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先天性中性粒细胞减少症患者的粒细胞生成

Granulopoiesis in patients with congenital neutropenia.

作者信息

Kawaguchi Y, Kobayashi M, Tanabe A, Hara M, Nishi Y, Usui T, Nagai S, Nishibayashi Y, Nagao K, Yokoro K

出版信息

Am J Hematol. 1985 Nov;20(3):223-34. doi: 10.1002/ajh.2830200304.

Abstract

Granulopoiesis was investigated in five patients with congenital neutropenia (CN) (one Kostmann type, four benign forms). In semisolid agar culture, the marrow cells of all five patients produced normal numbers of CFU-c (colony-forming unit-culture). The size and classification of colonies were normal. In suspension culture in vitro with exogenous colony-stimulating factor (CSF) generated from omental-conditioned medium (OMCM), the myeloid precursors of all patients could proliferate and differentiate into normal polymorphonuclear neutrophils (PMNs). But in the absence of exogenous CSF, myeloid precursors of the patient with Kostmann-type CN did not proliferate or differentiate into PMNs at all. In the four patients with benign neutropenia, however, PMNs were found even without exogenous CSF similar to normal individuals. These results suggest that patients with CN may have normal granulopoietic stem cells with normal proliferative and differentiating capacity in response to exogenous CSF. When a small amount of normal human serum was added to normal marrow cultures stimulated by exogenous CSF, the colony growth increased in a superadditive manner. The enhancing activity of serum from neutropenic patients differed from that of normal serum. Especially, the addition of serum from the patient with Kostmann type CN to normal marrow cultures did not show this enhancement effect. The sera of patients with benign neutropenia had less enhancement effect than did normal control serum. These findings might be interpreted as showing an imbalance between CSF enhancer and inhibitors in the patients' serum.

摘要

对5例先天性中性粒细胞减少症(CN)患者(1例 Kostmann 型,4例良性型)的粒细胞生成情况进行了研究。在半固体琼脂培养中,所有5例患者的骨髓细胞产生的集落形成单位 - 培养物(CFU - c)数量正常。集落的大小和分类也正常。在体外与从网膜条件培养基(OMCM)产生的外源性集落刺激因子(CSF)进行悬浮培养时,所有患者的髓系前体细胞都能增殖并分化为正常的多形核中性粒细胞(PMN)。但在没有外源性CSF的情况下,Kostmann型CN患者的髓系前体细胞根本不增殖或分化为PMN。然而,在4例良性中性粒细胞减少症患者中,即使没有外源性CSF也能发现PMN,与正常个体相似。这些结果表明,CN患者可能具有正常的粒细胞生成干细胞,对外源性CSF具有正常的增殖和分化能力。当将少量正常人血清添加到由外源性CSF刺激的正常骨髓培养物中时,集落生长以超相加的方式增加。中性粒细胞减少症患者血清的增强活性与正常血清不同。特别是,将Kostmann型CN患者的血清添加到正常骨髓培养物中未显示出这种增强作用。良性中性粒细胞减少症患者的血清增强作用比正常对照血清小。这些发现可能被解释为表明患者血清中CSF增强剂和抑制剂之间存在失衡。

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