Department of Comprehensive Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Pathology. 2013 Jun;45(4):408-16. doi: 10.1097/PAT.0b013e3283613dbf.
To determine the expression of CXCL12 in human spleens with extramedullary haematopoiesis (EMH) for clarifying the association of splenic haematopoietic stem cells (HSCs) with CXCL12, which has been demonstrated to be a marker of bone marrow niches.
We examined the expression of mRNA for CXCL12 by quantitative reverse transcription polymerase chain reaction (RT-PCR) and localised the CXCL12 protein by immunohistochemical staining in EMH negative and positive spleen samples from autopsy cases.
Expression of CXCL12 was significantly higher in samples from EMH positive cases than those from EMH negative cases. CXCL12 was localised to the endothelial cells of the sinuses of the red pulp in EMH positive spleens while vascular endothelial cells of the white pulp expressed CXCL12 throughout the spleen. c-kit positive/CD34 negative cells were identified in contact with CXCL12 positive endothelial cells of sinuses in EMH positive cases, although the number was few. In contrast, erythroblastic islands were frequently observed in EMH positive cases and dominantly localised to the intrasinusoidal spaces in association with CD68 positive macrophages.
Our results suggest that endothelial cells of splenic sinuses expressing CXCL12 may contribute to attracting circulating haematopoietic precursor cells and constitute bone marrow niche-like regions of EMH in humans. Differentiating haematopoietic cells may move into intrasinusoidal spaces to form EMH foci such as erythroblastic accumulation.
确定人脾脏中基质细胞衍生因子 1(SDF-1)/CXCL12 的表达,以阐明与骨髓龛相关的脾造血干细胞(HSCs),SDF-1/CXCL12 已被证明是骨髓龛的标志物。
我们通过定量逆转录聚合酶链反应(RT-PCR)检查了来自尸检的 EMH 阴性和阳性脾脏样本中 CXCL12 mRNA 的表达,并通过免疫组织化学染色定位了 CXCL12 蛋白。
EMH 阳性病例的 CXCL12 表达明显高于 EMH 阴性病例。CXCL12 定位于 EMH 阳性脾脏红髓窦内皮细胞,而白髓的血管内皮细胞在整个脾脏中表达 CXCL12。在 EMH 阳性病例中,c-kit 阳性/CD34 阴性细胞与 CXCL12 阳性窦内皮细胞接触,但数量较少。相比之下,EMH 阳性病例中经常观察到成红细胞岛,并且与 CD68 阳性巨噬细胞一起主要定位于窦内空间。
我们的结果表明,表达 CXCL12 的脾窦内皮细胞可能有助于吸引循环造血前体细胞,并构成人类 EMH 的骨髓龛样区域。分化的造血细胞可能进入窦内空间形成 EMH 灶,如成红细胞堆积。