Salamon A, Hámori J
Acta Morphol Acad Sci Hung. 1980;28(1-2):71-82.
In the contracting palmar aponeurosis of patients suffering from Dupuytren's disease myofibroblasts are revealed by electron microscopical examination. These cells display abnormal foldings of the nucleus, microfilaments resembling the myofilaments in smooth muscle cells, rough endoplasmic reticulum occupying circumscribed portions of the cytoplasm, free ribosomes, well-developed Golgi apparatus, numerous mitochondria, occasionally lipid droplets, cilia-like formations, hemidesmosomes and maculae adherens (desmosomes) between the cells and formation of basement membrane. According to literary data, the myofibroblasts contain actin and have contractile properties. These myofibroblasts are supposed to contribute to the development of Dupuytren's contracture. The process is finally stabilized by the disappearance of myofibroblasts and by the simultaneous development of compact collagenous fibre bundles secernated by classical fibroblasts.
在患有杜普伊特伦挛缩症患者的掌腱膜收缩组织中,通过电子显微镜检查发现了肌成纤维细胞。这些细胞呈现出细胞核的异常折叠、类似于平滑肌细胞中肌丝的微丝、占据细胞质特定部分的粗面内质网、游离核糖体、发达的高尔基体、大量线粒体、偶尔还有脂滴、纤毛样结构、半桥粒以及细胞间的黏着斑(桥粒),并形成基底膜。根据文献资料,肌成纤维细胞含有肌动蛋白并具有收缩特性。这些肌成纤维细胞被认为促使了杜普伊特伦挛缩的发展。该过程最终通过肌成纤维细胞的消失以及由典型成纤维细胞分泌的致密胶原纤维束的同时形成而得以稳定。