Ivanova Elena, Toychiev Abduqodir H, Yee Christopher W, Sagdullaev Botir T
Ophthalmology, Weill Medical College of Cornell University.
J Vis Exp. 2013 Dec 13(82):e51018. doi: 10.3791/51018.
Working with delicate tissue can be a complicating factor when performing immunohistochemical assessment. Here, we present a method that utilizes a ring-supported hydrophilized PTFE membrane to provide structural support to both living and fixed tissue during immunohistochemical processing, which allows for the use of a variety of protocols that would otherwise cause damage to the tissue. First, this is demonstrated with bolus loading of fluorescent markers into living retinal tissue. This method allows for quick visualization of targeted structures, while the membrane support maintains tissue integrity during the injection and allows for easy transfer of the preparation for further imaging or processing. Second, a procedure for antibody staining in tissue fixed with carbodiimide is described. Though paraformaldehyde fixation is more common, carbodiimide fixation provides a superior substrate for the visualization of synaptic proteins. A limitation of carbodiimide is that the resulting fixed tissue is relatively fragile; however, this is overcome with the use of the supporting membrane. Retinal tissue is used to demonstrate these techniques, but they may be applied to any fragile tissue.
在进行免疫组织化学评估时,处理 delicate 组织可能是一个复杂因素。在此,我们提出一种方法,该方法利用环形支撑的亲水化聚四氟乙烯膜在免疫组织化学处理过程中为活体和固定组织提供结构支撑,这使得能够使用各种否则会对组织造成损害的方案。首先,通过将荧光标记物大剂量注入活体视网膜组织来证明这一点。该方法允许快速可视化目标结构,而膜支撑在注射过程中保持组织完整性,并便于将制剂转移以便进一步成像或处理。其次,描述了在经碳二亚胺固定的组织中进行抗体染色的程序。虽然多聚甲醛固定更为常见,但碳二亚胺固定为突触蛋白的可视化提供了更好的底物。碳二亚胺的一个局限性是所得固定组织相对脆弱;然而,通过使用支撑膜可以克服这一问题。视网膜组织用于演示这些技术,但它们可应用于任何脆弱组织。