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HIV Reprograms Human Airway Basal Stem/Progenitor Cells to Acquire a Tissue-Destructive Phenotype

机译:HIV重编程人气道基础干细胞/祖细胞以获取组织破坏性表型

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While highly active anti-retroviral therapy has dramatically improved the survival of HIV-infected individuals, there is an increased risk for other co-morbidities, such as COPD, manifesting as emphysema. Given that emphysema originates around the airways and that human airway basal cells (BCs) are adult airway stem/progenitor cells, we hypothesized that HIV reprograms BCs to a distinct phenotype that contributes to the development of emphysema. Our data indicate that HIV binds to but does not replicate in BCs. HIV binding to BCs induces them to acquire an invasive phenotype, mediated by upregulation of MMP-9 expression through activation of MAPK signaling pathways. This HIV-induced ''destructive'' phenotype may contribute to degradation of extracellular matrix and tissue damage relevant to the development of emphysema commonly seen in HIV^+ individuals.
机译:尽管高效的抗逆转录病毒疗法极大地提高了感染HIV的个体的生存率,但其他合并症(如CO​​PD)表现为肺气肿的风险却增加了。鉴于肺气肿起源于气道,而人气道基底细胞(BCs)是成年气道干/祖细胞,我们假设HIV将BCs重编程为有助于肺气肿发展的独特表型。我们的数据表明,HIV与BC结合但不能复制。 HIV与BCs的结合会诱导它们获得侵袭性表型,其通过激活MAPK信号传导途径上调MMP-9表达来介导。这种HIV诱导的“破坏性”表型可能会导致细胞外基质的降解以及与在HIV +个体中常见的肺气肿发展有关的组织损伤。

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