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轴器和咽是海胆造血的部位。

The Axial Organ and the Pharynx Are Sites of Hematopoiesis in the Sea Urchin.

机构信息

Department of Biological Sciences, George Washington University, Washington, DC, United States.

出版信息

Front Immunol. 2019 Apr 25;10:870. doi: 10.3389/fimmu.2019.00870. eCollection 2019.

Abstract

The location of coelomocyte proliferation in adult sea urchins is unknown and speculations since the early 1800s have been based on microanatomy and tracer uptake studies. In adult sea urchins () with down-regulated immune systems, coelomocyte numbers increase in response to immune challenge, and whether some or all of these cells are newly proliferated is not known. The gene regulatory network that encodes transcription factors that control hematopoiesis in embryonic and larval sea urchins has not been investigated in adults. Hence, to identify the hematopoietic tissue in adult sea urchins, cell proliferation, expression of phagocyte specific genes, and expression of genes encoding transcription factors that function in the conserved regulatory network that controls hematopoiesis in embryonic and larval sea urchins were investigated for several tissues. Cell proliferation was induced in adult sea urchins either by immune challenge through injection of heat-killed or by cell depletion through aspiration of coelomic fluid. In response to either of these stimuli, newly proliferated coelomocytes constitute only about 10% of the cells in the coelomic fluid. In tissues, newly proliferated cells and cells that express SpTransformer proteins (formerly Sp185/333) that are markers for phagocytes are present in the axial organ, gonad, pharynx, esophagus, and gut with no differences among tissues. The expression level of genes encoding transcription factors that regulate hematopoiesis show that both the axial organ and the pharynx have elevated expression compared to coelomocytes, esophagus, gut, and gonad. Similarly, an RNAseq dataset shows similar results for the axial organ and pharynx, but also suggests that the axial organ may be a site for removal and recycling of cells in the coelomic cavity. Results presented here are consistent with previous speculations that the axial organ may be a site of coelomocyte proliferation and that it may also be a center for cellular removal and recycling. A second site, the pharynx, may also have hematopoietic activity, a tissue that has been assumed to function only as part of the intestinal tract.

摘要

成年海胆中腔细胞增殖的位置尚不清楚,自 19 世纪初以来的推测一直基于微解剖学和示踪剂摄取研究。在免疫系统受到抑制的成年海胆中,腔细胞数量会在受到免疫挑战时增加,而这些细胞中是否有一些或全部是新增殖的尚不清楚。在成年海胆中,尚未研究编码控制胚胎和幼虫期海胆造血的转录因子的基因调控网络。因此,为了确定成年海胆中的造血组织,研究了几种组织中的细胞增殖、吞噬细胞特异性基因的表达以及编码在胚胎和幼虫期海胆中控制造血的保守调控网络中起作用的转录因子的基因表达。在成年海胆中,通过注射热灭活的细菌或通过抽吸体腔液来诱导细胞耗竭,从而诱导细胞增殖。对这两种刺激物的任何一种反应,新增殖的腔细胞仅构成体腔液中细胞的约 10%。在组织中,新增殖的细胞和表达 SpTransformer 蛋白(以前称为 Sp185/333)的细胞(吞噬细胞的标志物)存在于轴器官、性腺、咽、食管和肠道中,组织之间没有差异。调节造血的转录因子的基因表达水平表明,与腔细胞、食管、肠道和性腺相比,轴器官和咽都具有更高的表达水平。同样,一个 RNAseq 数据集表明轴器官和咽具有相似的结果,但也表明轴器官可能是腔室中细胞去除和再循环的部位。这里呈现的结果与以前的推测一致,即轴器官可能是腔细胞增殖的部位,它也可能是细胞去除和再循环的中心。第二个部位,咽,也可能具有造血活性,而该组织以前被认为仅作为肠道的一部分发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdb4/6494969/994a038d5928/fimmu-10-00870-g0001.jpg

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