Flake Gordon P, Moore Alicia B, Sutton Deloris, Kissling Grace E, Horton John, Wicker Benita, Walmer David, Robboy Stanley J, Dixon Darlene
Cellular and Molecular Pathology Branch, National Toxicology Program (NTP), National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), Department of Health and Human Services, Research Triangle Park, NC 27709, USA.
Molecular Pathogenesis Group, National Toxicology Program Laboratory (NTPL), National Toxicology Program (NTP), National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), Department of Health and Human Services, Research Triangle Park, NC 27709, USA.
Obstet Gynecol Int. 2013;2013:528376. doi: 10.1155/2013/528376. Epub 2013 Nov 21.
We propose, and offer evidence to support, the concept that many uterine leiomyomas pursue a self-limited life cycle. This cycle can be arbitrarily divided on the basis of morphologic assessment of the collagen content into 4 phases: (1) proliferation, (2) proliferation and synthesis of collagen, (3) proliferation, synthesis of collagen, and early senescence, and (4) involution. Involution occurs as a result of both vascular and interstitial ischemia. Interstitial ischemia is the consequence of the excessive elaboration of collagen, resulting in reduced microvascular density, increased distance between myocytes and capillaries, nutritional deprivation, and myocyte atrophy. The end stage of this process is an involuted tumor with a predominance of collagen, little to no proliferative activity, myocyte atrophy, and myocyte cell death. Since many of the dying cells exhibit light microscopic and ultrastructural features that appear distinct from either necrosis or apoptosis, we refer to this process as inanosis, because it appears that nutritional deprivation, or inanition, is the underlying cause of cell death. The disposal of myocytes dying by inanosis also differs in that there is no phagocytic reaction, but rather an apparent dissolution of the cell, which might be viewed as a process of reclamation as the molecular contents are reclaimed and recycled.
我们提出并提供证据支持这样一种概念,即许多子宫平滑肌瘤具有自我限制的生命周期。基于对胶原蛋白含量的形态学评估,这个周期可被任意划分为4个阶段:(1)增殖期,(2)增殖与胶原蛋白合成期,(3)增殖、胶原蛋白合成与早期衰老期,以及(4)退化期。退化是血管和间质缺血共同作用的结果。间质缺血是胶原蛋白过度分泌的后果,导致微血管密度降低、肌细胞与毛细血管之间的距离增加、营养缺乏以及肌细胞萎缩。这个过程的末期是一个退化的肿瘤,以胶原蛋白为主,增殖活性很少或没有,肌细胞萎缩,肌细胞死亡。由于许多死亡细胞呈现出在光学显微镜和超微结构上与坏死或凋亡均不同的特征,我们将这个过程称为细胞营养耗竭,因为似乎营养缺乏,即营养耗竭,是细胞死亡的根本原因。因细胞营养耗竭而死亡的肌细胞的处理方式也有所不同,即不存在吞噬反应,而是细胞明显溶解,这可能被视为一种回收过程,因为分子成分被回收和再利用。