Müller W E G, Wiens M, Müller I M, Schröder H C
Institut für Physiologische Chemie, Abteilung Angewandte Molekularbiologie, Universität, Duesbergweg 6, 55099 Mainz, Germany.
Prog Mol Subcell Biol. 2004;34:103-43. doi: 10.1007/978-3-642-18670-7_5.
Porifera (sponges) are now well accepted as the phylum which branched off first from the common ancestor of all metazoans, the Urmetazoa. The transition to the Metazoa became possible because during this phase, cell-cell as well as cell-matrix adhesion molecules evolved which allowed the formation of a colonial stage of animals. The next prerequisite for the evolution to the Urmetazoa was the establishment of an effective immune system which, flanked by apoptosis, allowed the formation of a first level of individuation. In sponges (with the model Suberites domuncula and Geodia cydonium), the main mediators of the immune responses are the chemokines. Since sponges lack a vascular system and consequently blood cells (in the narrow sense), we have used the term chemokines (in a broad sense) to highlight that the complex network of intercellular mediators initiates besides differentiation processes also cell movement. In the present review, the cDNAs encoding the following chemokines were described and the roles of their deduced proteins during self-self and nonself recognition outlined: the allograft inflammatory factor, the glutathione peroxidase, the endothelial-monocyte-activating polypeptide, the pre-B-cell colony-enhancing factor and the myotrophin as well as an enzyme, the (2-5)A synthetase, which is involved in cytokine response in vertebrates. A further step required to reach the evolutionary step of the integrated stage of the Urmetazoa was the acquisition of a stem cell system. In this review, first markers for stem cells (mesenchymal stem cell-like protein) as well as for chemokines involved in the maintenance of stem cells (noggin and glia maturation factor) are described at the molecular level, and a first functional analysis is approached. Taken together, it is outlined that the chemokine network was essential for the establishment of metazoans, which evolved approximately 600 to 800 million years ago.
多孔动物门(海绵)现在已被广泛认可为最早从所有后生动物的共同祖先——原始后生动物分支出来的门。向后生动物的转变成为可能,是因为在此阶段,细胞间以及细胞与基质的黏附分子得以进化,这使得动物能够形成群体阶段。向原始后生动物进化的下一个先决条件是建立有效的免疫系统,该系统在细胞凋亡的辅助下,允许形成第一层个体性。在海绵动物中(以多管海绵属和地穴海绵属为模型),免疫反应的主要介质是趋化因子。由于海绵缺乏血管系统,因而也缺乏狭义上的血细胞,我们使用“趋化因子”(广义)这一术语来强调细胞间介质的复杂网络除了启动分化过程外,还能引发细胞运动。在本综述中,描述了编码以下趋化因子的cDNA,并概述了其推导蛋白在自身与非自身识别过程中的作用:同种异体移植炎症因子、谷胱甘肽过氧化物酶、内皮单核细胞激活多肽、前B细胞集落增强因子和肌营养蛋白,以及一种参与脊椎动物细胞因子反应的酶——(2-5)A合成酶。达到原始后生动物整合阶段进化步骤所需的进一步发展是获得干细胞系统。在本综述中,在分子水平上描述了干细胞的首个标志物(间充质干细胞样蛋白)以及参与维持干细胞的趋化因子(头蛋白和神经胶质成熟因子),并进行了初步的功能分析。综上所述,趋化因子网络对于后生动物的建立至关重要,后生动物大约在6亿至8亿年前进化而来。