment of the Fbn1C1041G/+ MFS mice with human plasma-derived C1-esterase inhibitor Cetor® resulted in reduced complement deposition, decreased macrophage influx in the aorta, and lower circulating TNFα levels. However, in line with previous anti-inflammatory treatments, complement inhibition did not change the aortic dilatation rate in this MFS mouse model. Thus, while complement factors/component 3 activation were detected in human/murine MFS aorta, Cetor® had no effect on aortic dilatation in MFS mice, indicating that complement inhibition is not a suitable treatment strategy in MFS.</p>\",\"PeriodicalId\":75294,\"journal\":{\"name\":\"Vascular biology (Bristol, England)\",\"volume\":\" \",\"pages\":\"40-49\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782404/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vascular biology (Bristol, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1530/VB-22-0016\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/11/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vascular biology (Bristol, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1530/VB-22-0016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/11/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

马凡氏综合征(MFS)是一种导致主动脉瘤形成的结缔组织疾病。目前,只有预防性主动脉手术和降压药物可以降低主动脉破裂的风险。在对Marfan家族进行全基因组测序后,我们发现了一种补体基因C1R变体(p.Ser152Leu),它与严重主动脉瘤患者有关。因此,我们评估了补体激活在MFS主动脉组织中的作用。在人和小鼠MFS动脉瘤组织中检测到各种补体基因和蛋白质的表达,这促使我们研究MFS小鼠的补体抑制作用。用人血浆来源的C1酯酶抑制剂Cetor®治疗Fbn1C1041G/+MFS小鼠导致补体沉积减少,主动脉中巨噬细胞流入减少,循环TNFα水平降低。然而,与以前的抗炎治疗一致,补体抑制并没有改变该MFS小鼠模型的主动脉扩张率。因此,虽然在人/小鼠MFS主动脉中检测到补体因子/组分3激活,但Cetor®对MFS小鼠的主动脉扩张没有影响,这表明补体抑制不是MFS的合适治疗策略。
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
No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice.

Marfan syndrome (MFS) is a connective tissue disorder causing aortic aneurysm formation. Currently, only prophylactic aortic surgery and blood pressure-lowering drugs are available to reduce the risk of aortic rupture. Upon whole genome sequencing of a Marfan family, we identified a complement gene C1R variant (p.Ser152Leu), which is associated with severe aortic patients. Therefore, we assessed the role of complement activation in MFS aortic tissue. Expression of various complement genes and proteins was detected in human and murine MFS aneurysm tissue, which prompted us to study complement inhibition in MFS mice. Treatment of the Fbn1C1041G/+ MFS mice with human plasma-derived C1-esterase inhibitor Cetor® resulted in reduced complement deposition, decreased macrophage influx in the aorta, and lower circulating TNFα levels. However, in line with previous anti-inflammatory treatments, complement inhibition did not change the aortic dilatation rate in this MFS mouse model. Thus, while complement factors/component 3 activation were detected in human/murine MFS aorta, Cetor® had no effect on aortic dilatation in MFS mice, indicating that complement inhibition is not a suitable treatment strategy in MFS.

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
自引率
0.00%
发文量
0
审稿时长
13 weeks
期刊最新文献
Pharmacological and immunohistochemical characterization of dopamine D4 receptor in human umbilical artery and vein. Serum tissue plasminogen activator after cycling with blood flow restriction. Protection of liver sinusoidal endothelial cells using different preservation solutions. Lack of intracranial atherosclerosis in various atherosclerotic mouse models. Therapeutic angiogenesis for patients with chronic limb-threatening ischemia: promising or hoax?
×
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