Literature DB >> 28994799

The C. elegans Intestine As a Model for Intercellular Lumen Morphogenesis and In Vivo Polarized Membrane Biogenesis at the Single-cell Level: Labeling by Antibody Staining, RNAi Loss-of-function Analysis and Imaging.

Nan Zhang1, Liakot A Khan2, Edward Membreno2, Gholamali Jafari2, Siyang Yan2, Hongjie Zhang3, Verena Gobel4.   

Abstract

Multicellular tubes, fundamental units of all internal organs, are composed of polarized epithelial or endothelial cells, with apical membranes lining the lumen and basolateral membranes contacting each other and/or the extracellular matrix. How this distinctive membrane asymmetry is established and maintained during organ morphogenesis is still an unresolved question of cell biology. This protocol describes the C. elegans intestine as a model for the analysis of polarized membrane biogenesis during tube morphogenesis, with emphasis on apical membrane and lumen biogenesis. The C. elegans twenty-cell single-layered intestinal epithelium is arranged into a simple bilaterally symmetrical tube, permitting analysis on a single-cell level. Membrane polarization occurs concomitantly with polarized cell division and migration during early embryogenesis, but de novo polarized membrane biogenesis continues throughout larval growth, when cells no longer proliferate and move. The latter setting allows one to separate subcellular changes that simultaneously mediate these different polarizing processes, difficult to distinguish in most polarity models. Apical-, basolateral membrane-, junctional-, cytoskeletal- and endomembrane components can be labeled and tracked throughout development by GFP fusion proteins, or assessed by in situ antibody staining. Together with the organism's genetic versatility, the C. elegans intestine thus provides a unique in vivo model for the visual, developmental, and molecular genetic analysis of polarized membrane and tube biogenesis. The specific methods (all standard) described here include how to: label intestinal subcellular components by antibody staining; analyze genes involved in polarized membrane biogenesis by loss-of-function studies adapted to the typically essential tubulogenesis genes; assess polarity defects during different developmental stages; interpret phenotypes by epifluorescence, differential interference contrast (DIC) and confocal microscopy; quantify visual defects. This protocol can be adapted to analyze any of the often highly conserved molecules involved in epithelial polarity, membrane biogenesis, tube and lumen morphogenesis.

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Year:  2017        PMID: 28994799      PMCID: PMC5628585          DOI: 10.3791/56100

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


  38 in total

1.  Organogenesis of the Caenorhabditis elegans intestine.

Authors:  B Leung; G J Hermann; J R Priess
Journal:  Dev Biol       Date:  1999-12-01       Impact factor: 3.582

Review 2.  Adaptation of core mechanisms to generate cell polarity.

Authors:  W James Nelson
Journal:  Nature       Date:  2003-04-17       Impact factor: 49.962

Review 3.  Epithelial polarity and tubulogenesis in vitro.

Authors:  Mirjam M P Zegers; Lucy E O'Brien; Wei Yu; Anirban Datta; Keith E Mostov
Journal:  Trends Cell Biol       Date:  2003-04       Impact factor: 20.808

Review 4.  The art and design of genetic screens: caenorhabditis elegans.

Authors:  Erik M Jorgensen; Susan E Mango
Journal:  Nat Rev Genet       Date:  2002-05       Impact factor: 53.242

5.  Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans.

Authors:  L Timmons; D L Court; A Fire
Journal:  Gene       Date:  2001-01-24       Impact factor: 3.688

6.  Loss of the putative RNA-directed RNA polymerase RRF-3 makes C. elegans hypersensitive to RNAi.

Authors:  Femke Simmer; Marcel Tijsterman; Susan Parrish; Sandhya P Koushika; Michael L Nonet; Andrew Fire; Julie Ahringer; Ronald H A Plasterk
Journal:  Curr Biol       Date:  2002-08-06       Impact factor: 10.834

7.  A conserved siRNA-degrading RNase negatively regulates RNA interference in C. elegans.

Authors:  Scott Kennedy; Duo Wang; Gary Ruvkun
Journal:  Nature       Date:  2004-02-12       Impact factor: 49.962

8.  Genome-wide RNAi screening in Caenorhabditis elegans.

Authors:  Ravi S Kamath; Julie Ahringer
Journal:  Methods       Date:  2003-08       Impact factor: 3.608

9.  Systematic functional analysis of the Caenorhabditis elegans genome using RNAi.

Authors:  Ravi S Kamath; Andrew G Fraser; Yan Dong; Gino Poulin; Richard Durbin; Monica Gotta; Alexander Kanapin; Nathalie Le Bot; Sergio Moreno; Marc Sohrmann; David P Welchman; Peder Zipperlen; Julie Ahringer
Journal:  Nature       Date:  2003-01-16       Impact factor: 49.962

10.  Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans.

Authors:  R S Kamath; M Martinez-Campos; P Zipperlen; A G Fraser; J Ahringer
Journal:  Genome Biol       Date:  2000-12-20       Impact factor: 13.583

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  2 in total

1.  The C. elegans Excretory Canal as a Model for Intracellular Lumen Morphogenesis and In Vivo Polarized Membrane Biogenesis in a Single Cell: labeling by GFP-fusions, RNAi Interaction Screen and Imaging.

Authors:  Nan Zhang; Edward Membreno; Susan Raj; Hongjie Zhang; Liakot A Khan; Verena Gobel
Journal:  J Vis Exp       Date:  2017-10-03       Impact factor: 1.355

2.  A tensile trilayered cytoskeletal endotube drives capillary-like lumenogenesis.

Authors:  Liakot A Khan; Gholamali Jafari; Nan Zhang; Edward Membreno; Siyang Yan; Hongjie Zhang; Verena Gobel
Journal:  J Cell Biol       Date:  2019-06-25       Impact factor: 10.539

  2 in total

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