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巨噬细胞特异性基因表达:当前范式与未来挑战。

Macrophage-specific gene expression: current paradigms and future challenges.

作者信息

Greaves David R, Gordon Siamon

机构信息

Sir William Dunn School of Pathology, University of Oxford, United Kingdom.

出版信息

Int J Hematol. 2002 Jul;76(1):6-15. doi: 10.1007/BF02982713.

Abstract

Cells of the mononuclear phagocyte lineage include macrophages, microglia, osteoclasts, and myeloid dendritic cells. These cell types are all derived from blood monocytes, which are the product of hematopoietic stem cell differentiation. In this review we use specific examples of macrophage-expressed genes to illustrate potential regulatory strategies for directing macrophage-specific gene expression. The examples we have chosen-the human c-fes gene, the murine spi-1 (PU.1) gene, the human RANTES promoter, and the human CD68 gene-illustrate different aspects of constitutive and inducible gene expression in macrophages. One important challenge for future work in this field will be to identify the molecular events that dictate lineage decisions during the differentiation of mononuclear phagocytes from hematopoietic progenitor cells. Another important goal will be to understand how groups of macrophage genes are coordinately expressed in response to physiological, immunological, and inflammatory stimuli. A better understanding of macrophage gene expression may find application in gene therapy, genetic vaccination, and the development of new antiinflammatory drugs.

摘要

单核吞噬细胞谱系的细胞包括巨噬细胞、小胶质细胞、破骨细胞和髓样树突状细胞。这些细胞类型均源自血液单核细胞,而血液单核细胞是造血干细胞分化的产物。在本综述中,我们使用巨噬细胞表达基因的具体实例来说明指导巨噬细胞特异性基因表达的潜在调控策略。我们选择的实例——人类c-fes基因、小鼠spi-1(PU.1)基因、人类RANTES启动子和人类CD68基因——说明了巨噬细胞中组成型和诱导型基因表达的不同方面。该领域未来研究的一个重要挑战将是确定在造血祖细胞分化为单核吞噬细胞过程中决定细胞谱系分化的分子事件。另一个重要目标将是了解巨噬细胞基因群如何响应生理、免疫和炎症刺激而协调表达。对巨噬细胞基因表达的更好理解可能会应用于基因治疗、基因疫苗接种以及新型抗炎药物的开发。

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