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人提睾肌肌球蛋白同工型结构和表达的临床差异在隐睾和回缩睾丸中。

Clinically Differentiated Abnormalities of the Architecture and Expression of Myosin Isoforms of the Human Cremaster Muscle in Cryptorchidism and Retractile Testis.

机构信息

Division of Pediatric Surgery, Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Division of Pediatric Surgery, Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy,

出版信息

Urol Int. 2020;104(11-12):891-901. doi: 10.1159/000508432. Epub 2020 Jul 16.

Abstract

AIM

To describe architecture and expression of myosin isoforms of the human cremaster muscle (CM) and to individuate changes in clinically differentiated abnormalities of testicular descent: cryptorchidism or undescended testis (UDT) and retractile testis (RT).

BACKGROUND

The CM is a nonsomitic striated muscle differentiating from mesenchyme of the gubernaculum testis. Morphofunctional and molecular peculiarities linked to its unique embryological origin are not yet completely defined. Its role in abnormalities of testicular descent is being investigated.

SUBJECTS AND METHODS

Biopsy samples were obtained from corrective surgery in cases of cryptorchidism, retractile testis, inguinal hernia, or hydrocele. Muscle specimens were processed for morphology, histochemistry, and immunohistology.

RESULTS AND CONCLUSIONS

The CM differs from the skeletal muscles both for morphological and molecular characteristics. The presence of fascicles with different characterization and its myosinic pattern suggested that the CM could be included in the specialized muscle groups, such as the extrinsic ocular muscles (EOMs) and laryngeal and masticatory muscles. The embryological origin from the nonsomitic mesoderm is, also for the CM, the basis of distinct molecular pathways. In UDT, the histological alterations of CM are suggestive of denervation; the genitofemoral nerve and its molecular messengers directed to this muscle are likely defective. Compared with the other samples, RT has a distinct myosinic pattern; therefore, it has been considered a well-defined entity with respect to the other testicular descent abnormalities.

摘要

目的

描述人类提睾肌(CM)的肌球蛋白同工型的结构和表达,并确定临床上不同的睾丸下降异常(隐睾或未降睾丸(UDT)和回缩睾丸(RT))的变化。

背景

CM 是一种非体节横纹肌,从睾丸引带的间充质分化而来。与其独特的胚胎起源相关的形态功能和分子特征尚未完全定义。其在睾丸下降异常中的作用正在研究中。

受试者和方法

从隐睾、回缩睾丸、腹股沟疝或鞘膜积液的矫正手术中获得活检样本。肌肉标本进行形态学、组织化学和免疫组织化学处理。

结果和结论

CM 在形态和分子特征上与骨骼肌不同。不同特征的束的存在及其肌球蛋白模式表明,CM 可能属于特殊的肌肉群,如眼外肌(EOMs)、喉肌和咀嚼肌。非体节中胚层的胚胎起源也是 CM 独特分子途径的基础。在 UDT 中,CM 的组织学改变提示去神经支配;可能存在缺陷的是生殖股神经及其向该肌肉传递的分子信使。与其他样本相比,RT 具有明显不同的肌球蛋白模式;因此,与其他睾丸下降异常相比,它被认为是一种明确的实体。

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