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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.

DOI:10.1002/ajh.2830200304
PMID:3877459
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。

相似文献

1
Granulopoiesis in patients with congenital neutropenia.先天性中性粒细胞减少症患者的粒细胞生成
Am J Hematol. 1985 Nov;20(3):223-34. doi: 10.1002/ajh.2830200304.
2
Granulopoiesis in severe congenital neutropenia.严重先天性中性粒细胞减少症中的粒细胞生成
Blood. 1976 Apr;47(4):531-8.
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Granulopoiesis in Shwachman's syndrome (pancreatic insufficiency and bone marrow dysfunction).施瓦赫曼综合征(胰腺功能不全和骨髓功能障碍)中的粒细胞生成
Pediatrics. 1979 Oct;64(4):515-9.
4
[Evaluation of granulopoiesis in congenital neutropenia (author's transl)].先天性中性粒细胞减少症中粒细胞生成的评估(作者译)
Rinsho Ketsueki. 1980 Sep;21(9):1342-8.
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Lithium therapy of children with chronic neutropenia.
Am J Med. 1981 May;70(5):1073-7. doi: 10.1016/0002-9343(81)90871-8.
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Alteration of colony-stimulating factor output, endotoxemia, and granulopoiesis in cyclic neutropenia.周期性中性粒细胞减少症中集落刺激因子输出、内毒素血症及粒细胞生成的改变
Am J Hematol. 1976;1(4):375-85. doi: 10.1002/ajh.2830010403.
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Stimulation of granulopoiesis by androgens without concomitant increase in the serum level of colony stimulating factor.
Exp Hematol. 1975 Jan;3(1):26-31.
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Granulopoietic precursors in chronic neutropenia.
Scand J Haematol. 1984 Nov;33(5):405-9. doi: 10.1111/j.1600-0609.1984.tb00717.x.
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The role of eosinophils in granulopoiesis. I. Eosinophilia in neutropenic patients.
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The inhibitory effect of circulating lymphocytes on granulopoiesis in human cyclic neutropenia in vitro.循环淋巴细胞对人周期性中性粒细胞减少症体外粒细胞生成的抑制作用。
Tohoku J Exp Med. 1984 Jun;143(2):213-20. doi: 10.1620/tjem.143.213.

引用本文的文献

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Reduction of CFU-GM and circulating hematopoietic progenitors in a subgroup of children with chronic neutropenia associated with severe infections and delayed recovery.慢性中性粒细胞减少症伴严重感染和恢复延迟的亚组患儿 CFU-GM 和循环造血祖细胞减少。
PLoS One. 2019 Mar 14;14(3):e0213782. doi: 10.1371/journal.pone.0213782. eCollection 2019.
2
A novel mutation in the juxtamembrane intracellular sequence of the granulocyte colony-stimulating factor (G-CSF) receptor gene in a patient with severe congenital neutropenia augments GCSF proliferation activity but not through the MAP kinase cascade.一名严重先天性中性粒细胞减少症患者的粒细胞集落刺激因子(G-CSF)受体基因近膜细胞内序列发生新型突变,增强了G-CSF的增殖活性,但并非通过丝裂原活化蛋白激酶(MAP)激酶级联反应。
Int J Hematol. 2005 Jul;82(1):28-34. doi: 10.1532/ijh97.05010.
3
Novel point mutation in the extracellular domain of the granulocyte colony-stimulating factor (G-CSF) receptor in a case of severe congenital neutropenia hyporesponsive to G-CSF treatment.一例对粒细胞集落刺激因子(G-CSF)治疗反应低下的严重先天性中性粒细胞减少症患者中,G-CSF受体细胞外结构域出现新的点突变。
J Exp Med. 1999 Aug 16;190(4):497-507. doi: 10.1084/jem.190.4.497.