首页> 外文期刊>American Journal of Physical Anthropology >Basis for the gain and subsequent dilution of epidermal pigmentation during human evolution: The barrier and metabolic conservation hypotheses revisited
【24h】

Basis for the gain and subsequent dilution of epidermal pigmentation during human evolution: The barrier and metabolic conservation hypotheses revisited

机译:人类进化过程中表皮色素沉着的获得和随后稀释的基础:重新审视了屏障和代谢保守性假设

获取原文
获取原文并翻译 | 示例
       

摘要

The evolution of human skin pigmentation must address both the initial evolution of intense epidermal pigmentation in hominins, and its subsequent dilution in modern humans. While many authorities believe that epidermal pigmentation evolved to protect against either ultraviolet B (UV-B) irradiation-induced mutagenesis or folic acid photolysis, we hypothesize that pigmentation augmented the epidermal barriers by shifting the UV-B dose-response curve from toxic to beneficial. Whereas erythemogenic UV-B doses produce apoptosis and cell death, suberythemogenic doses benefit permeability and antimicrobial function. Heavily melanized melanocytes acidify the outer epidermis and emit paracrine signals that augment barrier competence. Modern humans, residing in the cooler, wetter climes of south-central Europe and Asia, initially retained substantial pigmentation. While their outdoor lifestyles still permitted sufficient cutaneous vitamin D3 (VD3) synthesis, their marginal nutritional status, coupled with cold-induced caloric needs, selected for moderate pigment reductions that diverted limited nutritional resources towards more urgent priorities (5metabolic conservation). The further pigment-dilution that evolved as humans reached north-central Europe (i.e., northern France, Germany), likely facilitated cutaneous VD3 synthesis, while also supporting ongoing, nutritional requirements. But at still higher European latitudes where little UV-B breaches the atmosphere (i.e., present-day UK, Scandinavia, Baltic States), pigment dilution alone could not suffice. There, other nonpigment-related mutations evolved to facilitate VD3 production; for example, in the epidermal protein, filaggrin, resulting in reduced levels of its distal metabolite, trans-urocanic acid, a potent UV-B chromophore. Thus, changes in human pigmentation reflect a complex interplay between latitude, climate, diet, lifestyle, and shifting metabolic priorities.
机译:人类皮肤色素沉着的演变必须解决人参素中强烈的表皮色素沉着的最初演变以及其在现代人类中的稀释作用。尽管许多权威人士认为表皮色素沉着逐渐发展为可以防止紫外线B(UV-B)辐射诱变或叶酸光解,但我们假设色素沉着通过将UV-B剂量反应曲线从有毒变为有益而增加了表皮屏障。 。产生红斑的UV-B剂量可导致细胞凋亡和细胞死亡,而产生红斑的UV-B剂量可改善通透性和抗菌功能。严重黑色素化的黑素细胞会酸化外表皮并发出旁分泌信号,从而增强屏障功能。居住在欧洲中南部和亚洲较凉爽,潮湿的气候中的现代人类最初保留了大量色素。尽管他们的户外生活方式仍然可以使皮肤维生素D3(VD3)充分合成,但他们的边缘营养状况以及寒冷引起的热量需求被选择为中等程度的色素减少,这将有限的营养资源转移到了更紧迫的优先事项上(5代谢保存)。随着人类到达欧洲中北部(即法国北部,德国)而进一步发展的色素稀释作用,可能促进了皮肤VD3的合成,同时也满足了持续的营养需求。但是在更高的欧洲纬度,几乎没有UV-B破坏大气层(即当今的英国,斯堪的纳维亚半岛,波罗的海国家),仅靠颜料稀释是不够的。在那里,其他非色素相关的突变进化出以促进VD3的产生。例如,在表皮蛋白丝聚蛋白中,其远端代谢产物反式尿烷酸(一种有效的UV-B发色团)水平降低。因此,人类色素沉着的变化反映了纬度,气候,饮食,生活方式和不断变化的代谢优先顺序之间的复杂相互作用。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号