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急性和慢性粒细胞白血病患者长期骨髓培养中基质微环境的缺陷

Defect of stromal microenvironment in long term bone marrow cultures of patients with acute and chronic myelogenous leukemias.

作者信息

Savchenko V G

机构信息

Department of Hematological Oncology and Bone Marrow Transplantation, Hematological Research Center, Moscow, Russia.

出版信息

Leuk Lymphoma. 1995 Sep;19(1-2):145-52. doi: 10.3109/10428199509059669.

Abstract

Inhibition of normal hemopoiesis is a regular finding in acute (AML) and chronic (CML) myelogenous leukemias and functional abnormalities of the hemopoietic microenvironment may be involved in this regard. In order to evaluate this possibility we studied the formation of adherent stromal cell layers (ASCL) in long term bone marrow cultures (LTBMC) of 7 patients with CML and 7 patients with AML and examined the ability of these ASCLs to support hemopoiesis after irradiation and a second inoculation of bone marrow cells. The formation of ASCLs was significantly impaired in CML and AML. These CML patients and 3 AML patients did not form typical ASCLs and the cellularity of these layers was greatly reduced. Colony forming unit granulocyte-macrophage (CFU-GM) production from bone marrow cells seeded on normal irradiated ASCLs peaked at week 3 and then gradually decreased by week 8. In CML and AML cocultures CFU-GM numbers decreased rapidly to zero by weeks 4-6 and did not differ significantly from the control cultures which did not contain preestablished ASCLs beginning from week 3. It is suggested that there may be a functional microenvironmental defect in CML and AML that may play a role in the pathogenesis of inhibition of normal hemopoiesis in these diseases.

摘要

正常造血功能受抑制是急性髓系白血病(AML)和慢性髓系白血病(CML)的常见表现,造血微环境的功能异常可能与此有关。为评估这种可能性,我们研究了7例CML患者和7例AML患者的长期骨髓培养(LTBMC)中贴壁基质细胞层(ASCL)的形成,并检测了这些ASCL在照射及再次接种骨髓细胞后支持造血的能力。CML和AML中ASCL的形成均显著受损。这些CML患者和3例AML患者未形成典型的ASCL,且这些细胞层的细胞数量大幅减少。接种于正常照射的ASCL上的骨髓细胞产生的集落形成单位粒细胞-巨噬细胞(CFU-GM)在第3周达到峰值,然后在第8周逐渐下降。在CML和AML共培养中,CFU-GM数量在第4 - 6周迅速降至零,从第3周开始与不含预先建立的ASCL的对照培养物相比无显著差异。提示CML和AML中可能存在功能性微环境缺陷,这可能在这些疾病中正常造血功能受抑制的发病机制中起作用。

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