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多功能蛋白聚糖定位于增殖间充质细胞的细胞核中。

Versican localizes to the nucleus in proliferating mesenchymal cells.

作者信息

Carthy Jon M, Abraham Thomas, Meredith Anna J, Boroomand Seti, McManus Bruce M

机构信息

UBC James Hogg Research Centre, Institute for Heart+Lung Health, Department of Pathology and Laboratory Medicine, University of British Columbia, Providence Health Care, Vancouver, BC, Canada.

UBC James Hogg Research Centre, Institute for Heart+Lung Health, Department of Pathology and Laboratory Medicine, University of British Columbia, Providence Health Care, Vancouver, BC, Canada.

出版信息

Cardiovasc Pathol. 2015 Nov-Dec;24(6):368-74. doi: 10.1016/j.carpath.2015.07.010. Epub 2015 Aug 7.

Abstract

OBJECTIVE

Versican is a versatile and highly interactive chondroitin sulfate proteoglycan that is found in the extracellular matrix (ECM) of many tissues and is a major component of developing and developed lesions in atherosclerotic vascular disease. In this paper, we present data to indicate that versican may have important intracellular functions in addition to its better known roles in the ECM.

METHODS AND RESULTS

Rat aortic smooth muscle cells were fixed and immunostained for versican and images of fluorescently labeled cells were obtained by confocal microscopy. Intracellular versican was detected in the nucleus and cytosol of vascular smooth muscle cells. The use of a synthetic neutralizing peptide eliminated versican immunostaining, demonstrating the specificity of the antibody used in this study. Western blot of pure nuclear extracts confirmed the presence of versican in the nucleus, and multifluorescent immunostaining showed strong colocalization of versican and nucleolin, suggesting a nucleolar localization of versican in nondividing cells. In dividing valve interstitial cells, a strong signal for versican was observed in and around the condensed chromosomes during the various stages of mitosis. Multifluorescent immunostaining for versican and tubulin revealed versican aggregated at opposing poles of the mitotic spindle during metaphase. Knockdown of versican expression using siRNA disrupted the organization of the mitotic spindle and led to the formation of multipolar spindles during metaphase.

CONCLUSIONS

Collectively, these data suggest an intracellular function for versican in vascular cells where it appears to play a role in mitotic spindle organization during cell division. These observations open a new avenue for studies of versican, suggesting even more diverse roles in vascular health and disease.

摘要

目的

多功能蛋白聚糖是一种多功能且具有高度相互作用的硫酸软骨素蛋白聚糖,存在于许多组织的细胞外基质(ECM)中,是动脉粥样硬化性血管疾病中正在形成和已形成病变的主要成分。在本文中,我们提供的数据表明,多功能蛋白聚糖除了在细胞外基质中发挥其广为人知的作用外,可能还具有重要的细胞内功能。

方法与结果

将大鼠主动脉平滑肌细胞固定,并用多功能蛋白聚糖进行免疫染色,通过共聚焦显微镜获得荧光标记细胞的图像。在血管平滑肌细胞的细胞核和细胞质中检测到细胞内多功能蛋白聚糖。使用合成中和肽消除了多功能蛋白聚糖免疫染色,证明了本研究中使用抗体的特异性。对纯核提取物进行的蛋白质印迹证实细胞核中存在多功能蛋白聚糖,多重荧光免疫染色显示多功能蛋白聚糖与核仁素强烈共定位,表明在非分裂细胞中多功能蛋白聚糖定位于核仁。在分裂的瓣膜间质细胞中,在有丝分裂的各个阶段,在浓缩染色体及其周围观察到多功能蛋白聚糖的强信号。对多功能蛋白聚糖和微管蛋白进行多重荧光免疫染色显示,在中期多功能蛋白聚糖聚集在有丝分裂纺锤体的相对两极。使用小干扰RNA(siRNA)敲低多功能蛋白聚糖表达会破坏有丝分裂纺锤体的组织,并导致中期形成多极纺锤体。

结论

总体而言,这些数据表明多功能蛋白聚糖在血管细胞中具有细胞内功能,在细胞分裂过程中似乎在有丝分裂纺锤体组织中发挥作用。这些观察结果为多功能蛋白聚糖的研究开辟了一条新途径,表明其在血管健康和疾病中发挥着更多样化的作用。

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