Laboratory of Molecular Developmental Biology, Department of Biophysics, Graduate School of Science, Kyoto-University, Kitashirakawa-Oiwake, Sakyo-ku, Kyoto 606-8502, Japan.
Evol Dev. 2010 May-Jun;12(3):275-87. doi: 10.1111/j.1525-142X.2010.00413.x.
Little is known about the stem cells of organisms early in metazoan evolution. To characterize the stem cell system in demosponges, we identified Piwi homologs of a freshwater sponge, Ephydatia fluviatilis, as candidate stem cell (archeocyte) markers. EfPiwiA mRNA was expressed in cells with archeocyte cell morphological features. We demonstrated that these EfPiwiA-expressing cells were indeed stem cells by showing their ability to proliferate, as indicated by BrdU-incorporation, and to differentiate, as indicated by the coexpression of EfPiwiA with cell-lineage-specific genes in presumptive committed archeocytes. EfPiwiA mRNA expression was maintained in mature choanocytes forming chambers, in contrast to the transition of gene expression from EfPiwiA to cell-lineage-specific markers during archeocyte differentiation into other cell types. Choanocytes are food-entrapping cells with morphological features similar to those of choanoflagellates (microvillus collar and a flagellum). Their known abilities to transform into archeocytes under specific circumstances and to give rise to gametes (mostly sperm) indicate that even when they are fully differentiated, choanocytes maintain pluripotent stem cell-like potential. Based on the specific expression of EfPiwiA in archeocytes and choanocytes, combined with previous studies, we propose that both archeocytes and choanocytes are components of the demosponge stem cell system. We discuss the possibility that choanocytes might represent the ancestral stem cells, whereas archeocytes might represent stem cells that further evolved in ancestral multicellular organisms.
关于后生动物早期的生物体干细胞,我们知之甚少。为了描述淡水海绵 Ephydatia fluviatilis 的干细胞系统,我们鉴定了 Piwi 同源物作为候选干细胞(始原细胞)标志物。EfPiwiA mRNA 在具有始原细胞形态特征的细胞中表达。我们通过 BrdU 掺入表明这些表达 EfPiwiA 的细胞确实是干细胞,具有增殖能力,并通过 EfPiwiA 与推定定型始原细胞中的细胞谱系特异性基因的共表达证明其分化能力。EfPiwiA mRNA 表达在形成室的成熟领细胞中维持,与始原细胞分化为其他细胞类型时 EfPiwiA 基因表达向细胞谱系特异性标志物的转变形成对比。领细胞是具有与领鞭毛虫(微绒毛领和鞭毛)相似形态特征的食胞。它们在特定情况下转化为始原细胞并产生配子(主要是精子)的已知能力表明,即使它们完全分化,领细胞仍保持多能干细胞样潜能。基于 EfPiwiA 在始原细胞和领细胞中的特异性表达,结合以前的研究,我们提出始原细胞和领细胞都是海绵动物干细胞系统的组成部分。我们讨论了领细胞可能代表祖先干细胞,而始原细胞可能代表在祖先多细胞生物中进一步进化的干细胞的可能性。