Molecular and Functional Characterization of Caveolae in Mixed Cultures of Human NT-2 Neurons and Astrocytes

J. Sandhu, M. Ribecco‐Lutkiewicz, A. Abulrob
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引用次数: 1

Abstract

Caveolae are plasma membrane invaginations that are enriched in cholesterol-binding proteins called caveolins. The presence of caveolae and caveolins in mixed cultures of human neurons and glia has not been investigated. Here, we sought to determine the presence of caveolae and caveolins in human NTera-2 (NT2/D1) cells, differentiated with retinoic acid into neuron-like (NT2/N) and astrocyte-like (NT2/A) cells. We found that while caveolin-3 mRNA levels remained relatively constant, caveolin-1 and -2 levels were upregulated in NT2/A and downregulated in NT2/N. No caveolin-1 immunoreactivity was detected in NT2/N. Electron microscopy revealed numerous flask-shaped invaginations (~86–102 nm in diameter) in the plasma membrane of NT2/A and NT2/N cells, while only few were detected in NT2/D1 cells. Immunoelectron microscopy localized caveolin-1 gold particles in the flask-shaped structures on plasmalemma and cytoplasmic vesicles of NT2/A cells. Furthermore, NT2/A endocytosed Alexa 488 conjugated-cholera toxin B subunit (CTX-B) through a caveolae- and clathrin-dependent pathway, whereas NT2/N endocytosed CTX-B through a caveolae-independent pathway. We have established that while NT2/A expressed functional caveolae, the molecular identity of the plasma membrane invaginations in NT2/N is unknown. The expression of caveolin proteins was differentially regulated in these cells. Taken together, our findings support the usefulness of the human NT2 model system to study the role of caveolins in neuron–glia communication, and their involvement in brain health and disease.
人NT-2神经元和星形胶质细胞混合培养小窝的分子和功能特征
小窝蛋白是质膜内陷,富含胆固醇结合蛋白,称为小窝蛋白。在人类神经元和神经胶质细胞的混合培养中,小窝和小窝蛋白的存在尚未得到研究。在这里,我们试图确定人NTera-2(NT2/D1)细胞中小窝和小窝蛋白的存在,该细胞用维甲酸分化为神经元样(NT2/N)和星形胶质细胞样(NT2/1)细胞。我们发现,虽然小窝蛋白-3 mRNA水平保持相对恒定,但小窝蛋白-1和-2水平在NT2/A中上调,在NT2/N中下调。在NT2/N中未检测到caveolin-1免疫反应性。电子显微镜显示,NT2/A和NT2/N细胞的质膜上有许多烧瓶状的凹陷(直径约86–102 nm),而在NT2/D1细胞中仅检测到少量凹陷。免疫电子显微镜将小窝蛋白-1金颗粒定位在NT2/A细胞质膜和细胞质小泡上的烧瓶状结构中。此外,NT2/A通过小窝和网格蛋白依赖性途径内吞Alexa 488偶联霍乱毒素B亚基(CTX-B),而NT2/N通过小窝非依赖性途径外吞CTX-B。我们已经证实,虽然NT2/A表达功能性小窝,但NT2/N中质膜内陷的分子身份尚不清楚。小窝蛋白的表达在这些细胞中受到不同的调节。总之,我们的发现支持了人类NT2模型系统在研究小窝蛋白在神经元-神经胶质细胞通讯中的作用及其与大脑健康和疾病的关系方面的有用性。
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