Department of Medical and Morphological Research, Udine, Italy.
Biol Rev Camb Philos Soc. 2010 May;85(2):347-60. doi: 10.1111/j.1469-185X.2009.00105.x. Epub 2009 Nov 24.
This review article is an attempt to trace the evolution of mast cells (MCs). These immune cells have been identified in all vertebrate classes as single-lobed cells containing variable amounts of membrane-bound secretory granules which store a large series of mediators, namely histamine, proteases, cytokines and growth factors. Other MC features, at least in mammals, are the c-kit receptor for the stem cell factor and the high-affinity receptor, FcepsilonRI, for immunoglobulin E (IgE). The c-kit receptor also has been identified in fish MCs. The FcepsilonRI receptor seems to be a more recent acquisition in MC phylogenesis given that IgE originated in mammalian species. Tryptase and histamine have also been recognized in MCs of teleost fish. Thus, a cell population with the overall characteristics of higher vertebrate MCs is identifiable in the most evolutionarily advanced fish species. Two potential MC progenitors have been identified in ascidians (urochordates which appeared approximately 500 million years ago): the basophil/MC-like granular haemocyte and the test cell. Both contain histamine and heparin, and provide defensive functions. Some granular haemocytes in Arthropoda also closely approximate the ultrastructure of modern MCs. The origin of MCs is probably to be found in a leukocyte ancestor operating in the context of a primitive local innate immunity and involved in phagocytic and killing activity against pathogens. From this type of defensive cell, the MC phylogenetic progenitor evolved into a tissue regulatory and remodelling cell, which was incorporated into the networks of recombinase activating genes (RAG)-mediated adaptive immunity in the Cambrian era, some 550 million years ago. Early MCs probably appeared in the last common ancestor we shared with hagfish, lamprey and sharks about 450-500 million years ago.
本文试图追溯肥大细胞(MCs)的演变。这些免疫细胞已在所有脊椎动物中被鉴定为具有单个叶的细胞,其中含有数量可变的膜结合分泌颗粒,这些颗粒储存着大量介质,即组胺、蛋白酶、细胞因子和生长因子。其他 MC 特征,至少在哺乳动物中,是干细胞因子的 c-kit 受体和免疫球蛋白 E(IgE)的高亲和力受体 FcepsilonRI。c-kit 受体也在鱼类 MCs 中被鉴定出来。鉴于 IgE 起源于哺乳动物物种,FcepsilonRI 受体似乎是 MC 系统发育中较新的获得物。类胰蛋白酶和组胺也在硬骨鱼的 MCs 中被识别。因此,在进化上最先进的鱼类物种中,可以识别出具有高等脊椎动物 MC 总体特征的细胞群体。在尾索动物(大约在 5 亿年前出现的脊索动物)中已经鉴定出两种潜在的 MC 前体:嗜碱性/MC 样颗粒血细胞和测试细胞。两者都含有组胺和肝素,并提供防御功能。节肢动物中的一些颗粒血细胞也非常接近现代 MCs 的超微结构。MC 的起源可能是在一种白细胞祖先中发现的,该祖先是在原始的局部先天免疫背景下运作的,参与了针对病原体的吞噬和杀伤活性。从这种防御细胞类型中,MC 进化祖先进化成为一种组织调节和重塑细胞,该细胞在寒武纪时代的重组激活基因(RAG)介导的适应性免疫网络中被纳入,大约在 5.5 亿年前。早期的 MCs 可能出现在我们与七鳃鳗、盲鳗和鲨鱼共享的最后共同祖先中,大约在 4.5 亿到 5 亿年前。