Cooper E L, Kvell K, Engelmann P, Nemeth P
Laboratory of Comparative Neuroimmunology, Department of Neurobiology, David Geffen School of Medicine at UCLA, University of California, Los Angeles, LA 90095-1763, USA.
Immunol Lett. 2006 Apr 15;104(1-2):18-28. doi: 10.1016/j.imlet.2005.11.012. Epub 2005 Dec 5.
Multicellular organisms including invertebrates and vertebrates live in various habitats that may be aquatic or terrestrial where they are constantly exposed to deleterious pathogens. These include viruses, bacteria, fungi, and parasites. They have evolved various immunodefense mechanisms that may protect them from infection by these microorganisms. These include cellular and humoral responses and the level of differentiation of the response parallels the evolutionary development of the species. The first line of innate immunity in earthworms is the body wall that prevents the entrance of microbes into the coelomic cavity that contains fluid in which there are numerous leukocyte effectors of immune responses. When this first barrier is broken, a series of host responses is set into motion activating the leukocytes and the coelomic fluid. The responses are classified as innate, natural, non-specific, non-anticipatory, non-clonal (germ line) in contrast to the vertebrate capacity that is considered adaptive, induced, specific, anticipatory and clonal (somatic). Specific memory is associated with the vertebrate response and there is information that the innate response of invertebrates may under certain conditions possess specific memory. The invertebrate system when challenged affects phagocytosis, encapsulation, agglutination, opsonization, clotting and lysis. At least two major leukocytes, small and large mediate lytic reactions against several tumor cell targets. Destruction of tumor cells in vitro shows that phagocytosis and natural killer cell responses are distinct properties of these leukocytes. This has prompted newer searches for immune function and regulation in other systems. The innate immune system of the earthworm has been analyzed for more than 40 years with every aspect examined. However, there are no known entire sequences of the earthworm as exists in these other invertebrates. Because the earthworm lives in soil and has been utilized as a successful monitor for pollution, there are studies that reveal up and down regulation of responses in the immune system after exposure to a variety of environmental pollutants. Moreover, there are partial sequences that appear in earthworms after exposure to environmental pollutants such as cadmium and copper. There are now attempts to define the AHR receptor crucial for intracellular signaling after exposure to pollutants, but without linking the signals to changes in the immune system. There are several pathways for signal transduction, including JAK/STAT, TOLL, TRAF PIP3, known in invertebrates and vertebrates. For resistance to pathogens, conserved signal transduction components are required and these include a Toll/IL-1 receptor domain adaptor protein that functions upstream of a conserved p38 MAP kinase pathway. This pathway may be an ancestral innate immune signaling pathway found in a putative common ancestor of nematodes, arthropods and even vertebrates. It could also help us to link pollution, innate immunity and transduction in earthworms.
包括无脊椎动物和脊椎动物在内的多细胞生物生活在各种栖息地中,这些栖息地可能是水生或陆生的,它们在其中不断接触有害病原体。这些病原体包括病毒、细菌、真菌和寄生虫。它们进化出了各种免疫防御机制,以保护自己免受这些微生物的感染。这些机制包括细胞和体液反应,反应的分化程度与物种的进化发展并行。蚯蚓先天免疫的第一道防线是体壁,它可防止微生物进入体腔,体腔中含有液体,其中有许多免疫反应的白细胞效应器。当这第一道屏障被打破时,一系列宿主反应就会启动,激活白细胞和体腔液。与被认为是适应性、诱导性、特异性、预期性和克隆性(体细胞性)的脊椎动物能力相比,这些反应被归类为先天的、天然的、非特异性的、非预期性的、非克隆性(种系)的。特异性记忆与脊椎动物的反应相关,有信息表明无脊椎动物的先天反应在某些情况下可能具有特异性记忆。无脊椎动物系统受到挑战时会影响吞噬作用、包囊化、凝集、调理作用、凝血和裂解。至少有两种主要的白细胞,即小白细胞和大白细胞介导针对几种肿瘤细胞靶标的裂解反应。体外肿瘤细胞的破坏表明吞噬作用和自然杀伤细胞反应是这些白细胞的不同特性。这促使人们在其他系统中对免疫功能和调节进行更新的研究。蚯蚓的先天免疫系统已经被分析了40多年,各个方面都进行了研究。然而,与这些其他无脊椎动物不同,目前还没有已知的蚯蚓全序列。由于蚯蚓生活在土壤中,并且已被用作污染的成功监测指标,有研究表明,接触各种环境污染物后,蚯蚓免疫系统的反应会出现上调和下调。此外,接触镉和铜等环境污染物后,蚯蚓体内会出现部分序列。现在有人试图确定接触污染物后对细胞内信号传导至关重要的芳烃受体(AHR),但没有将这些信号与免疫系统的变化联系起来。信号转导有几种途径,包括无脊椎动物和脊椎动物中已知的JAK/STAT、TOLL、TRAF PIP3。为了抵抗病原体,需要保守的信号转导成分,其中包括一种Toll/IL-1受体结构域衔接蛋白,它在保守的p38丝裂原活化蛋白激酶(MAP)途径上游起作用。这条途径可能是在一种假定的线虫、节肢动物甚至脊椎动物的共同祖先中发现的祖传先天免疫信号传导途径。它也可以帮助我们将蚯蚓中的污染、先天免疫和转导联系起来。