通过表面标记筛选和基因表达谱分析解密禽类造血干细胞

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-16 DOI:10.1016/j.molimm.2024.09.003
Neslihan Meriç , Pınar Çolakoğlu Erkan , Fatih Kocabaş
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引用次数: 0

摘要

背景禽类在发育造血研究中发挥了关键作用,带来了许多重要发现。禽流感,尤其是 H5N1 株,对家禽构成了重大威胁,并有可能传染给人类。感染通常会导致异常的血液学特征,突显了禽类疾病与造血之间复杂的相互作用。许多禽类疾病会抑制骨髓(BM)中的免疫细胞,影响免疫反应。研究禽类骨髓中的造血干细胞(HSCs)对于了解这些过程以及为禽类和人类健康开发有效的疫苗和保护策略至关重要。这些分离出的细胞被进一步鉴定为 Lin-Sca1+c-Kit+ (LSK),并发现它们比对照组更为普遍。RT-PCR分析显示,在这些干细胞中,MEIS1和TSC1等基因上调,而SIRT1、FOXO1和AHR等基因下调。对LSK标记的筛选显示,Sca1+c-Kit+细胞群中有十种独特的表面抗原,包括CD178、CD227和CD184等高度富集的抗原。此外,对鹌鹑造血干细胞的研究表明,类似的标记技术在鹌鹑BM中也很有效。研究结果表明,禽造血干细胞特异性表面抗原的鉴定为禽流感和其他疾病的发病机制提供了有价值的见解,加深了我们对这些疾病如何抑制造血干细胞功能的理解。值得注意的是,LSK 细胞中 MEIS1 和 TSC1 基因的上调强调了它们在调节造血过程中的关键作用。相反,SIRT1、FOXO1 和 AHR 基因的下调则为它们在分化和免疫反应机制中的作用提供了重要线索。讨论本研究的发现通过识别禽类造血干细胞特异性的表面标记物,加深了我们对禽类疾病对免疫系统影响的理解。流感等病原体对造血干细胞功能的抑制凸显了了解这些细胞对开发靶向疫苗的重要性。这些结果标志着通过降低与禽类病原体相关的风险来改善全球健康安全迈出了重要一步。
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Deciphering avian hematopoietic stem cells by surface marker screening and gene expression profiling

Background

Avian species have played a pivotal role in developmental hematopoiesis research, leading to numerous critical discoveries. Avian influenza, particularly the H5N1 strain, poses a significant threat to poultry and has zoonotic potential for humans. Infections often result in abnormal hematologic profiles, highlighting the complex interplay between avian diseases and hematopoiesis. Many avian diseases can suppress immune cells in the bone marrow (BM), impacting immune responses. Studying hematopoietic stem cells (HSCs) in avian BM is crucial for understanding these processes and developing effective vaccines and protection strategies for both avian and human health.

Methods

This study adapted methods from mouse studies to isolate avian HSCs as Lineage-negative (Lin-) cells. These isolated cells were further identified as Lin-Sca1+c-Kit+ (LSK) and were found to be more prevalent than in control groups. RT-PCR analyses were conducted, showing that genes like MEIS1 and TSC1 were upregulated, while SIRT1, FOXO1, and AHR were downregulated in these stem cells. Screening for LSK markers revealed ten unique surface antigens in the Sca1+c-Kit+ cell populations, including highly enriched antigens such as CD178, CD227, and CD184. Additionally, studies on quail HSCs demonstrated that similar labeling techniques were effective in quail BM.

Results

The research demonstrated that the identification of avian HSC-specific surface antigens provides valuable insights into the pathogenesis of avian influenza and other diseases, enhancing our understanding of how these diseases suppress HSC function. Notably, the upregulation of MEIS1 and TSC1 genes in LSK cells underscores their critical roles in regulating hematopoietic processes. Conversely, the downregulation of SIRT1, FOXO1, and AHR genes provides important clues about their roles in differentiation and immune response mechanisms.

Discussion

The findings of this study deepen our understanding of the effects of avian diseases on the immune system by identifying surface markers specific to avian HSCs. The suppression of HSC function by pathogens such as influenza highlights the importance of understanding these cells in developing targeted vaccines. These results represent a significant step towards improving global health security by mitigating risks associated with avian pathogens.

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CiteScore
7.20
自引率
4.30%
发文量
567
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