Georgas Kylie M, Armstrong Jane, Keast Janet R, Larkins Christine E, McHugh Kirk M, Southard-Smith E Michelle, Cohn Martin J, Batourina Ekatherina, Dan Hanbin, Schneider Kerry, Buehler Dennis P, Wiese Carrie B, Brennan Jane, Davies Jamie A, Harding Simon D, Baldock Richard A, Little Melissa H, Vezina Chad M, Mendelsohn Cathy
Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland 4072, Australia.
Center for Integrative Physiology, University of Edinburgh, Edinburgh EH8 9XD, UK.
Development. 2015 May 15;142(10):1893-908. doi: 10.1242/dev.117903. Epub 2015 May 12.
Malformation of the urogenital tract represents a considerable paediatric burden, with many defects affecting the lower urinary tract (LUT), genital tubercle and associated structures. Understanding the molecular basis of such defects frequently draws on murine models. However, human anatomical terms do not always superimpose on the mouse, and the lack of accurate and standardised nomenclature is hampering the utility of such animal models. We previously developed an anatomical ontology for the murine urogenital system. Here, we present a comprehensive update of this ontology pertaining to mouse LUT, genital tubercle and associated reproductive structures (E10.5 to adult). Ontology changes were based on recently published insights into the cellular and gross anatomy of these structures, and on new analyses of epithelial cell types present in the pelvic urethra and regions of the bladder. Ontology changes include new structures, tissue layers and cell types within the LUT, external genitalia and lower reproductive structures. Representative illustrations, detailed text descriptions and molecular markers that selectively label muscle, nerves/ganglia and epithelia of the lower urogenital system are also presented. The revised ontology will be an important tool for researchers studying urogenital development/malformation in mouse models and will improve our capacity to appropriately interpret these with respect to the human situation.
泌尿生殖道畸形给儿科带来了相当大的负担,许多缺陷影响下尿路(LUT)、生殖结节及相关结构。对这类缺陷分子基础的理解常常借助小鼠模型。然而,人体解剖学术语并不总是能直接套用到小鼠身上,缺乏准确和标准化的命名法正阻碍着此类动物模型的应用。我们之前为小鼠泌尿生殖系统开发了一个解剖本体论。在此,我们展示了该本体论关于小鼠下尿路、生殖结节及相关生殖结构(胚胎第10.5天至成年期)的全面更新。本体论的变化基于近期发表的对这些结构细胞和大体解剖学的见解,以及对盆腔尿道和膀胱区域存在的上皮细胞类型的新分析。本体论的变化包括下尿路、外生殖器和下部生殖结构内的新结构、组织层和细胞类型。还展示了代表性插图、详细的文字描述以及选择性标记下泌尿生殖系统肌肉、神经/神经节和上皮的分子标记。修订后的本体论将成为研究小鼠模型中泌尿生殖发育/畸形的研究人员的重要工具,并将提高我们根据人类情况对其进行适当解读的能力。