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血小板释放的一种糖蛋白对体外巨核细胞集落形成单位成熟的抑制作用

Suppression of maturation of megakaryocyte colony forming unit in vitro by a platelet-released glycoprotein.

作者信息

Dessypris E N, Gleaton J H, Sawyer S T, Armstrong O L

出版信息

J Cell Physiol. 1987 Mar;130(3):361-8. doi: 10.1002/jcp.1041300308.

Abstract

The suppressive role of platelets on the growth of human marrow megakaryocyte colony forming units (CFU-M) in vitro was investigated by the use of a plasma clot assay. An inverse correlation was established between the number of megakaryocytic colonies grown and the platelet concentration of the plasma or the resultant serum used in the culture system. The suppressive effect of platelets on megakaryocyte colony formation reached a plateau at normal human blood platelet concentration and was specific for CFU-M growth, since marrow cell erythroid burst formation (BFU-E) and granulocytic-monocytic colony formation (CFU-GM) remained unaffected. The inhibitory activity was detectable in the supernatants of platelet suspensions aggregated by thrombin or ADP, and the inhibitory activity released from ADP-stimulated platelets was blocked by pretreatment of platelets with monoclonal antibody HuPl-m1. Partial purification of this activity was achieved by diethylaminoethyl (DEAE)-ion exchange and phytohemagglutinin (PHA)-E agarose affinity chromatography. This inhibitor is a glycoprotein with a molecular weight of 12-17K daltons. This platelet released glycoprotein does not affect the early proliferative phase of CFU-M in vitro but acts on a day 6-8 CFU-M-derived cell by adversely affecting its maturation into recognizable megakaryocytes. These findings demonstrate that a glycoprotein released from platelets suppresses the maturation of CFU-M into megakaryocytes.

摘要

采用血浆凝块分析法研究了血小板在体外对人骨髓巨核细胞集落形成单位(CFU-M)生长的抑制作用。在培养系统中生长的巨核细胞集落数量与所用血浆或最终血清的血小板浓度之间建立了负相关关系。血小板对巨核细胞集落形成的抑制作用在正常人体血小板浓度时达到平台期,且对CFU-M生长具有特异性,因为骨髓细胞红系爆式集落形成(BFU-E)和粒系-单核系集落形成(CFU-GM)不受影响。在凝血酶或ADP聚集的血小板悬液上清液中可检测到抑制活性,用单克隆抗体HuPl-m1预处理血小板可阻断ADP刺激的血小板释放的抑制活性。通过二乙氨基乙基(DEAE)离子交换和植物血凝素(PHA)-E琼脂糖亲和层析对该活性进行了部分纯化。这种抑制剂是一种分子量为12 - 17千道尔顿的糖蛋白。这种血小板释放的糖蛋白在体外不影响CFU-M的早期增殖阶段,但在第6 - 8天作用于CFU-M衍生的细胞,通过不利地影响其成熟为可识别的巨核细胞。这些发现表明,血小板释放的一种糖蛋白可抑制CFU-M成熟为巨核细胞。

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