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基质中的血管生成抑制信号:血管内皮细胞自噬与透明质酸生物学。

Angiostatic cues from the matrix: Endothelial cell autophagy meets hyaluronan biology.

机构信息

Translational Cellular Oncology Program, Sidney Kimmel Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Translational Cellular Oncology Program, Sidney Kimmel Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

出版信息

J Biol Chem. 2020 Dec 4;295(49):16797-16812. doi: 10.1074/jbc.REV120.014391. Epub 2020 Oct 5.

Abstract

The extracellular matrix encompasses a reservoir of bioactive macromolecules that modulates a cornucopia of biological functions. A prominent body of work posits matrix constituents as master regulators of autophagy and angiogenesis and provides molecular insight into how these two processes are coordinated. Here, we review current understanding of the molecular mechanisms underlying hyaluronan and HAS2 regulation and the role of soluble proteoglycan in affecting autophagy and angiogenesis. Specifically, we assess the role of proteoglycan-evoked autophagy in regulating angiogenesis via the HAS2-hyaluronan axis and ATG9A, a novel HAS2 binding partner. We discuss extracellular hyaluronan biology and the post-transcriptional and post-translational modifications that regulate its main synthesizer, HAS2. We highlight the emerging group of proteoglycans that utilize outside-in signaling to modulate autophagy and angiogenesis in cancer microenvironments and thoroughly review the most up-to-date understanding of endorepellin signaling in vascular endothelia, providing insight into the temporal complexities involved.

摘要

细胞外基质包含了大量具有生物活性的生物大分子,这些生物大分子可以调节丰富的生物学功能。大量研究表明,基质成分是自噬和血管生成的主要调节剂,并为这两个过程如何协调提供了分子见解。在这里,我们回顾了透明质酸和 HAS2 调节的分子机制以及可溶性蛋白聚糖在影响自噬和血管生成中的作用的最新认识。具体来说,我们评估了蛋白聚糖引发的自噬通过 HAS2-透明质酸轴和 ATG9A(一种新型 HAS2 结合伴侣)调节血管生成的作用。我们讨论了细胞外透明质酸生物学以及调节其主要合成酶 HAS2 的转录后和翻译后修饰。我们强调了一组新兴的蛋白聚糖,它们利用外向信号来调节癌症微环境中的自噬和血管生成,并彻底回顾了血管内皮细胞中内皮抑制素信号的最新认识,深入了解其中涉及的时间复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e38/7864073/4bec704b2a0f/gr1.jpg

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