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干细胞异质性驱动 的寄生生活史。

Stem cell heterogeneity drives the parasitic life cycle of .

机构信息

Department of Bioengineering, Stanford University, Stanford, United States.

Department of Developmental Biology, Stanford University School of Medicine, Stanford, United States.

出版信息

Elife. 2018 Jul 10;7:e35449. doi: 10.7554/eLife.35449.

Abstract

Schistosomes are parasitic flatworms infecting hundreds of millions of people. These parasites alternate between asexual reproduction in molluscan hosts and sexual reproduction in mammalian hosts; short-lived, water-borne stages infect each host. Thriving in such disparate environments requires remarkable developmental plasticity, manifested by five body plans deployed throughout the parasite's life cycle. Stem cells in provide a potential source for such plasticity; however, the relationship between stem cells from different life-cycle stages remains unclear, as does the origin of the germline, required for sexual reproduction. Here, we show that subsets of larvally derived stem cells are likely sources of adult stem cells and the germline. We also identify a novel gene that serves as the earliest marker for the schistosome germline, which emerges inside the mammalian host and is ultimately responsible for disease pathology. This work reveals the stem cell heterogeneity driving the propagation of the schistosome life cycle.

摘要

血吸虫是寄生的扁形动物,感染了数亿人。这些寄生虫在软体动物宿主中进行无性繁殖,在哺乳动物宿主中进行有性繁殖;短暂的、水生的阶段感染每个宿主。在如此不同的环境中茁壮成长需要非凡的发育可塑性,表现在寄生虫生命周期中部署的五个身体计划中。提供了这种可塑性的潜在来源;然而,不同生命周期阶段的干细胞之间的关系以及生殖细胞的起源仍然不清楚,生殖细胞是有性繁殖所必需的。在这里,我们表明幼虫衍生的干细胞亚群可能是成虫干细胞和生殖细胞的来源。我们还鉴定了一个新基因,它作为血吸虫生殖细胞的最早标记物,该基因出现在哺乳动物宿主内,最终负责疾病病理学。这项工作揭示了驱动血吸虫生命周期传播的干细胞异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f50/6039179/cb2f0e2ad379/elife-35449-fig1.jpg

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