化学
硫酸乙酰肝素
乙酰肝素酶
低聚糖
细胞因子
MAPK/ERK通路
生物化学
人体皮肤
蛋白激酶B
癌症研究
生物活性
细胞
炎症
成纤维细胞
硫酸化
糖胺聚糖
黑色素瘤
内糖苷酶
哈卡特
角质形成细胞
药理学
组织蛋白酶D
作者
Clément Daviaud,Hugo Main,Damien Chassaing,Rachel Havret,Benjamin Musnier,Beatrice Colin,Jennifer Saliba,Manon Porta Zapata,Chanez Manseur,Rachida Mersni-Achour,Julien Cherfan,Jean‐François Jégou,Laure Favot-Laforge,H. Groult,Valérie Thiéry,Laurent Picot,Hugo Groult,Franck Morel,Kévin Baranger
标识
DOI:10.1016/j.biopha.2025.118954
摘要
Oligosaccharides that mimic heparan sulfate (HS) exhibit a variety of biological activities. One such oligosaccharide, λ-CO, a λ-carrageenan-derivative previously shown to inhibit cell migration, invasion, and heparanase 1 (HPA1), was evaluated for its anti-inflammatory properties. In LPS-stimulated macrophages, λ-CO significantly reduced Il-6 and Tnf-α production, as well as Erk and Akt phosphorylation, and Mmp-2/Mmp-9 secretion, independently of Hpa1 activity. In primary human keratinocytes stimulated with the psoriasis-mimicking M5 cytokine cocktail, λ-CO down-regulated cathepsin L and MMP-9 expression, as well as several M5-induced inflammatory genes. In vivo, λ-CO (1 and 10 mg.kg⁻¹) was administered in the imiquimod-induced mouse model of psoriasiform inflammation. Although no overt macroscopic improvement in skin lesions was evident, λ-CO at 10 mg.kg⁻¹ downregulated several inflammation-related genes in the skin and significantly reduced serum Mmp-9 levels. Taken together, these results suggest that λ-CO is a potential anti-inflammatory agent that selectively inhibits MMP-9 expression. This supports its further development as an adjunct to biotherapies for inflammatory skin disorders such as psoriasis.
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