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Ultrastructural analysis of mast cell recovery after secretion by piecemeal degranulation in B-cell non-Hodgkin's lymphoma.

机译:B细胞非霍奇金淋巴瘤通过零碎脱颗粒分泌后肥大细胞恢复的超微结构分析。

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摘要

Mast cells (MC) are critical for a number of pathological conditions, including acute and chronic inflammation and tumor angiogenesis. We have previously demonstrated in B-cell non-Hodgkin's lymphoma (B-NHL) the presence of an heterogeneous population of MC characterized by granules with a morphological semilunar appearance, or piecemeal partial degranulation (PMD), and containing scrolls. With the aim to further elucidate the morphological features of MC in B-NHL, in the present study an ultrastructural analysis of MC recovery after secretion by PMD in B-NHL samples has been carried out. Results indicate that PMD is identified by the presence of partially or completely empty granule containers in the cytoplasm, considered as the morphological endpoint of secretion by PMD. Granule refilling after PMD implies condensation of dense granule matrix material leading to the highly characteristics morphological patterns described in this paper. After the recovery from secretion by PMD in B-NHL, mature MC withfull complement of granules displaying crystal, particle, scroll, and mixed patterns are recognizable. We believe that the images presented here, in the absence of MC mitosis, support the possibility that in B-NHL, MC after PMD, refill empty granule containers in situ, as seen in MC during the angiogenic phase of wound-healing, and that both events, PMD and recovery of MC after their degranulation, occur during biological processes in which MC and angiogenesis are strictly interconnected.
机译:肥大细胞(MC)对于许多病理状况至关重要,包括急性和慢性炎症以及肿瘤血管生成。我们先前已经在B细胞非霍奇金淋巴瘤(B-NHL)中证实了MC异质种群的存在,其特征是具有形态半月形外观或零碎的部分脱粒(PMD)的颗粒,并且含有涡卷。为了进一步阐明B-NHL中MC的形态学特征,在本研究中,已进行了PMD分泌B-NHL样品后MC恢复的超微结构分析。结果表明,通过在细胞质中存在部分或完全空的颗粒容器来鉴定PMD,这被认为是PMD分泌的形态学终点。 PMD后的颗粒再填充意味着致密的颗粒基质材料的凝结,从而导致本文所述的高特征形态学模式。从B-NHL中的PMD分泌中恢复后,可以识别出成熟的MC,其中完整的颗粒互补,显示出晶体,颗粒,涡旋和混合模式。我们认为,此处呈现的图像在无MC有丝分裂的情况下,支持了在B-NHL,PMD后的MC中原位填充空的颗粒容器的可能性,如在伤口愈合的血管生成阶段在MC中所见, PMD和脱粒后MC的恢复这两个事件均发生在MC和血管生成严格相关的生物过程中。

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