Department of Anatomy, Diagnostic Pathology, Forensic Medicine, Hygiene and Public Health, University of Catania, Italy.
J Sex Med. 2011 Jan;8(1):109-15. doi: 10.1111/j.1743-6109.2010.02003.x. Epub 2010 Sep 14.
Peyronie's disease (PD) is a connective tissue disorder of tunica albuginea (TA), a thick fibrous sheath surrounding the corpora cavernosa of the penis. Relatively, little is known about the disease itself.
To investigate whether the apoptosis cascade in degenerated and macroscopically deformed TA from men with PD is activated through the extrinsic pathway, by assessing the immunoexpression of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and its death receptor, DR5.
TA plaques from 15 men with PD and from four unaffected men were processed for TRAIL and DR5 immunohistochemistry and Western blot analysis.
A greater understanding of the pathophysiology of PD through a molecular approach, to gain insights that may lead to novel forms of treatment.
Activation of the apoptosis mechanisms through the extrinsic pathway was demonstrated by TRAIL and DR5 overexpression in fibroblasts and myofibroblasts from affected TA.
The finding that apoptosis activation in TA plaques occurs, at least in part, via the extrinsic pathway may help devise novel therapeutic options for these patients.
佩罗尼氏病(PD)是一种阴茎海绵体白膜(TA)的结缔组织疾病,白膜是一种包裹阴茎海绵体的厚纤维鞘。相对而言,人们对这种疾病本身知之甚少。
通过评估肿瘤坏死因子相关凋亡诱导配体(TRAIL)及其死亡受体 DR5 的免疫表达,研究 PD 患者退变和宏观变形的 TA 中凋亡级联是否通过外在途径激活。
对 15 名 PD 男性和 4 名未受影响男性的 TA 斑块进行 TRAIL 和 DR5 免疫组织化学和 Western blot 分析。
通过分子方法更深入地了解 PD 的病理生理学,以获得可能导致新治疗形式的见解。
受影响的 TA 中的成纤维细胞和肌成纤维细胞中 TRAIL 和 DR5 的过度表达表明,通过外在途径激活了凋亡机制。
TA 斑块中凋亡的激活至少部分是通过外在途径发生的,这可能有助于为这些患者设计新的治疗选择。