取自金银花(Lonicera japonica Thunb)的一种同型半乳糖酸。通过表皮生长因子受体和δ样4相关信号干扰血管生成。

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wenfeng Liao, Xiaodong Hu, Zhenyun Du, Peipei Wang, Kan Ding
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引用次数: 2

摘要

从金银花中提取纯化了一种均相多糖LJW2F2。结构特征表明LJW2F2为α-1,4- d -半乳糖醛酸组成的均半乳糖醛酸,分子量为7.2 kDa。以往的研究表明,均半乳糖酸可能阻碍血管生成,但其机制尚不清楚。本研究报道LJW2F2显著破坏基质上人微血管内皮细胞(HMEC-1)的毛细血管样管形成和细胞迁移。机制研究表明,LJW2F2可能使表皮生长因子受体(EGFR)磷酸化失活,进而抑制Raf、丝裂原活化蛋白激酶(MEK)和细胞外相关激酶(ERK)磷酸化。LJW2F2显著降低Notch1和δ样配体4 (Dll4)的表达。因此,我们的研究结果表明LJW2F2可能是一种潜在的血管生成抑制剂,通过干扰多种信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A homogalacturonan from Lonicera japonica Thunb. disrupts angiogenesis via epidermal growth factor receptor and Delta-like 4 associated signaling.

A homogalacturonan from Lonicera japonica Thunb. disrupts angiogenesis via epidermal growth factor receptor and Delta-like 4 associated signaling.

A homogeneous polysaccharide named as LJW2F2 was extracted and purified from the flowers of Lonicera japonica Thunb. Structural characteristic indicated that LJW2F2 was a homogalacturonan composed of α-1,4-D-galacturonic acid with a molecular weight of 7.2 kDa. Previous investigation suggested that homogalacturonan might impede angiogenesis, however the mechanism is still vague. Here we reported that LJW2F2 significantly disrupted capillary-like tube formation of human microvascular endothelia cells (HMEC-1) on matrigel as well as the cells migration. Mechanism study revealed that LJW2F2 might inactivate phosphorylation of epidermal growth factor receptor (EGFR), subsequently suppress Raf, mitogen-activated protein kinase (MEK) and extracellular-related kinase (ERK) phosphorylation. Moreover, LJW2F2 markedly decreased the expression of Notch1 and Delta-like ligand 4 (Dll4). Therefore, our results suggested that LJW2F2 might be a potential angiogenesis inhibitor via disturbing multiple signaling pathways.

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来源期刊
Glycoconjugate Journal
Glycoconjugate Journal 生物-生化与分子生物学
CiteScore
6.00
自引率
3.30%
发文量
63
审稿时长
1 months
期刊介绍: Glycoconjugate Journal publishes articles and reviews on all areas concerned with: function, composition, structure, biosynthesis, degradation, interactions, recognition and chemo-enzymatic synthesis of glycoconjugates (glycoproteins, glycolipids, oligosaccharides, polysaccharides and proteoglycans), biochemistry, molecular biology, biotechnology, immunology and cell biology of glycoconjugates, aspects related to disease processes (immunological, inflammatory, arthritic infections, metabolic disorders, malignancy, neurological disorders), structural and functional glycomics, glycoimmunology, glycovaccines, organic synthesis of glycoconjugates and the development of methodologies if biologically relevant, glycosylation changes in disease if focused on either the discovery of a novel disease marker or the improved understanding of some basic pathological mechanism, articles on the effects of toxicological agents (alcohol, tobacco, narcotics, environmental agents) on glycosylation, and the use of glycotherapeutics. Glycoconjugate Journal is the official journal of the International Glycoconjugate Organization, which is responsible for organizing the biennial International Symposia on Glycoconjugates.
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