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淋巴结细胞培养物免疫后肥大细胞的分化与活性

Differentiation and activity of mast cells following immunization in cultures of lymph-node cells.

作者信息

Ginsburg H, Nir I, Hammel I, Eren R, Weissman B A, Naot Y

出版信息

Immunology. 1978 Sep;35(3):485-502.

Abstract

An extensive clonal differentiation into mast cells from primitive blast cell precursors occurred when lymph node cells obtained from mice immunized with horse serum were cultured on mouse embryonic skin monolayers. Horse serum was always present in the culture as a constituent of the nutritional medium. Mast cells developed to lesser extent also in cultures prepared from non-immunized mice. However, a clear difference in mast cell-granule ultrastructure and in histamine content was noted between the two. In cultures of lymph nodes cells from non-immunized mice the granules were tiny and uniform in size and in staining density; whereas granules in the immune cultures were larger and non-uniform in size and in staining density, and the intragranular organization manifested alterations of various forms. The content of intracellular histamine per 10(6) mast cells was about equal in both cultures. However, much more free histamine (per 10(6) mast cells) gradually accumulated in cultures of the immune lymph node cells, indicating higher rates of synthesis and release of histamine. The mast cells were readily degranulated by heat-inactivated (IgG1) sera of the mice used as donors of the lymph node cells. 92% of the mast cells were degranulated and as much as 80% of the histamine was released. The degranulation was accompanied by an immediate (albeit reversible) response of the fibroblast cells in the monolayer. A shift of the well-stretched cytoplasm of the fibroblasts opened numerous 'window' over the whole monolayer. The degranulated mast cells survived the process and could be maintained further in the cultures. Moreover, they were capable of repeated degranulation, releasing 50% of their histamine, even after four degranulation cycles performed over a 7 days' period of culture. No cytotoxic effect on the mast cells was noted and the histamine content in culture, 3 days after degranulation, seemed to be higher than in the undergranulated control cultures--suggesting an intensified rate of histamine synthesis.

摘要

当将用马血清免疫的小鼠的淋巴结细胞接种于小鼠胚胎皮肤单层上培养时,原始母细胞前体可广泛克隆分化为肥大细胞。培养过程中,马血清作为营养培养基的成分始终存在。未免疫小鼠制备的培养物中也会有程度较轻的肥大细胞发育。然而,两者之间在肥大细胞颗粒超微结构和组胺含量方面存在明显差异。未免疫小鼠的淋巴结细胞培养物中,颗粒微小,大小和染色密度均一;而免疫培养物中的颗粒更大,大小和染色密度不均一,颗粒内结构呈现多种形式的改变。两种培养物中每10⁶个肥大细胞的细胞内组胺含量大致相等。然而,免疫淋巴结细胞培养物中逐渐积累了更多的游离组胺(每10⁶个肥大细胞),表明组胺的合成和释放速率更高。肥大细胞很容易被用作淋巴结细胞供体的小鼠的热灭活(IgG1)血清脱颗粒。92%的肥大细胞发生脱颗粒,释放了高达80%的组胺。脱颗粒伴随着单层中纤维母细胞的即时(尽管是可逆的)反应。纤维母细胞伸展良好的细胞质发生移位,在整个单层上打开了许多“窗口”。脱颗粒的肥大细胞在此过程中存活下来,并可在培养物中进一步维持。此外,即使在7天的培养期内进行了4次脱颗粒循环后,它们仍能够反复脱颗粒,释放其50%的组胺。未观察到对肥大细胞的细胞毒性作用,脱颗粒3天后培养物中的组胺含量似乎高于颗粒较少的对照培养物,这表明组胺合成速率加快。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b2e/1457637/c31f90235353/immunology00272-0059-a.jpg

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