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心脏黏液瘤中表达胚胎非肌肉肌球蛋白重链的未成熟间充质细胞中的白细胞介素-6原位转录。

In situ interleukin-6 transcription in embryonic nonmuscle myosin heavy chain expressing immature mesenchyme cells of cardiac myxoma.

作者信息

Suzuki J, Takayama K, Mitsui F, Kono T, Yazaki Y, Takei M, Amano J, Isobe M

机构信息

First Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Cardiovasc Pathol. 2000 Jan-Feb;9(1):33-7. doi: 10.1016/s1054-8807(99)00031-9.

Abstract

Cardiac myxomas are benign tumors which sometimes secrete interleukin-6 (IL-6), however, the pathogenesis and the IL-6 secreting cells are not clear. There are vascular myosin heavy chain isoforms; SM2 expression is specific to mature smooth muscle cells, while SMemb is a nonmuscle-type isoform which is expressed in immature mesenchyme cells. We hypothesized that immature mesenchyme cells play pivotal roles in the secretion of IL-6; we studied these expression in resected samples of myxoma. SMemb expression was increased but SM2 expression was not in the channels of myxoma. Increased IL-6 transcription was observed in the SMemb expressing cells in the channel. Therefore, mesenchyme cells with immature phenotype in the channel play pivotal roles of inflammation and pathogenesis of cardiac myxoma.

摘要

心脏黏液瘤是有时会分泌白细胞介素-6(IL-6)的良性肿瘤,然而,其发病机制以及分泌IL-6的细胞尚不清楚。存在血管肌球蛋白重链异构体;SM2表达是成熟平滑肌细胞所特有的,而SMemb是一种非肌肉型异构体,在未成熟间充质细胞中表达。我们推测未成熟间充质细胞在IL-6的分泌中起关键作用;我们研究了这些表达在黏液瘤切除样本中的情况。在黏液瘤的通道中,SMemb表达增加但SM2表达未增加。在通道中表达SMemb的细胞中观察到IL-6转录增加。因此,通道中具有未成熟表型的间充质细胞在心脏黏液瘤的炎症和发病机制中起关键作用。

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