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A Transient Developmental Hematopoietic Stem Cell Gives Rise to Innate-like B and T Cells

机译:瞬时发育的造血干细胞使先天性B和T细胞上升

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摘要

The generation of distinct hematopoietic cell types, including tissue-resident immune cells, distinguishes fetal from adult hematopoiesis. However, the mechanisms underlying differential cell production to generate a layered immune system during hematopoietic development are unclear. Using an irreversible lineage-tracing model, we identify a definitive hematopoietic stem cell (HSC) that supports long-term multilineage reconstitution upon transplantation into adult recipients but does not persist into adulthood in situ. These HSCs are fully multipotent, yet they display both higher lymphoid cell production and greater capacity to generate innate-like B and T lymphocytes as compared to coexisting fetal HSCs and adult HSCs. Thus, these developmentally restricted HSCs (drHSCs) define the origin and generation of early lymphoid cells that play essential roles in establishing self-recognition and tolerance, with important implications for understanding autoimmune disease, allergy, and rejection of transplanted organs.
机译:独特的造血细胞类型(包括组织驻留免疫细胞)的产生将胎儿与成人造血区分开来。但是,尚不清楚在造血过程中产生差异细胞以产生分层免疫系统的潜在机制。使用不可逆的谱系追踪模型,我们确定了确定的造血干细胞(HSC),该细胞支持在移植到成年受体中的长期多谱系重建,但不会原位持续到成年。这些HSC具有完全的多能性,但与胎儿HSC和成年HSC相比,它们既显示出更高的淋巴样细胞产量,又具有更高的生成先天性B和T淋巴细胞的能力。因此,这些受发育限制的HSC(drHSC)定义了早期淋巴样细胞的起源和产生,这些早期淋巴样细胞在建立自我识别和耐受性中起着至关重要的作用,对理解自身免疫性疾病,过敏和移植器官的排斥反应具有重要意义。

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