[成纤维细胞亚群:皮肤生理和衰老的发育方法]。

Journal de la Societe de biologie Pub Date : 2008-01-01 Epub Date: 2008-05-08 DOI:10.1051/jbio:2008002
Daniel Asselineau, Hervé Pageon, Solène Mine
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引用次数: 1

摘要

皮肤是一个器官,其功能远远超出了身体内外的物理屏障。皮肤作为一个整体受到老化的影响,这主要涉及皮肤的真皮和深层成分,也是它的物质成分。真皮是一种富含物质元素而细胞含量较低的组织,人们普遍认为,发生在基质中的修饰是通过改变其生物力学特性而导致皮肤老化的主要原因。因此,通过考虑胶原蛋白等基质分子的变化来解决与皮肤老化有关的问题是很常见的。实际上,真皮层是一个复杂的物质和细胞组织,分为接近表皮的浅层真皮层和更厚且在组织学上不同的深层真皮层。几年前,我们进行了有关成纤维细胞的研究,成纤维细胞是负责真皮形成和维持的细胞,旨在分离、培养和表征来自浅层真皮(也称为乳头状真皮)和深层真皮(也称为网状真皮)的成纤维细胞。我们能够证明,这些成纤维细胞在塑料上的经典培养中表现出与不同分泌特性相关的非常不同的形态,我们已经证实并扩展了这些观察结果,揭示了不同的表型,通过将这些细胞纳入重建皮肤中,可以在体内重现三维结构,特别是在移植到裸鼠身上后。我们还提出了这两个真皮区域在真皮形成过程中是如何出现的问题,以及它们在衰老过程中的命运。解决这些问题的进展肯定会对更好地理解皮肤生理学和衰老非常有用,并有望为抗衰老研究提供新的策略。
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[Fibroblast subpopulations: a developmental approach of skin physiology and ageing].
Skin is an organ whose function is far beyond a physical barrier between the inside and the outside of the body. Skin as the whole organism is subjected to ageing which concerns skin mostly in its dermal and deepest component which is also its matricial component. The dermis is a tissue rich in matricial elements and poor in cellular content and it is generally admitted that modifications occurring in the matrix are those which mostly contribute to skin ageing, by altering its biomechanical properties. Therefore it is common to address questions related to skin ageing by considering alterations in matrix molecules like collagen. Actually the dermis is a complex tissue both matricial and cellular and is divided between a superficial dermis close to epidermis and a deep dermis much thicker and histologically different. Several years ago we have undertaken investigations related to fibroblasts which are the cells responsible for the formation and maintenance of the dermis, aiming at isolation, culture and characterization of the fibroblasts from the superficial dermis also called papillary dermis and fibroblasts from the deep dermis also called reticular dermis. We were able to show that these fibroblasts in classical culture on plastic exhibit very different morphologies associated with different secretion properties and we have confirmed and expanded such observations revealing different phenotypes by incorporating these cells in reconstructed skin which allows the reproduction of a three-dimensional architecture recalling skin in vivo especially after grafting onto the nude mouse. We also raise the question of how these two dermal regions appear during the formation of the dermis and the question of their fate during ageing. Progress in solving these questions would certainly appear to be very useful for a better understanding of skin physiology and ageing and would hopefully provide new strategies in anti-ageing research.
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