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使用平滑肌肌球蛋白重链作为滤泡树突状细胞的有效标志物。

Use of Smooth Muscle Myosin Heavy Chain as an Effective Marker of Follicular Dendritic Cells.

作者信息

Ioannidis Ioannis, Laurini Javier A

机构信息

Department of Pathology, Pennsylvania Hospital (University of Pennsylvania Health System), Philadelphia, PA.

Department of Pathology, University of South Alabama Medical Center, Mobile, AL.

出版信息

Appl Immunohistochem Mol Morphol. 2019 Jan;27(1):48-53. doi: 10.1097/PAI.0000000000000538.

Abstract

Smooth muscle myosin heavy chain (SMMHC) is a major structural component of the contractile apparatus in smooth muscle cells. Even though it is considered a relatively specific marker for terminal smooth muscle cell differentiation, expression in other cell types such as follicular dendritic cells (FDCs) has rarely been reported. To determine whether SMMHC represents an effective FDC marker in lymphoid tissues, we compared the immunohistochemical results for SMMHC with those of the traditional FDC markers podoplanin (D2-40) and CD21. Paraffin sections of 44 lymphoid tissues were analyzed, including 31 cases of follicular hyperplasia, 6 cases of follicular lymphoma, 2 cases of peripheral T-cell lymphoma, 3 cases of diffuse large B-cell lymphoma arising in follicular lymphoma, 1 case of nodular sclerosis classical Hodgkin lymphoma, and 1 case of small lymphocytic lymphoma. There was no statistically significant difference between the number of SMMHC-positive and D2-40-positive or CD21 lymph nodes (P>0.05). The extent and intensity of SMMHC-positive FDCs were similar to those of D2-40-positive FDCs (P=0.127 and 0.733, respectively), but significantly lower compared with those of CD21 cells (P=0.009 and 0.00002, respectively). However, in contrast to CD21 which was also positive in some germinal center B cells, SMMHC expression was restricted to FDCs. Our results indicate that SMMHC is an excellent marker for FDCs and can be particularly helpful in demonstrating the underlying architecture in lymphoid processes.

摘要

平滑肌肌球蛋白重链(SMMHC)是平滑肌细胞收缩装置的主要结构成分。尽管它被认为是终末平滑肌细胞分化的相对特异性标志物,但在其他细胞类型如滤泡树突状细胞(FDC)中的表达鲜有报道。为了确定SMMHC是否是淋巴组织中有效的FDC标志物,我们将SMMHC的免疫组化结果与传统FDC标志物血小板内皮细胞黏附分子(D2-40)和CD21的结果进行了比较。分析了44个淋巴组织的石蜡切片,包括31例滤泡增生、6例滤泡性淋巴瘤、2例外周T细胞淋巴瘤、3例由滤泡性淋巴瘤演变而来的弥漫性大B细胞淋巴瘤、1例结节硬化型经典霍奇金淋巴瘤和1例小淋巴细胞淋巴瘤。SMMHC阳性淋巴结与D2-40阳性或CD21阳性淋巴结的数量之间无统计学显著差异(P>0.05)。SMMHC阳性FDC的范围和强度与D2-40阳性FDC相似(分别为P=0.127和0.733),但与CD21细胞相比显著更低(分别为P=0.009和0.00002)。然而,与在一些生发中心B细胞中也呈阳性的CD21不同,SMMHC表达仅限于FDC。我们的结果表明,SMMHC是FDC的优良标志物,在显示淋巴过程的潜在结构方面可能特别有帮助。

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