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溶酶体作为甲型肝炎病毒颗粒成熟和非裂解性释放的平台。

Lysosomes serve as a platform for hepatitis A virus particle maturation and nonlytic release.

作者信息

Seggewiß Nicole, Paulmann Dajana, Dotzauer Andreas

机构信息

Laboratory of Virus Research, University of Bremen, Leobener Straße/UFT, 28359, Bremen, Germany.

出版信息

Arch Virol. 2016 Jan;161(1):43-52. doi: 10.1007/s00705-015-2634-5. Epub 2015 Oct 14.

Abstract

Early studies on hepatitis A virus (HAV) in cell culture demonstrated the inclusion of several viral particles in an intracellular lipid-bilayer membrane. However, the origin of these virus-associated membranes and the mechanism for the non-lytic release of HAV into bile are still unknown. Analyzing the association of this virus with cell organelles, we found that newly synthesized HAV particles accumulate in lysosomal organelles and that lysosomal enzymes are involved in the maturation cleavage of the virion. Furthermore, by inhibiting the processes of fusion of lysosomes with the plasma membrane, we found that the nonlytic release of HAV from infected cells occurs via lysosome-related organelles.

摘要

早期在细胞培养中对甲型肝炎病毒(HAV)的研究表明,细胞内脂质双层膜中包含多个病毒颗粒。然而,这些病毒相关膜的起源以及HAV非裂解性释放到胆汁中的机制仍不清楚。通过分析这种病毒与细胞器的关联,我们发现新合成的HAV颗粒积聚在溶酶体细胞器中,并且溶酶体酶参与病毒粒子的成熟切割。此外,通过抑制溶酶体与质膜的融合过程,我们发现受感染细胞中HAV的非裂解性释放是通过溶酶体相关细胞器发生的。

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