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造血祖细胞:嗜酸性粒细胞/嗜碱性粒细胞祖细胞在过敏性气道炎症中的作用。

Hemopoietic progenitors: the role of eosinophil/basophil progenitors in allergic airway inflammation.

机构信息

Department of Medicine, McMaster University, Hamilton, ON L8N 3Z5, Canada.

出版信息

Expert Rev Clin Immunol. 2005 May;1(1):87-101. doi: 10.1586/1744666X.1.1.87.

Abstract

Progenitor cells play important roles in the physiology and homeostasis of the overall hemopoietic system. The majority of hemopoietic activity takes place in the bone marrow, under the influence of resident marrow stromal cells, accessory cells, and/or their products. This constitutes the complex network of the hemopoietic inductive microenvironment, which is crucial for providing signals necessary for the maintenance of populations of progenitors at varying stages of lineage commitment. Accumulation of eosinophils and basophils in tissues is characteristic of allergic inflammation. A large body of evidence now exists which confirms that these tissue inflammatory events are coincident with relevant changes in progenitors; it has thus been hypothesized that the observed changes in mature cell numbers occur directly or indirectly as a result of differentiation of lineage-committed eosinophil/basophil, and perhaps other, progenitor cells. Differentiation and maturation of hemopoietic cells have traditionally been thought to be restricted to the bone marrow microenvironment. More recently, evidence has accumulated to suggest that some hemopoietic cells present in allergic tissue may be recruited from the bone marrow, traffic through the peripheral circulation and into tissues to participate in the ongoing inflammatory process at these distal sites. The clinical administration of monotherapy with topical corticosteroids, oral cysteinyl leukotriene antagonists and cytokine antagonists such as antibodies to interleukin-5, suggest that suppression of hemopoietic contributions to allergic inflammation may be necessary for full control of allergic inflammation and disease manifestations. In addition to progenitors being targets of therapy, they may well determine how and whether allergic inflammation is generated in early life, thus serving as biomarkers of disease.

摘要

祖细胞在整个造血系统的生理和稳态中发挥重要作用。大多数造血活动发生在骨髓中,受驻留骨髓基质细胞、辅助细胞和/或其产物的影响。这构成了造血诱导微环境的复杂网络,对于提供维持处于不同谱系承诺阶段的祖细胞所需的信号至关重要。组织中嗜酸性粒细胞和嗜碱性粒细胞的积累是过敏炎症的特征。大量证据证实,这些组织炎症事件与祖细胞的相关变化同时发生;因此,有人假设观察到的成熟细胞数量的变化直接或间接地是由于谱系承诺的嗜酸性粒细胞/嗜碱性粒细胞和其他祖细胞的分化所致。造血细胞的分化和成熟传统上被认为仅限于骨髓微环境。最近,有证据表明,过敏组织中存在的一些造血细胞可能来自骨髓,通过外周循环进入组织,参与这些远端部位的持续炎症过程。局部皮质类固醇、口服半胱氨酰白三烯拮抗剂和细胞因子拮抗剂(如白细胞介素-5 的抗体)的单一疗法的临床应用表明,抑制造血对过敏炎症的贡献可能是全面控制过敏炎症和疾病表现所必需的。除了祖细胞是治疗的靶点外,它们很可能决定过敏炎症是否以及如何在早期发生,从而成为疾病的生物标志物。

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