Sogabe Shunsuke, Nakanishi Nagayasu, Degnan Bernard M
School of Biological Sciences, University of Queensland, Brisbane, QLD 4072 Australia.
Evodevo. 2016 Mar 8;7:6. doi: 10.1186/s13227-016-0042-x. eCollection 2016.
The aquiferous body plan of poriferans revolves around internal chambers comprised of choanocytes, a cell type structurally similar to choanoflagellates. These choanocyte chambers perform a range of physiological and developmental functions, including the capture of food and the generation of stem cells. Despite the increasing interest for choanocytes as sponge stem cells, there is limited knowledge on the development of choanocyte chambers. Using a combination of cell lineage tracing, antibody staining and EdU labeling, here we examine the development of choanocytes and the chambers they comprise during metamorphosis in the marine demosponge Amphimedon queenslandica.
Lineage-tracing experiments show that larval epithelial cells transform into mesenchymal pluripotent stem cells, resembling archeocytes, within 24 h of initiating metamorphosis. By 36 h, some of these labeled archeocyte-like cells have differentiated into choanocytes that will form the first postlarval choanocyte chambers. Non-labeled cells also contribute to these primary choanocyte chambers, consistent with these chambers being a chimera of multiple transdifferentiated larval cell types and not the proliferation of a single choanocyte precursor. Moreover, cell proliferation assays demonstrate that, following the initial formation of choanocyte chambers, chambers grow at least partially by the proliferation of choanocytes within the chamber, although recruitment of individual cells into established chambers also appears to occur. EdU labeling of postlarvae and juveniles reveals that choanocyte chambers are the primary location of cell proliferation during metamorphosis.
Our results show that multiple larval cell lineages typically contribute to formation of individual choanocyte chambers at metamorphosis, contrary to previous reports in other species that show sponge choanocyte chambers form clonally. Choanocytes in postlarval and juvenile A. queenslandica chambers can also divide, with choanocyte chambers being the primary location of cell proliferation. Interestingly, the level of cell proliferation varies greatly between chambers and appears to be contingent on the size, location and developmental state of the chamber. Small chambers on the periphery of the body tend to possess more dividing cells. As choanocytes can also dedifferentiate into archeocyte-like cells, cell proliferation in chambers may not only contribute to chamber growth and self-renewal but also increase the number of pluripotent archeocytes.
多孔动物的含水身体结构围绕着由领细胞组成的内部腔室展开,领细胞是一种在结构上与领鞭毛虫相似的细胞类型。这些领细胞腔室执行一系列生理和发育功能,包括捕获食物和产生干细胞。尽管人们对领细胞作为海绵干细胞的兴趣日益增加,但关于领细胞腔室发育的知识却很有限。我们结合细胞谱系追踪、抗体染色和EdU标记,研究了海洋寻常海绵纲的昆士兰双盘海绵在变态过程中领细胞及其组成的腔室的发育情况。
谱系追踪实验表明,幼虫上皮细胞在变态开始后的24小时内转变为间充质多能干细胞,类似于原始细胞。到36小时时,一些这些标记的类原始细胞已分化为领细胞,这些领细胞将形成幼虫后的首个领细胞腔室。未标记的细胞也对这些初级领细胞腔室有贡献,这与这些腔室是多种转分化幼虫细胞类型的嵌合体而非单个领细胞前体的增殖一致。此外,细胞增殖分析表明,在领细胞腔室最初形成后,腔室至少部分地通过腔室内领细胞的增殖而生长,尽管单个细胞也似乎会被招募到已有的腔室中。对幼虫后和幼年个体的EdU标记显示,领细胞腔室是变态过程中细胞增殖的主要部位。
我们的结果表明,在变态过程中,多个幼虫细胞谱系通常会参与单个领细胞腔室的形成,这与之前在其他物种中的报道相反,之前的报道显示海绵领细胞腔室是克隆形成的。幼虫后和幼年昆士兰双盘海绵腔室中的领细胞也可以分裂,领细胞腔室是细胞增殖的主要部位。有趣的是,不同腔室之间的细胞增殖水平差异很大,这似乎取决于腔室的大小、位置和发育状态。身体外围的小腔室往往有更多正在分裂的细胞。由于领细胞也可以去分化为类原始细胞,腔室内的细胞增殖不仅可能有助于腔室生长和自我更新,还可能增加多能原始细胞的数量。