Rinaldi Vera D, Bloom Jordana C, Schimenti John C
Department of Biomedical Sciences, Cornell University;
Department of Molecular Biology and Genetics, Cornell University.
J Vis Exp. 2018 May 2(135):57593. doi: 10.3791/57593.
Research in the field of mammalian reproductive biology often involves evaluating the overall health of ovaries and testes. Specifically, in females, ovarian fitness is often assessed by visualizing and quantifying follicles and oocytes. Because the ovary is an opaque three-dimensional tissue, traditional approaches require laboriously slicing the tissue into numerous serial sections in order to visualize cells throughout the entire organ. Furthermore, because quantification by this method typically entails scoring only a subset of the sections separated by the approximate diameter of an oocyte, it is prone to inaccuracy. Here, a protocol is described that instead utilizes whole organ tissue clearing and immunofluorescence staining of mouse ovaries to visualize follicles and oocytes. Compared to more traditional approaches, this protocol is advantageous for visualizing cells within the ovary for numerous reasons: 1) the ovary remains intact throughout sample preparation and processing; 2) small ovaries, which are difficult to section, can be examined with ease; 3) cellular quantification is more readily and accurately achieved; and 4) the whole organ imaged.
哺乳动物生殖生物学领域的研究通常涉及评估卵巢和睾丸的整体健康状况。具体而言,对于雌性动物,卵巢健康状况通常通过观察和量化卵泡及卵母细胞来评估。由于卵巢是一种不透明的三维组织,传统方法需要费力地将组织切成许多连续切片,以便观察整个器官中的细胞。此外,由于通过这种方法进行量化通常只需要对间隔约为一个卵母细胞直径的部分切片进行评分,因此容易出现不准确的情况。在此,我们描述了一种方案,该方案利用小鼠卵巢的全器官组织透明化和免疫荧光染色来观察卵泡和卵母细胞。与更传统的方法相比,该方案在观察卵巢内细胞方面具有诸多优势:1)在整个样品制备和处理过程中卵巢保持完整;2)难以切片的小卵巢可以轻松检查;3)细胞量化更容易且更准确地实现;4)对整个器官进行成像。