An ovine model for investigation of the microenvironment of the male mammary gland

IF 1.8 3区 医学 Q2 ANATOMY & MORPHOLOGY Journal of Anatomy Pub Date : 2024-05-12 DOI:10.1111/joa.14055
Benjamin P. Davies, Rachael C. Crew, Anna L. K. Cochrane, Katie Davies, André Figueiredo Baptista, Sonja Jeckel, Ian S. McCrone, Youguo Niu, Benjamin W. Strugnell, Katie Waine, Abigail L. Fowden, Clare E. Bryant, John W. Wills, Dino A. Giussani, Katherine Hughes
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Abstract

The specific biology of the male breast remains relatively unexplored in spite of the increasing global prevalence of male breast cancer. Delineation of the microenvironment of the male breast is restricted by the low availability of human samples and a lack of characterisation of appropriate animal models. Unlike the mouse, the male ovine gland persists postnatally. We suggest that the male ovine mammary gland constitutes a promising adjunctive model for the male breast. In this study, we evaluate the male ovine mammary gland microenvironment, comparing intact and neutered males. Assessment of the glandular histo-anatomy highlights the resemblance of the male gland to that of neonatal female sheep and confirms the presence of rudimentary terminal duct lobular units. Irrespective of neutered status, cell proliferation in epithelial and stromal compartments is similarly low in males, and cell proliferation in epithelial cells and in the intralobular stroma is significantly lower than in pubertal female sheep. Between 42% and 72% of the luminal mammary epithelial cells in the male gland express the androgen receptor and expression is significantly reduced by neutering. Luminal epithelial cells within the intact and neutered male gland also express oestrogen receptor alpha, but minimal progesterone receptor expression is observed. The distribution of leukocytes within the ducts and stroma is similar to the mammary gland of female sheep and females of other species. Both macrophages and T lymphocytes are intercalated in the epithelial bilayer and are more abundant in the intralobular stroma than the interlobular stroma, suggesting that they may have a protective immunological function within the vestigial glandular tissue of the male sheep. Mast cells are also observed within the stroma. These cells cluster near the glandular tissue and are frequently located adjacent to blood vessels. The abundance of mast cells is significantly higher in intact males compared to neutered males, suggesting that hormone signalling may impact mast cell recruitment. In this study, we demonstrate the utility of the male ovine mammary gland as a model for furthering our knowledge of postnatal male mammary biology.

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用于研究雄性乳腺微环境的绵羊模型。
尽管男性乳腺癌在全球的发病率越来越高,但男性乳房的特殊生物学特性仍相对缺乏研究。对男性乳腺微环境的研究受到了限制,因为人类样本很少,而且缺乏合适的动物模型。与小鼠不同,雄性绵羊的腺体在出生后仍然存在。我们认为雄性绵羊乳腺是一种很有前途的雄性乳腺辅助模型。在这项研究中,我们对雄性绵羊乳腺微环境进行了评估,并对完整的雄性绵羊和绝育的雄性绵羊进行了比较。对腺体组织解剖学的评估强调了雄性腺体与新生雌性绵羊腺体的相似性,并证实了末端导管小叶单元的存在。无论阉割与否,雄性绵羊上皮细胞和基质细胞的增殖率都很低,上皮细胞和小叶内基质细胞的增殖率明显低于青春期雌性绵羊。雄性腺体中 42% 到 72% 的管腔乳腺上皮细胞表达雄激素受体,而雄激素受体的表达因绝育而显著减少。完整和绝育的雄性乳腺管腔上皮细胞也表达雌激素受体α,但黄体酮受体表达极少。导管和基质中白细胞的分布与雌性绵羊和其他物种雌性绵羊的乳腺相似。巨噬细胞和 T 淋巴细胞都夹杂在上皮双层中,而且在小叶内基质中的含量比小叶间基质中的含量高,这表明它们在雄性绵羊的残余腺组织中可能具有保护性免疫功能。基质中还观察到肥大细胞。这些细胞聚集在腺组织附近,并经常位于血管附近。与阉割雄性绵羊相比,完整雄性绵羊的肥大细胞丰度明显更高,这表明激素信号可能会影响肥大细胞的招募。在这项研究中,我们证明了雄性绵羊乳腺作为模型的实用性,有助于我们进一步了解出生后雄性乳腺生物学。
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来源期刊
Journal of Anatomy
Journal of Anatomy 医学-解剖学与形态学
CiteScore
4.80
自引率
8.30%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Journal of Anatomy is an international peer-reviewed journal sponsored by the Anatomical Society. The journal publishes original papers, invited review articles and book reviews. Its main focus is to understand anatomy through an analysis of structure, function, development and evolution. Priority will be given to studies of that clearly articulate their relevance to the anatomical community. Focal areas include: experimental studies, contributions based on molecular and cell biology and on the application of modern imaging techniques and papers with novel methods or synthetic perspective on an anatomical system. Studies that are essentially descriptive anatomy are appropriate only if they communicate clearly a broader functional or evolutionary significance. You must clearly state the broader implications of your work in the abstract. We particularly welcome submissions in the following areas: Cell biology and tissue architecture Comparative functional morphology Developmental biology Evolutionary developmental biology Evolutionary morphology Functional human anatomy Integrative vertebrate paleontology Methodological innovations in anatomical research Musculoskeletal system Neuroanatomy and neurodegeneration Significant advances in anatomical education.
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