首页> 外文期刊>Ultrastructural pathology >The 'myofibroblast' that is omnipresent in pathology and key to the EMT concepts does not actually exist, since normal fibroblasts contain stress fibril organelles (SMA bundles with dense bodies) variably detected by TEM and IHC: Conclusions by a diagnostic pathologist with decades of ultrastructural experience
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The 'myofibroblast' that is omnipresent in pathology and key to the EMT concepts does not actually exist, since normal fibroblasts contain stress fibril organelles (SMA bundles with dense bodies) variably detected by TEM and IHC: Conclusions by a diagnostic pathologist with decades of ultrastructural experience

机译:实际上,病理学中无处不在的“肌成纤维细胞”和EMT概念的关键并不存在,因为正常的成纤维细胞含有应力原纤维细胞器(具有密集体的SMA束),可通过TEM和IHC进行检测:诊断病理学家的结论具有数十年的超微结构经验

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摘要

The so-called "enigmatic" unique "myofibroblast" has been erroneously substituted for virtually all things fibroblastic in soft tissue pathology and believed to be the ultimate fibrogenic cell. It is also internationally considered to be the mesenchymal cell in un-proven post-natal EMT, EMT organ/tissue fibrosis, and the assumption that EMT/MET is key to carcinoma/adenocarcinoma invasion and metastasis. However, no such cell exists, having been mistaken for our normal ubiquitous fibrogenic fibroblasts that contain peripheral bundles of actin (SMA) with dense bodies, i.e. stress fibril (SF) organelles variably detectable by TEM and SMA IHC, depending on the degree of activation. The only detectable features distinguishing what are erroneously believed to be two unique fibrogenic spindle cells are the SF. Is the variable detection of SF/SMA in fibroblastic and non-fibroblastic lesions significant? Carcinosarcomas are not bi-phasic malignancies or proof of EMT/MET. What does it mean that the fibroblasts of so-called "carcinoma-associated fibroblasts (CAF)" are not "myofibroblasts"? The true myofibroblast is the ultrastructurally and functionally unique, terminally-differentiated, pathognomonic cell of physiologic wound-healing, which unfortunately has been confused with the activated fibroblast. This study fails to demonstrate any ultrastructural evidence that either normal epithelial (EMT) or carcinoma/adenocarcinoma cells can undergo reversible transition into mesenchymal cells (EMT/MET) under any circumstances. The SF/SMA-positive fibrogenic cell in organ/tissue fibrosis is the genetically up-regulated, activated fibroblast, which has no relationship to EMT. Are any of the innumerable biochemical factors/elements considered to be associated with this non-existent cell and its related processes related to the activated fibroblast? The conclusions are based on review of every electron micrograph taken during a 40-year career in diagnostic and research ultrastructural pathology, and by confirming that the published TEM figures of so-called "myofibroblasts", are actually of fibroblasts.
机译:所谓的“神秘的”独特的“成肌纤维细胞”实际上已被软组织病理学上的成纤维细胞错误地替代,并被认为是最终的成纤维细胞。它在国际上也被认为是未经证实的产后EMT,EMT器官/组织纤维化的间充质细胞,并且认为EMT / MET是癌/腺癌侵袭和转移的关键。但是,没有这样的细胞存在,已经被误认为是我们的正常遍在纤维化成纤维细胞,其包含具有密集体的肌动蛋白(SMA)外围束,即根据激活程度可通过TEM和SMA IHC可变检测的应激原纤维(SF)细胞器。区分被错误认为是两个独特的纤维化纺锤体细胞的唯一可检测特征是SF。在成纤维细胞和非成纤维细胞病变中对SF / SMA的可变检测是否有意义?癌肉瘤不是双相性恶性肿瘤,也不是EMT / MET的证据。所谓的“癌相关成纤维细胞(CAF)”的成纤维细胞不是“肌成纤维细胞”是什么意思?真正的肌成纤维细胞是生理伤口愈合的超微结构和功能独特,终末分化的病理组织细胞,不幸的是,它已与活化的成纤维细胞相混淆。该研究未能证明任何超微结构证据表明正常上皮(EMT)或癌细胞/腺癌细胞在任何情况下均可经历可逆转变为间充质细胞(EMT / MET)。器官/组织纤维化中的SF / SMA阳性纤维化细胞是基因上调的活化成纤维细胞,与EMT无关。是否有无数的生化因素/元素被认为与此不存在的细胞及其相关过程有关,与活化的成纤维细胞有关?这些结论是基于对40年来从事诊断和研究超微结构病理学过程中所拍摄的每张电子显微照片的回顾,并通过证实所发表的所谓“成肌纤维细胞”的TEM图实际上是成纤维细胞而得出的。

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