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一种用于研究核基质热稳定性的联合超微结构方法。

A combined ultrastructural approach to the study of nuclear matrix thermal stabilization.

作者信息

Falcieri E, Gobbi P, Sabatelli P, Santi S, Farabegoli F, Rana R, Cataldi A, Maraldi N M, Martelli A M

机构信息

Istituto di Anatomia Umana Normale, Università di Bologna, Italy.

出版信息

Histochemistry. 1992 Sep;98(2):121-9. doi: 10.1007/BF00717003.

Abstract

Using mouse erythroleukaemia cells and different ultrastructural techniques, the morphology was investigated of the nuclear matrix obtained after incubation at 37 degrees C of isolated nuclei. If purified nuclei were heated for 45 min at 37 degrees C, the final matrix exhibited well-recognizable nucleolar remnants, an inner network and a peripheral lamina. Without such incubation only the peripheral lamina was seen surrounding homogeneous, finely granular material. Similar results were obtained with both araldite-embedded and freeze-fractured nuclear matrices, although in the latter case the loose granular material was not evident. Observations of araldite-embedded, heat-treated nuclei revealed clumping of heterochromatin in small, very electron-dense masses with large interchromatin spaces. These ultrastructural aspects were even more striking in freeze-fractured nuclei. Cytochemical matrix analysis by osmium-amine staining for nucleic acids and DNase-gold labelling for DNA localization demonstrated that also matrix residual nucleic acids, mostly RNA, are stabilized by heat exposure of isolated nuclei. The results demonstrate that the morphology of heat-stabilized nuclear matrix is not artefactually affected during the preparation for conventional electron microscopy and suggest a possible involvement of nucleic acids in the heat-induced stabilization of the nuclear matrix.

摘要

利用小鼠红白血病细胞和不同的超微结构技术,对分离的细胞核在37℃孵育后获得的核基质的形态进行了研究。如果将纯化的细胞核在37℃加热45分钟,最终的基质呈现出易于识别的核仁残余物、内部网络和周边层。未经这种孵育时,仅见周边层围绕着均匀的细颗粒物质。用环氧树脂包埋和冷冻断裂的核基质均得到了类似结果,不过在后一种情况下,松散的颗粒物质不明显。对环氧树脂包埋、热处理的细胞核的观察显示,异染色质聚集成小的、电子密度非常高的团块,染色质间空间很大。这些超微结构特征在冷冻断裂的细胞核中更为显著。通过锇胺染色进行核酸的细胞化学基质分析以及通过DNA酶-金标记进行DNA定位表明,分离细胞核的热暴露也能使基质残余核酸(主要是RNA)稳定下来。结果表明,热稳定核基质的形态在传统电子显微镜制备过程中不会受到人为影响,并提示核酸可能参与了热诱导的核基质稳定过程。

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