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血小板需求调节骨髓中巨核细胞的血管内突出类型。

Platelet demand modulates the type of intravascular protrusion of megakaryocytes in bone marrow.

作者信息

Kowata Shugo, Isogai Sumio, Murai Kazunori, Ito Shigeki, Tohyama Koujiro, Ema Masatsugu, Hitomi Jiro, Ishida Yoji

机构信息

Yoji Ishida, Hematology and Oncology, Internal Medicine, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka, Iwate 020-8505, Japan, Tel.: +81 19 651 5111, Fax: +81 19 651 5185, E-mail:

出版信息

Thromb Haemost. 2014 Oct;112(4):743-56. doi: 10.1160/TH14-02-0123. Epub 2014 Jun 26.

Abstract

Megakaryocytes (MKs) generate platelets via intravascular protrusions termed proplatelets, which are tandem arrays of platelet-sized swellings with a beaded appearance. However, it remains unclear whether all intravascular protrusions in fact become proplatelets, and whether MKs generate platelets without forming proplatelets. Here, we visualised the sequential phases of intravascular MK protrusions and fragments in living mouse bone marrow (BM), using intravital microscopy, and examined their ultrastructure. The formation of intravascular protrusions was observed to be a highly dynamic process, in which the size and shape of the protrusions changed sequentially prior to the release of platelet progenitors. Among these intravascular protrusions, immature thick protrusions were distinguished from proplatelets by their size and the dynamic morphogenesis seen by time-lapse observation. In ultrastructural analyses, the thick protrusions and their fragments were characterised by a peripheral zone, abundant endoplasmic reticulum and demarcation membrane system, and random microtubule arrays. Proplatelets were predominant among BM sinusoids in the physiological state; however, during an acute thrombocytopenic period, thick protrusions increased markedly in the sinusoids. These results strongly suggested that BM MKs form and release two types of platelet progenitors via distinct intravascular protrusions, and that platelet demand modulates the type of intravascular protrusion that is formed in vivo.

摘要

巨核细胞(MKs)通过称为前血小板的血管内突起产生血小板,前血小板是呈串珠状外观的血小板大小的肿胀的串联阵列。然而,目前尚不清楚所有血管内突起是否实际上都变成了前血小板,以及巨核细胞是否在不形成前血小板的情况下产生血小板。在这里,我们使用活体显微镜观察了活小鼠骨髓(BM)中血管内巨核细胞突起和碎片的连续阶段,并检查了它们的超微结构。观察到血管内突起的形成是一个高度动态的过程,其中突起的大小和形状在血小板祖细胞释放之前会依次发生变化。在这些血管内突起中,未成熟的粗突起通过其大小和延时观察所见的动态形态发生与前血小板区分开来。在超微结构分析中,粗突起及其碎片的特征是有一个外周区、丰富的内质网和分界膜系统,以及随机的微管阵列。在生理状态下,前血小板在骨髓血窦中占主导地位;然而,在急性血小板减少期,血窦中的粗突起明显增加。这些结果有力地表明,骨髓巨核细胞通过不同的血管内突起形成并释放两种类型的血小板祖细胞,并且血小板需求调节体内形成的血管内突起的类型。

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