Van Neste Dominique, Tobin Desmond J
Skinterface, 9, rue du Sondart, B-7500 Tournai, Belgium.
Micron. 2004;35(3):193-200. doi: 10.1016/j.micron.2003.11.006.
The tight coupling of hair follicle melanogenesis to the hair growth cycle dramatically distinguishes follicular melanogenesis from the continuous melanogenesis of the epidermis. Cyclic re-construction of an intact hair follicle pigmentary unit occurs optimally in all scalp hair follicles during only the first 10 hair cycles, i.e. by approximately 40 years of age. Thereafter there appears to be a genetically regulated exhaustion of the pigmentary potential of each individual hair follicle leading to the formation of true gray and white hair. Pigment dilution results primarily from a reduction in tyrosinase activity within hair bulbar melanocytes. Thereafter, sub-optimal melanocyte-cortical keratinocyte interactions, and defective migration of melanocytes from a reservoir in the upper outer root sheath to the pigment-permitting microenvironment close to the follicular papilla of the hair bulb, will all disrupt normal function of the pigmentary unit. Evidence from studies on epidermal melanocyte aging suggest that reactive oxygen species-mediated damage to nuclear and mitochondrial DNA may lead to mutation accumulation in bulbar melanocytes. Parallel dysregulation of anti-oxidant mechanisms or pro/anti-apoptotic factors is also likely to occur within the cells. Pigment loss in canities may also affect keratinocyte proliferation and differentiation, providing the tantalizing suggestion that melanocytes in the hair follicle contribute far more that packages of pigment alone. Here, we review the current state of knowledge of the development, regulation and control of the aging human hair follicle pigmentary system in relation with hair cycling. The exploitation of recently available methodologies to manipulate hair follicle melanocytes in vitro, and the observations that melanocytes remain in senile white hair follicles that can be induced to pigment in culture, raises the possibility of someday reversing canities. The perspective of rejuvenation of the whole hair follicle apparatus are still part of the dream but optimising its functional properties is clinically relevant and is close to reality. Finally as hair color influences its visibility when optical methods such as scalp photography are used to count hair fibers, the attention is drawn to possible interpretations of statistically significant changes in visible hair. Such changes may not exclusively be related to improved hair growth itself but also to changes in natural hair color that makes the hair more visible with the method used to count hairs.
毛囊黑素生成与毛发生长周期的紧密耦合,使毛囊黑素生成与表皮的持续黑素生成显著区分开来。完整的毛囊色素单元的周期性重建仅在头10个毛发周期内,即在大约40岁之前,在所有头皮毛囊中最佳发生。此后,似乎存在一种由基因调控的每个毛囊色素生成潜能的耗尽,导致真正的灰发和白发形成。色素稀释主要是由于毛球黑素细胞中酪氨酸酶活性降低。此后,黑素细胞与皮质角质形成细胞之间的相互作用不理想,以及黑素细胞从外根鞘上部的储存库向靠近毛球毛囊乳头的色素允许微环境的迁移缺陷,都会破坏色素单元的正常功能。关于表皮黑素细胞衰老的研究证据表明,活性氧介导的对核DNA和线粒体DNA的损伤可能导致毛球黑素细胞中突变积累。细胞内抗氧化机制或促凋亡/抗凋亡因子的平行失调也可能发生。白发中的色素损失也可能影响角质形成细胞的增殖和分化,这提示毛囊中的黑素细胞的作用远不止提供色素包。在这里,我们综述了与毛发生长周期相关的衰老人类毛囊色素系统的发育、调节和控制的当前知识状态。利用最近可用的方法在体外操纵毛囊黑素细胞,以及观察到黑素细胞仍存在于老年白发毛囊中且在培养中可被诱导产生色素,这增加了有朝一日逆转白发的可能性。使整个毛囊装置恢复活力的前景仍然只是梦想的一部分,但优化其功能特性具有临床相关性且已接近现实。最后,由于在使用头皮摄影等光学方法计数毛发纤维时,头发颜色会影响其可见性,因此人们关注对可见头发中具有统计学意义变化的可能解释。这种变化可能不仅与头发生长本身的改善有关,还与自然头发颜色的变化有关,而这种变化使得用计数头发的方法更容易看到头发。