首页> 美国卫生研究院文献>Journal of Histochemistry and Cytochemistry >Subcellular Distribution and Relative Expression of Fibrocyte Markers in the CD/1 Mouse Cochlea Assessed by Semiquantitative Immunogold Electron Microscopy
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Subcellular Distribution and Relative Expression of Fibrocyte Markers in the CD/1 Mouse Cochlea Assessed by Semiquantitative Immunogold Electron Microscopy

机译:半定量免疫金电镜评估CD / 1小鼠耳蜗中纤维细胞标记物的亚细胞分布和相对表达

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摘要

Spiral ligament fibrocytes function in cochlear homeostasis, maintaining the endocochlear potential by participating in potassium recycling, and fibrocyte degeneration contributes to hearing loss. Their superficial location makes them amenable to replacement by cellular transplantation. Fibrocyte cultures offer one source of transplantable cells, but determining what fibrocyte types they contain and what phenotype transplanted cells may adopt is problematic. Here, we use immunogold electron microscopy to assess the relative expression of markers in native fibrocytes of the CD/1 mouse spiral ligament. Caldesmon and aquaporin 1 are expressed more in type III fibrocytes than any other type. S-100 is strongly expressed in types I, II, and V fibrocytes, and α1Na,K-ATPase is expressed strongly only in types II and V. By combining caldesmon or aquaporin 1 with S-100 and α1Na,K-ATPase, a ratiometric analysis of immunogold density distinguishes all except type II and type V fibrocytes. Other putative markers (creatine kinase BB and connective tissue growth factor) did not provide additional useful analytical attributes. By labeling serial sections or by double or triple labeling with combinations of three antibodies, this technique could be used to distinguish all except type II and type V fibrocytes in culture or after cellular transplantation into the lateral wall.
机译:螺旋韧带纤维细胞在耳蜗内稳态中起作用,通过参与钾的循环维持内耳蜗的潜力,而纤维细胞的变性会导致听力下降。它们的表面位置使其易于被细胞移植替代。纤维细胞培养物提供了可移植细胞的一种来源,但是要确定它们所包含的纤维细胞类型以及移植细胞可能采用的表型是有问题的。在这里,我们使用免疫金电子显微镜评估CD / 1小鼠螺旋韧带的天然纤维细胞中标记的相对表达。 Caldesmon和aquaporin 1在III型纤维细胞中的表达量高于其他任何类型。 S-100在I,II和V型纤维细胞中强烈表达,而α1Na,K-ATPase仅在II和V型中强烈表达。通过将caldesmon或水通道蛋白1与S-100和α1Na,K-ATPase结合,免疫金密度的比率分析可区分除II型和V型纤维细胞以外的所有纤维。其他推定标记(肌酸激酶BB和结缔组织生长因子)未提供其他有用的分析属性。通过标记连续切片或通过三种抗体的组合进行双重或三重标记,该技术可用于区分培养物中或细胞移植入侧壁后的所有除II型和V型纤维细胞。

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