Howard Hughes Medical Institute and Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Dev Cell. 2012 Oct 16;23(4):691-704. doi: 10.1016/j.devcel.2012.09.008.
Planarians grow and regenerate organs by coordinating proliferation and differentiation of pluripotent stem cells with remodeling of postmitotic tissues. Understanding how these processes are orchestrated requires characterizing cell-type-specific gene expression programs and their regulation during regeneration and homeostasis. To this end, we analyzed the expression profile of planarian intestinal phagocytes, cells responsible for digestion and nutrient storage/distribution. Utilizing RNA interference, we identified cytoskeletal regulators required for intestinal branching morphogenesis and a modulator of bioactive sphingolipid metabolism, ceramide synthase, required for the production of functional phagocytes. Additionally, we found that a gut-enriched homeobox transcription factor, nkx-2.2, is required for somatic stem cell proliferation, suggesting a niche-like role for phagocytes. Identification of evolutionarily conserved regulators of intestinal branching, differentiation, and stem cell dynamics demonstrates the utility of the planarian digestive system as a model for elucidating the mechanisms controlling postembryonic organogenesis.
涡虫通过协调多能干细胞的增殖和分化与有丝分裂后组织的重塑来生长和再生器官。了解这些过程是如何协调的,需要对细胞类型特异性基因表达程序及其在再生和稳态过程中的调控进行特征描述。为此,我们分析了涡虫肠道吞噬细胞的表达谱,这些细胞负责消化和营养物质的储存/分布。利用 RNA 干扰,我们鉴定了肠道分支形态发生所必需的细胞骨架调节剂,以及生物活性神经酰胺代谢调节剂,即神经酰胺合酶,它对于功能性吞噬细胞的产生是必需的。此外,我们发现肠道富集的同源盒转录因子 nkx-2.2 对于体干细胞的增殖是必需的,这表明吞噬细胞具有类似小生境的作用。鉴定出进化上保守的肠道分支、分化和干细胞动力学的调控因子,证明了涡虫消化系统作为阐明控制胚胎后器官发生机制的模型的实用性。