原发性(特发性)骨髓纤维化的脾造血:免疫组织化学和形态计量学评价红细胞增殖活性和巨核造血的内复制能力(PCNA-和Ki-67染色)。

J Thiele, F G Bennewitz, H P Bertsch, S Falk, R Fischer, H J Stutte
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引用次数: 9

摘要

使用抗增殖细胞核抗原或PCNA (PC10)和Ki-67抗原(MIB1)的单克隆抗体,对10例原发性(特发性)骨髓性纤维化(OMF)患者常规处理的脾组织进行了免疫组织化学和形态计量学研究。为了测定红细胞前体的增殖能力和巨核细胞的内复制活性,将相应的抗体(Ret40f和CD61)与细胞周期标记物(顺序双免疫染色)联合使用。形态计量学分析显示两种细胞系的PCNA和Ki-67反应性无显著差异。与以往对正常骨髓的研究相比,在骨髓化生的脾组织中,pcna标记的原红母细胞、红母细胞和巨核细胞数量明显增加。考虑到OMF中红细胞的无效生成,红细胞系的PCNA和Ki-67免疫染色似乎有不成比例的增强。同样,晚期巨核细胞的小尺寸,omf相关的骨髓化生与内复制活性的损害保持一致。除了各种其他促成因素外,OMF中的贫血可能部分由继发性叶酸(血液)缺乏引起。从实验研究中,已知这种缺陷会导致细胞周期s期的异常停止,与恶性贫血的特征相当。作为这种病理机制的后续,必须假设PCNA和Ki-67的过度表达,这并不一定与DNA合成或细胞周期相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Splenic haematopoiesis in primary (idiopathic) osteomyelofibrosis: immunohistochemical and morphometric evaluation of proliferative activity of erytro- and endoreduplicative capacity of megakaryopoiesis (PCNA- and Ki-67 staining).

Using monoclonal antibodies against proliferating cell nuclear antigen or PCNA (PC10) and the Ki-67 antigen (MIB1), an immunohistochemical and morphometric study was performed on routinely processed splenic tissue from ten patients with primary (idiopathic) osteomyelofibrosis (OMF). To determine the proliferation capacity of erythroid precursors and the endoreduplicative activity of megakaryocytes, corresponding antibodies (Ret40f and CD61) were applied in combination with the cell-cycle markers (sequential double-immunostaining). Morphometric analysis revealed no significant differences in PCNA or Ki-67 reactivity in either cell lineages. In comparison with previous studies on normal bone marrow, in splenic tissue showing myeloid metaplasia, the numbers of PCNA-labelled proerythroblasts, erythroblasts and megakaryocytes were conspicuously increased. Considering the ineffective erythropoiesis in OMF, there seemed to be a disproportional enhancement in PCNA and Ki-67 immunostaining of the red cell lineage. Similarly, the small size of megakaryocytes in advanced, OMF-associated myeloid metaplasia was in keeping with an impairment of endoreduplicative activity. In addition to various other contributory factors, anaemia in OMF may be partially caused by secondary folate (haematinic) deficiency. From experimental studies this defect is known to cause an abnormal arrest in the S-phase of the cell-cycle, comparable to that characterising pernicious anaemia. As a sequel of this pathomechanism, an undue overexpression of PCNA and Ki-67 has to be assumed, that is not necessarily associated with DNA synthesis or cell cycling.

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