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紫外线 B 照射激活硫酸乙酰肝素酶导致人皮肤表皮与真皮交界处基底膜功能丧失。

Activation of heparanase by ultraviolet B irradiation leads to functional loss of basement membrane at the dermal-epidermal junction in human skin.

机构信息

Shiseido Research Center, Hayabuchi, Tsuzuki-ku, Yokohama, Japan.

出版信息

Arch Dermatol Res. 2011 May;303(4):253-61. doi: 10.1007/s00403-010-1117-5. Epub 2011 Jan 11.

Abstract

Recently, we reported that heparanase plays important roles in barrier-disrupted skin, leading to increased interaction of growth factors between epidermis and dermis and facilitating various cutaneous changes, including epidermal hyperplasia and wrinkle formation. However, the role of heparanase in sun-exposed skin remains unknown. Here, we show that heparanase in human keratinocytes is activated by ultraviolet B (UVB) exposure and that heparan sulfate of perlecan is markedly degraded in UVB-irradiated human skin. The degradation of heparan sulfate resulted in a marked reduction of binding activity of the basement membrane for vascular endothelial growth factor, fibroblast growth factor-2 and -7 at the dermal-epidermal junction. Degradation of heparan sulfate was observed not only in acutely UVB-irradiated skin, but also in skin chronically exposed to sun. Interestingly, heparan sulfate was found to be degraded in sun-exposed skin, but not in sun-protected skin. These findings suggest that chronic UVB exposure activates heparanase, leading to degradation of heparan sulfate in the basement membrane and increased growth factor interaction between epidermis and dermis. These changes may facilitate photo-aging.

摘要

最近,我们报道了肝素酶在屏障破坏的皮肤中发挥重要作用,导致表皮和真皮之间生长因子的相互作用增加,促进各种皮肤变化,包括表皮增生和皱纹形成。然而,肝素酶在暴露于阳光的皮肤中的作用尚不清楚。在这里,我们表明人角质形成细胞中的肝素酶被紫外线 B(UVB)暴露激活,并且在 UVB 照射的人皮肤中明显降解了多配体聚糖的硫酸乙酰肝素。硫酸乙酰肝素的降解导致基底膜与血管内皮生长因子、成纤维细胞生长因子-2 和 -7 的结合活性显著降低,位于表皮与真皮交界处。不仅在急性 UVB 照射的皮肤中观察到硫酸乙酰肝素的降解,而且在长期暴露于阳光的皮肤中也观察到硫酸乙酰肝素的降解。有趣的是,在暴露于阳光的皮肤中发现硫酸乙酰肝素降解,而在防晒皮肤中未发现。这些发现表明慢性 UVB 暴露激活肝素酶,导致基底膜中硫酸乙酰肝素降解,并增加表皮和真皮之间生长因子的相互作用。这些变化可能促进光老化。

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