{"title":"ccl19 and ccl21 affect cell movements and differentiation in early Xenopus development","authors":"Toshiyasu Goto, Tatsuo Michiue, Hiroshi Shibuya","doi":"10.1111/dgd.12847","DOIUrl":null,"url":null,"abstract":"<p>We characterized <i>Xenopus laevis C-C motif chemokine ligand 19.L</i> (<i>ccl19.L</i>) and <i>C-C motif chemokine ligand 21.L</i> (<i>ccl21.L</i>) during early <i>Xenopus</i> embryogenesis. The temporal and spatial expression patterns of <i>ccl19.L</i> and <i>ccl21.L</i> tended to show an inverse correlation, except that the expression level was higher in the dorsal side at the gastrula stage. For example, even at the dorsal sector of the gastrulae, <i>ccl19.L</i> was expressed in the axial region and <i>ccl21.L</i> was expressed in the paraxial region. Dorsal overexpression of <i>ccl19.L</i> and <i>ccl21.L</i> and knockdown of Ccl19.L and Ccl21.L inhibited gastrulation, but their functions were different in cell behaviors during morphogenesis. Observation of Keller sandwich explants revealed that overexpression of both <i>ccl19.L</i> and <i>ccl21.L</i> and knockdown of Ccl21.L inhibited the convergent extension movements, while knockdown of Ccl19.L did not. <i>ccl19.L</i>-overexpressing explants attracted cells at a distance and <i>ccl21.L</i>-overexpressing explants attracted neighboring cells. Ventral overexpression of <i>ccl19.L</i> and <i>ccl21.L</i> induced secondary axis-like structures and <i>chrd.1</i> expression at the ventral side. Upregulation of <i>chrd.1</i> was induced by ligand mRNAs through <i>ccr7.S</i>. Knockdown of Ccl19.L and Ccl21.L inhibited gastrulation and downregulated <i>chrd.1</i> expression at the dorsal side. The collective findings indicate that <i>ccl19.L</i> and <i>ccl21.L</i> might play important roles in morphogenesis and dorsal–ventral patterning during early embryogenesis in <i>Xenopus</i>.</p>","PeriodicalId":50589,"journal":{"name":"Development Growth & Differentiation","volume":"65 3","pages":"175-189"},"PeriodicalIF":1.7000,"publicationDate":"2023-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development Growth & Differentiation","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/dgd.12847","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
We characterized Xenopus laevis C-C motif chemokine ligand 19.L (ccl19.L) and C-C motif chemokine ligand 21.L (ccl21.L) during early Xenopus embryogenesis. The temporal and spatial expression patterns of ccl19.L and ccl21.L tended to show an inverse correlation, except that the expression level was higher in the dorsal side at the gastrula stage. For example, even at the dorsal sector of the gastrulae, ccl19.L was expressed in the axial region and ccl21.L was expressed in the paraxial region. Dorsal overexpression of ccl19.L and ccl21.L and knockdown of Ccl19.L and Ccl21.L inhibited gastrulation, but their functions were different in cell behaviors during morphogenesis. Observation of Keller sandwich explants revealed that overexpression of both ccl19.L and ccl21.L and knockdown of Ccl21.L inhibited the convergent extension movements, while knockdown of Ccl19.L did not. ccl19.L-overexpressing explants attracted cells at a distance and ccl21.L-overexpressing explants attracted neighboring cells. Ventral overexpression of ccl19.L and ccl21.L induced secondary axis-like structures and chrd.1 expression at the ventral side. Upregulation of chrd.1 was induced by ligand mRNAs through ccr7.S. Knockdown of Ccl19.L and Ccl21.L inhibited gastrulation and downregulated chrd.1 expression at the dorsal side. The collective findings indicate that ccl19.L and ccl21.L might play important roles in morphogenesis and dorsal–ventral patterning during early embryogenesis in Xenopus.
期刊介绍:
Development Growth & Differentiation (DGD) publishes three types of articles: original, resource, and review papers.
Original papers are on any subjects having a context in development, growth, and differentiation processes in animals, plants, and microorganisms, dealing with molecular, genetic, cellular and organismal phenomena including metamorphosis and regeneration, while using experimental, theoretical, and bioinformatic approaches. Papers on other related fields are also welcome, such as stem cell biology, genomics, neuroscience, Evodevo, Ecodevo, and medical science as well as related methodology (new or revised techniques) and bioresources.
Resource papers describe a dataset, such as whole genome sequences and expressed sequence tags (ESTs), with some biological insights, which should be valuable for studying the subjects as mentioned above.
Submission of review papers is also encouraged, especially those providing a new scope based on the authors’ own study, or a summarization of their study series.