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层粘连蛋白 C 在腹主动脉瘤形成和进展中的表达和作用。

The expression and role of tenascin C in abdominal aortic aneurysm formation and progression.

机构信息

Ludwig Boltzmann Institute for Cardiovascular Research, Center for Biomedical Research, Medical University of Vienna, Vienna, Austria.

Department of Cardiac Surgery, University Hospital St. Pölten, Karl Landsteiner University, St. Pölten, Austria.

出版信息

Interact Cardiovasc Thorac Surg. 2022 May 2;34(5):841-848. doi: 10.1093/icvts/ivac018.

Abstract

OBJECTIVES

Up-regulation of tenascin C (TNC), a matricellular protein, produced mainly by vascular smooth muscle cells (VSMC), is associated with the progression and dilation of abdominal aortic aneurysms (AAA). The aims of this study were (i) to evaluate whether serum levels of TNC in patients with AAA patients correlate with aortic diameter and (ii) to clarify the role of TNC in formation and progression of AAA in a murine model.

METHODS

In 15 patients with AAA serum levels of TNC were measured and correlated with aortic diameters. Moreover, in a murine calcium chloride AAA model, the impact of TNC deficiency on AAA diameter was evaluated. Finally, human VSMC were incubated with TNC to clarify its regulating potential.

RESULTS

In the clinical cohort, there was a trend of correlation between serum TNC levels and AAA diameter (P = 0.055). TNC knock out mice with AAA showed significantly lower diameter ratios compared to the wild-type group (WT) 3 weeks (P < 0.05) and 10 weeks (P < 0.05) after AAA induction. Immunohistochemistry revealed increased TNC expression in aortic tissue from WT with AAA as compared sham-operated mice. Furthermore, WT with AAA showed a more disrupted Elastin structure than TNC knock out mice 10 weeks after AAA induction. In human aortic VSMC, TNC incubation induced expression of remodelling associated proteins.

CONCLUSIONS

TNC might play a causative role in the formation, dilation and progression of AAA. Our results indicate that TNC might be a biomarker as well as a potential therapeutic target in the treatment of AAA.

摘要

目的

细胞外基质蛋白 tenascin C(TNC)主要由血管平滑肌细胞(VSMC)产生,其表达上调与腹主动脉瘤(AAA)的进展和扩张有关。本研究的目的是:(i)评估 AAA 患者的血清 TNC 水平与主动脉直径是否相关;(ii)阐明 TNC 在 AAA 形成和进展中的作用。

方法

在 15 名 AAA 患者中测量了血清 TNC 水平,并与主动脉直径相关联。此外,在小鼠氯化钙 AAA 模型中,评估了 TNC 缺乏对 AAA 直径的影响。最后,培养人 VSMC 以阐明其调节潜能。

结果

在临床队列中,血清 TNC 水平与 AAA 直径呈趋势相关(P = 0.055)。与野生型(WT)组相比,AAA 后 3 周(P < 0.05)和 10 周(P < 0.05),TNC 敲除小鼠的 AAA 直径比明显较低。免疫组织化学显示 WT 组 AAA 患者的主动脉组织中 TNC 表达增加,而与假手术组相比。此外,与 TNC 敲除小鼠相比,WT 组在 AAA 诱导 10 周后,弹性蛋白结构破坏更严重。在人主动脉 VSMC 中,TNC 孵育诱导了重塑相关蛋白的表达。

结论

TNC 可能在 AAA 的形成、扩张和进展中起因果作用。我们的结果表明,TNC 可能是治疗 AAA 的生物标志物和潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6b/9070497/e9ecc23c47a4/ivac018f7.jpg

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