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纤维连接蛋白抗体沿角膜基质胶原纤维的长度和周长原位标记,并在角膜后弹力层细胞和基质界面显示出明显的染色。

Fibronectin antibody labels corneal stromal collagen fibrils in situ along their length and circumference and demonstrates distinct staining along the cell and stromal interfaces of Descemet's membrane.

机构信息

Department of Biological Sciences, Oakland University , Rochester, MI , USA.

出版信息

Curr Eye Res. 2014 Mar;39(3):312-6. doi: 10.3109/02713683.2013.841260. Epub 2013 Oct 21.

Abstract

PURPOSE/AIM OF THE STUDY: An immunoperoxidase cytochemical study of fibronectin localization in the rat corneal stroma and Descemet's membrane was conducted following organ culture to determine whether stromal swelling allowed better primary antibody penetration into the normally tough fibrous corneal stroma.

MATERIALS AND METHODS

Following 24 h organ culture, corneas were fixed in 4% paraformaldehyde, washed and stained overnight at 4 °C in anti-fibronectin followed by washing and incubation in an appropriate secondary antibody and exposure to protein A-HRP. Cytochemical processing was carried out in a DAB-containing medium followed by dehydration and Epon embedding.

RESULTS

Observations of the stromal lamellae revealed the presence of a novel punctate staining pattern along the length of the collagen fibrils that extended around the fibril's circumference. Measurements on the peroxidase reaction product spacing indicated a periodicity of approximately 20.69 ± 3.57 nm along the fibril's length. Light microscopic immunocytochemistry revealed the presence of fibronectin staining occurred within the endothelial cell layer but only along the DM/stromal interface. Electron microscopic observations however, revealed that fibronectin staining occurred in distinct linear patterns along the length of both the endothelial and stromal DM interfaces.

DISCUSSION

Results indicate that organ culture mediated swelling helps facilitate the penetration of primary antibody into the corneal stroma. Observations suggest a novel association exists between fibronectin and stromal collagen fibrils that helps to mediate the arrangement and organization of the stromal extracellular matrix. Results also definitively indicate that fibronectin is deposited along both DM interfaces suggesting that it plays a role in the adhesion of both the endothelial cell layer and stroma to Descemet's membrane to help maintain the tissue architecture within this region of the cornea.

摘要

目的/研究目的:本研究通过器官培养对纤维连接蛋白在大鼠角膜基质和后弹力层中的定位进行免疫过氧化物酶细胞化学研究,以确定基质肿胀是否能使主要抗体更好地渗透到正常坚韧的纤维状角膜基质中。

材料和方法

器官培养 24 小时后,将角膜固定在 4%多聚甲醛中,在 4°C 下用抗纤维连接蛋白孵育过夜,然后洗涤并在适当的二级抗体中孵育,然后暴露于蛋白 A-HRP 中。细胞化学处理在含有 DAB 的培养基中进行,然后进行脱水和环氧树脂包埋。

结果

对基质层片的观察显示,在胶原纤维的长度上存在一种新的点状染色模式,这种模式沿着纤维的圆周延伸。对过氧化物酶反应产物间距的测量表明,纤维长度上的周期性约为 20.69±3.57nm。光镜免疫细胞化学显示,内皮细胞层内存在纤维连接蛋白染色,但仅存在于 DM/基质界面。然而,电子显微镜观察显示,纤维连接蛋白染色沿着内皮和基质 DM 界面的长度呈明显的线性模式。

讨论

结果表明,器官培养介导的肿胀有助于促进主要抗体渗透到角膜基质中。观察表明,纤维连接蛋白与基质胶原纤维之间存在一种新的关联,有助于调节基质细胞外基质的排列和组织。结果还明确表明,纤维连接蛋白沉积在两个 DM 界面上,表明它在维持角膜这一区域的组织结构方面发挥作用,有助于将内皮细胞层和基质粘附到后弹力层上。

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