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皮肤干燥、保湿和角质层松解。

Dry skin, moisturization and corneodesmolysis.

机构信息

Dept of Cell Biology and Physiology, Unilever Research, Colworth Laboratory, Sharnbrook, Bedford MK44 1LQ, U.K.

出版信息

Int J Cosmet Sci. 2000 Feb;22(1):21-52. doi: 10.1046/j.1467-2494.2000.00001.x.

Abstract

The process leading to the loss of corneocytes form the skin surface is termed desquamation. In healthy skin it is an orderly and essentially invisible process whereby individual or small groups of corneocytes detach from neighbouring cells to be lost to the environment and replaced by younger cells from the deeper layers. Desquamation is carefully controlled to ensure that corneum cohesion and integrity, and hence tissue thickness, is maintained. The most important components of the corneocytes contributing towards intercellular cohesion are the corneodesmosomes and lipids. Corneodesmosomes are proteinaceous complexes which effectively rivet corneocytes together. The intercellular lipids, primarily responsible for the water barrier, also provide part of the extracellular cement. In addition, the shape of the corneocyte itself plays a role in stratum corneum cohesion. Through interdigitation along their peripheral edges, adjacent corneocytes become physically locked together, a process which reinforces the integrity of the tissue. For effective desquamation to occur corneodesmosomes must be degraded: a process catalysed by serine proteases present within the intercellular space and facilitated by subtle changes in lipid composition and phase behaviour. Ultimately, it is the availability of free water which controls corneodesmolysis. In healthy skin this proteolytic process leaves relatively few corneodesmosomes intact in the most superficial layers. By contrast, in chronic and acute dry skin conditions, corneodesmosomal degradation and hence the final stages of desquamation are perturbed, leading to the characteristic formation of visible, powdery flakes on the skin surface. The inability to degrade these structures ultimately reflects a decreased hydrolytic activity of the desquamatory enzymes, either through reduced synthesis of the enzymes, inherent loss of activity, leaching from the surface layers of the corneum or changes in the surrounding lipid-rich microenvironment, which may indirectly reduce enzyme functionality. Increased understanding of the desquamation process is providing new insights into the mode of action of current moisturizing ingredients and is offering opportunities to develop novel therapies for preventing and correcting dry skin.

摘要

从皮肤表面脱落的角质形成细胞的过程称为脱屑。在健康的皮肤中,这是一个有序且基本不可见的过程,即单个或小群角质形成细胞从相邻细胞上脱离,然后丢失到环境中,并被来自深层的年轻细胞所取代。脱屑受到严格控制,以确保角质层的凝聚力和完整性,从而维持组织厚度。对细胞间凝聚力贡献最大的角质形成细胞成分是角质小体和脂质。角质小体是将角质形成细胞有效固定在一起的蛋白复合物。细胞间脂质主要负责水屏障,也提供部分细胞外胶。此外,角质形成细胞本身的形状也在角质层凝聚力中起作用。通过沿其边缘的相互交错,相邻的角质形成细胞在物理上相互锁定,这一过程增强了组织的完整性。为了实现有效的脱屑,必须降解角质小体:这一过程由细胞间隙中的丝氨酸蛋白酶催化,并通过脂质组成和相态变化的微妙变化来促进。最终,游离水的可用性控制着角质小体的溶解。在健康的皮肤中,这个蛋白水解过程使相对较少的角质小体在最浅层保持完整。相比之下,在慢性和急性干燥皮肤条件下,角质小体的降解和最终的脱屑阶段受到干扰,导致皮肤表面可见的、粉状薄片的特征性形成。这些结构无法降解最终反映了脱屑酶的水解活性降低,这可能是由于酶的合成减少、固有活性丧失、从角质层表面层浸出或周围富含脂质的微环境发生变化,这些变化可能间接降低酶的功能。对脱屑过程的深入了解为当前保湿成分的作用模式提供了新的见解,并为预防和纠正干燥皮肤提供了开发新型疗法的机会。

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