Section on Molecular Morphogenesis, Program in Cellular Regulation and Metabolism (PCRM), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, USA.
PLoS One. 2012;7(10):e47407. doi: 10.1371/journal.pone.0047407. Epub 2012 Oct 10.
The formation and/or maturation of adult organs in vertebrates often takes place during postembryonic development, a period around birth in mammals when thyroid hormone (T3) levels are high. The T3-dependent anuran metamorphosis serves as a model to study postembryonic development. Studies on the remodeling of the intestine during Xenopus (X.) laevis metamorphosis have shown that the development of the adult intestine involves de novo formation of adult stem cells in a process controlled by T3. On the other hand, X. tropicalis, highly related to X. laevis, offers a number of advantages for studying developmental mechanisms, especially at genome-wide level, over X. laevis, largely due to its shorter life cycle and sequenced genome. To establish X. tropicalis intestinal metamorphosis as a model for adult organogenesis, we analyzed the morphological and cytological changes in X. tropicalis intestine during metamorphosis.
METHODOLOGY/PRINCIPAL FINDINGS: We observed that in X. tropicalis, the premetamorphic intestine was made of mainly a monolayer of larval epithelial cells surrounded by little connective tissue except in the single epithelial fold, the typhlosole. During metamorphosis, the larval epithelium degenerates and adult epithelium develops to form a multi-folded structure with elaborate connective tissue and muscles. Interestingly, typhlosole, which is likely critical for adult epithelial development, is present along the entire length of the small intestine in premetamorphic tadpoles, in contrast to X. laevis, where it is present only in the anterior 1/3. T3-treatment induces intestinal remodeling, including the shortening of the intestine and the typhlosole, just like in X. laevis.
CONCLUSIONS/SIGNIFICANCE: Our observations indicate that the intestine undergoes similar metamorphic changes in X. laevis and X. tropicalis, making it possible to use the large amount of information available on X. laevis intestinal metamorphosis and the genome sequence information and genetic advantages of X. tropicalis to dissect the pathways governing adult intestinal development.
脊椎动物的成年器官的形成和/或成熟通常发生在胚胎后发育期间,这是哺乳动物出生前后的一个时期,此时甲状腺激素 (T3) 水平较高。依赖 T3 的蛙类变态发育是研究胚胎后发育的模型。在非洲爪蟾(X. laevis)变态发育过程中对肠道重塑的研究表明,成年肠道的发育涉及到 T3 控制的新形成的成年干细胞。另一方面,与 X. laevis 高度相关的 X. tropicalis 在研究发育机制方面提供了许多优势,尤其是在全基因组水平上,这在很大程度上归因于其较短的生命周期和已测序的基因组。为了将 X. tropicalis 肠道变态发育确立为成年器官发生的模型,我们分析了 X. tropicalis 肠道在变态发育过程中的形态和细胞学变化。
方法/主要发现:我们观察到,在 X. tropicalis 中,前变态期肠道主要由一层幼虫上皮细胞组成,除了单个上皮褶皱——幽门瓣外,周围只有少量的结缔组织。在变态期间,幼虫上皮细胞退化,成年上皮细胞发育形成具有精细结缔组织和肌肉的多褶皱结构。有趣的是,幽门瓣对于成年上皮细胞的发育可能至关重要,它存在于前变态期幼体的整个小肠中,而在 X. laevis 中,它仅存在于前 1/3 处。T3 处理诱导肠道重塑,包括肠道和幽门瓣的缩短,这与 X. laevis 相似。
结论/意义:我们的观察表明,X. laevis 和 X. tropicalis 的肠道经历了相似的变态变化,这使得利用 X. laevis 肠道变态发育的大量可用信息以及 X. tropicalis 的基因组序列信息和遗传优势来剖析控制成年肠道发育的途径成为可能。