Literature DB >> 27341538

Generation of Parabiotic Zebrafish Embryos by Surgical Fusion of Developing Blastulae.

Elliott J Hagedorn1, Jennifer L Cillis2, Caitlyn R Curley2, Taylor C Patch2, Brian Li1, Bradley W Blaser3, Raquel Riquelme1, Leonard I Zon4, Dhvanit I Shah5.   

Abstract

Surgical parabiosis of two animals of different genetic backgrounds creates a unique scenario to study cell-intrinsic versus cell-extrinsic roles for candidate genes of interest, migratory behaviors of cells, and secreted signals in distinct genetic settings. Because parabiotic animals share a common circulation, any blood or blood-borne factor from one animal will be exchanged with its partner and vice versa. Thus, cells and molecular factors derived from one genetic background can be studied in the context of a second genetic background. Parabiosis of adult mice has been  used extensively to research aging, cancer, diabetes, obesity, and brain development. More recently, parabiosis of zebrafish embryos has been used to study the developmental biology of hematopoiesis. In contrast to mice, the transparent nature of zebrafish embryos permits the direct visualization of cells in the parabiotic context, making it a uniquely powerful method for investigating fundamental cellular and molecular mechanisms. The utility of this technique, however, is limited by a steep learning curve for generating the parabiotic zebrafish embryos. This protocol provides a step-by-step method on how to surgically fuse the blastulae of two zebrafish embryos of different genetic backgrounds to investigate the role of candidate genes of interest. In addition, the parabiotic zebrafish embryos are tolerant to heat shock, making temporal control of gene expression possible. This method does not require a sophisticated set-up and has broad applications for studying cell migration, fate specification, and differentiation in vivo during embryonic development.

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Year:  2016        PMID: 27341538      PMCID: PMC4927786          DOI: 10.3791/54168

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  20 in total

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4.  Quail-chick chimaeras and parabionts: several new models to investigate early developmental events in the haemopoietic system [proceedings].

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Authors:  E M Morin-Kensicki; C Faust; C LaMantia; T Magnuson
Journal:  Genesis       Date:  2001-12       Impact factor: 2.487

6.  NACA deficiency reveals the crucial role of somite-derived stromal cells in haematopoietic niche formation.

Authors:  Emi Murayama; Milka Sarris; Michael Redd; Dorothée Le Guyader; Catherine Vivier; Wyatt Horsley; Nikolaus Trede; Philippe Herbomel
Journal:  Nat Commun       Date:  2015-09-28       Impact factor: 14.919

7.  Parabiosis in mice: a detailed protocol.

Authors:  Paniz Kamran; Konstantina-Ioanna Sereti; Peng Zhao; Shah R Ali; Irving L Weissman; Reza Ardehali
Journal:  J Vis Exp       Date:  2013-10-06       Impact factor: 1.355

8.  Cell-autonomous and non-autonomous requirements for the zebrafish gene cloche in hematopoiesis.

Authors:  L Parker; D Y Stainier
Journal:  Development       Date:  1999-06       Impact factor: 6.868

9.  Hematopoietic stem cell arrival triggers dynamic remodeling of the perivascular niche.

Authors:  Owen J Tamplin; Ellen M Durand; Logan A Carr; Sarah J Childs; Elliott J Hagedorn; Pulin Li; Amanda D Yzaguirre; Nancy A Speck; Leonard I Zon
Journal:  Cell       Date:  2015-01-15       Impact factor: 41.582

10.  Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts.

Authors:  Dhvanit I Shah; Naoko Takahashi-Makise; Jeffrey D Cooney; Liangtao Li; Iman J Schultz; Eric L Pierce; Anupama Narla; Alexandra Seguin; Shilpa M Hattangadi; Amy E Medlock; Nathaniel B Langer; Tamara A Dailey; Slater N Hurst; Danilo Faccenda; Jessica M Wiwczar; Spencer K Heggers; Guillaume Vogin; Wen Chen; Caiyong Chen; Dean R Campagna; Carlo Brugnara; Yi Zhou; Benjamin L Ebert; Nika N Danial; Mark D Fleming; Diane M Ward; Michelangelo Campanella; Harry A Dailey; Jerry Kaplan; Barry H Paw
Journal:  Nature       Date:  2012-11-07       Impact factor: 49.962

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  5 in total

1.  Smarca5-mediated epigenetic programming facilitates fetal HSPC development in vertebrates.

Authors:  Yanyan Ding; Wen Wang; Dongyuan Ma; Guixian Liang; Zhixin Kang; Yuanyuan Xue; Yifan Zhang; Lu Wang; Jian Heng; Yong Zhang; Feng Liu
Journal:  Blood       Date:  2021-01-14       Impact factor: 22.113

Review 2.  Efforts to enhance blood stem cell engraftment: Recent insights from zebrafish hematopoiesis.

Authors:  Julie R Perlin; Anne L Robertson; Leonard I Zon
Journal:  J Exp Med       Date:  2017-08-22       Impact factor: 14.307

3.  CXCR1 remodels the vascular niche to promote hematopoietic stem and progenitor cell engraftment.

Authors:  Bradley W Blaser; Jessica L Moore; Elliott J Hagedorn; Brian Li; Raquel Riquelme; Asher Lichtig; Song Yang; Yi Zhou; Owen J Tamplin; Vera Binder; Leonard I Zon
Journal:  J Exp Med       Date:  2017-03-28       Impact factor: 14.307

4.  Quality assurance of hematopoietic stem cells by macrophages determines stem cell clonality.

Authors:  Samuel J Wattrus; Mackenzie L Smith; Cecilia Pessoa Rodrigues; Elliott J Hagedorn; Ji Wook Kim; Bogdan Budnik; Leonard I Zon
Journal:  Science       Date:  2022-09-22       Impact factor: 63.714

5.  The chromatin-remodeling enzyme Smarca5 regulates erythrocyte aggregation via Keap1-Nrf2 signaling.

Authors:  Yanyan Ding; Yuzhe Li; Ziqian Zhao; Qiangfeng Cliff Zhang; Feng Liu
Journal:  Elife       Date:  2021-10-26       Impact factor: 8.140

  5 in total

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