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Ultrastructural analysis of the development of human basophils and mast cells in vitro

机译:体外人类嗜碱性粒细胞和肥大细胞发育的超微结构分析

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The ultrastructural analysis of a variety of culture systems of human cord blood mononuclear cells (spanning a 10-year research effort) is reviewed. Human basophils, eosinophils and mast cells reliably developed from their agranular precursors that are present in human cord blood. Suspension cultures and cocultures with fibroblasts were used to examine the effects on differentiation and maturation of full (fibroblast), interleukin-2-depleted (human T cells), and murine inducer T cell culture supernatants, partially purified mouse fibroblast factor(s), recombinant human interleukins 3 and 5, and recombinant human and murine c-kit ligands (stem cell factor, mast cell growth factor). Together, these studies allowed us to define the differentiation and full maturation of the basophil and eosinophil lineages and provided evidence for the induction of a form of secretion (termed piecemeal degranulation) of the basophil and eosinophil lineages in interleukin-3- or-5-supplemented cultures. Mast cells were absent from interleukin-3- or-5-containing cultures. The development of fully mature mast cells occurred regularly in fibroblast-containing cocultures; partially mature mast cells developed in fibroblast culture supernatant-, partially purified mouse fibroblast factors(s)-, and either recombinant human or murine c-kit ligand-supplemented suspension cultures. Small numbers of basophils and eosinophils were present in the suspension cultures the received c-kit ligand in its recombinant or naturally occurring forms. Ultrastructural immunogold analyses confirmed that basophils and eosinophils contained the Charcot-Leyden crystal protein (in different subcellular locations) but that mast cells did not. In both cocultures and suspension cultures, the primary event recorded for mast cells was that of differentiation and maturation, with the ultrastructural correlates of synthetic activity and granule building prevailing. Spontaneous secretory events, recognizable by ultrastructural analysis, were not evident, in either mature or partially mature mast cells developing in these cultures.
机译:回顾了人脐带血单核细胞各种培养系统的超微结构分析(跨越 10 年的研究工作)。人类嗜碱性粒细胞、嗜酸性粒细胞和肥大细胞可靠地从存在于人类脐带血中的颗粒前体发育而来。使用悬浮培养物和与成纤维细胞共培养来检查全(成纤维细胞)、白细胞介素-2 耗尽(人 T 细胞)和小鼠诱导剂 T 细胞培养上清液、部分纯化的小鼠成纤维细胞因子、重组人白细胞介素 3 和 5 以及重组人和小鼠 c-kit 配体(干细胞因子、肥大细胞生长因子)对分化和成熟的影响。总之,这些研究使我们能够确定嗜碱性和嗜酸性粒细胞谱系的分化和完全成熟,并为在白细胞介素-3 或 5 补充培养物中诱导嗜碱性和嗜酸性粒细胞谱系的一种分泌形式(称为零碎脱颗粒)提供了证据。含有白细胞介素 3 或 5 的培养物中不存在肥大细胞。完全成熟的肥大细胞的发育在含有成纤维细胞的共培养物中定期发生;在成纤维细胞培养上清液、部分纯化的小鼠成纤维细胞因子以及重组人或小鼠 C-Kit 配体补充的悬浮培养物中发育的部分成熟肥大细胞。少量嗜碱性粒细胞和嗜酸性粒细胞存在于悬浮培养物中,接受的c-kit配体以重组或天然形式存在。超微结构免疫金分析证实,嗜碱性粒细胞和嗜酸性粒细胞含有Charcot-Leyden晶体蛋白(在不同的亚细胞位置),但肥大细胞没有。在共培养和悬浮培养中,肥大细胞记录的主要事件是分化和成熟,合成活性和颗粒构建的超微结构相关性占主导地位。通过超微结构分析可识别的自发分泌事件在这些培养物中发育的成熟或部分成熟的肥大细胞中并不明显。

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