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在微血管重塑过程中,小静脉周围的血管周细胞上调NG2表达。

Perivascular cells along venules upregulate NG2 expression during microvascular remodeling.

作者信息

Murfee Walter L, Rehorn Michael R, Peirce Shayn M, Skalak Thomas C

机构信息

Department of Biomedical Engineering, University of Virginia, Health System, Charlottesville, Virginia 22908, USA.

出版信息

Microcirculation. 2006 Apr-May;13(3):261-73. doi: 10.1080/10739680600559153.

Abstract

OBJECTIVE

Recently the authors have shown that neuron-glial antigen 2 (NG2) is expressed by perivascular cells along arterioles and capillaries, but not along venules in quiescent rat mesenteric microvascular networks. To investigate how the spatial distribution of this proteoglycan changes during microvascular remodeling, the objective of this study was to characterize the expression of NG2 in adult rat mesenteric microvascular networks undergoing active remodeling.

METHODS

The distribution of NG2 expression was evaluated in adult rat mesenteric microvascular networks. Tissues were harvested from 250 g, female, Sprague-Dawley rats at 1, 3, and 5 days poststimulation and double immunolabeled for NG2 and CD31 (endothelial cell marker).

RESULTS

After 1 day, NG2 expression was observed along 27 +/- 11% of network draining venules (14-55 microm) and after 3 days, 59 +/- 10% of draining venules (13-59 microm) stained positive for the proteoglycan. By 5 days poststimulation, the percentage of network draining venules (18-59 microm) staining positive for NG2 returned to 18 +/- 7%, indicating a downregulation of the proteoglycan toward quiescent levels along larger-sized venules.

CONCLUSIONS

The results suggest that NG2 proteoglycan expression is transiently upregulated along venules during microvascular remodeling, implicating NG2 as a marker of activated venules.

摘要

目的

最近作者发现,在静止的大鼠肠系膜微血管网络中,神经胶质抗原2(NG2)由小动脉和毛细血管周围的细胞表达,但小静脉周围的细胞不表达。为了研究这种蛋白聚糖的空间分布在微血管重塑过程中如何变化,本研究的目的是表征NG2在经历活跃重塑的成年大鼠肠系膜微血管网络中的表达。

方法

评估成年大鼠肠系膜微血管网络中NG2表达的分布。在刺激后1、3和5天从250 g雌性Sprague-Dawley大鼠中采集组织,并对NG2和CD31(内皮细胞标记物)进行双重免疫标记。

结果

1天后,在27±11%的引流小静脉(14 - 55微米)中观察到NG2表达,3天后,59±10%的引流小静脉(13 - 59微米)对该蛋白聚糖染色呈阳性。到刺激后5天,对NG2染色呈阳性的引流小静脉(18 - 59微米)的百分比恢复到18±7%,表明沿着较大尺寸的小静脉,该蛋白聚糖朝着静止水平下调。

结论

结果表明,在微血管重塑过程中,NG2蛋白聚糖在小静脉中的表达短暂上调,这意味着NG2是活化小静脉的标志物。

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