Literature DB >> 25867882

Upright imaging of Drosophila egg chambers.

Lathiena Manning1, Michelle Starz-Gaiano2.   

Abstract

Drosophila melanogaster oogenesis provides an ideal context for studying varied developmental processes since the ovary is relatively simple in architecture, is well-characterized, and is amenable to genetic analysis. Each egg chamber consists of germ-line cells surrounded by a single epithelial layer of somatic follicle cells. Subsets of follicle cells undergo differentiation during specific stages to become several different cell types. Standard techniques primarily allow for a lateral view of egg chambers, and therefore a limited view of follicle cell organization and identity. The upright imaging protocol describes a mounting technique that enables a novel, vertical view of egg chambers with a standard confocal microscope. Samples are first mounted between two layers of glycerin jelly in a lateral (horizontal) position on a glass microscope slide. The jelly with encased egg chambers is then cut into blocks, transferred to a coverslip, and flipped to position egg chambers upright. Mounted egg chambers can be imaged on either an upright or an inverted confocal microscope. This technique enables the study of follicle cell specification, organization, molecular markers, and egg development with new detail and from a new perspective.

Entities:  

Mesh:

Year:  2015        PMID: 25867882      PMCID: PMC4401243          DOI: 10.3791/52636

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


  24 in total

1.  Intercellular protein movement in syncytial Drosophila follicle cells.

Authors:  Stephanie J Airoldi; Peter F McLean; Yuko Shimada; Lynn Cooley
Journal:  J Cell Sci       Date:  2011-12-01       Impact factor: 5.285

2.  Exploring strategies for protein trapping in Drosophila.

Authors:  Ana T Quiñones-Coello; Lisa N Petrella; Kathleen Ayers; Anthony Melillo; Stacy Mazzalupo; Andrew M Hudson; Shu Wang; Claudia Castiblanco; Michael Buszczak; Roger A Hoskins; Lynn Cooley
Journal:  Genetics       Date:  2006-12-18       Impact factor: 4.562

3.  The JAK/STAT pathway is required for border cell migration during Drosophila oogenesis.

Authors:  Simone Beccari; Luís Teixeira; Pernille Rørth
Journal:  Mech Dev       Date:  2002-02       Impact factor: 1.882

4.  The Drosophila cytokine receptor Domeless controls border cell migration and epithelial polarization during oogenesis.

Authors:  Christian Ghiglione; Olivier Devergne; Emmanuelle Georgenthum; Fabrice Carballès; Caroline Médioni; Delphine Cerezo; Stéphane Noselli
Journal:  Development       Date:  2002-12       Impact factor: 6.868

5.  Glypicans regulate JAK/STAT signaling and distribution of the Unpaired morphogen.

Authors:  Yoshiki Hayashi; Travis R Sexton; Katsufumi Dejima; Dustin W Perry; Masahiko Takemura; Satoru Kobayashi; Hiroshi Nakato; Douglas A Harrison
Journal:  Development       Date:  2012-11       Impact factor: 6.868

Review 6.  Methods for studying oogenesis.

Authors:  Andrew M Hudson; Lynn Cooley
Journal:  Methods       Date:  2014-01-17       Impact factor: 3.608

7.  A gradient of JAK pathway activity patterns the anterior-posterior axis of the follicular epithelium.

Authors:  Rongwen Xi; Jennifer R McGregor; Douglas A Harrison
Journal:  Dev Cell       Date:  2003-02       Impact factor: 12.270

Review 8.  Group choreography: mechanisms orchestrating the collective movement of border cells.

Authors:  Denise J Montell; Wan Hee Yoon; Michelle Starz-Gaiano
Journal:  Nat Rev Mol Cell Biol       Date:  2012-10       Impact factor: 94.444

Review 9.  Patterning: JAK-STAT signalling in the Drosophila follicular epithelium.

Authors:  Natalie Denef; Trudi Schüpbach
Journal:  Curr Biol       Date:  2003-05-13       Impact factor: 10.834

Review 10.  Border-cell migration: the race is on.

Authors:  Denise J Montell
Journal:  Nat Rev Mol Cell Biol       Date:  2003-01       Impact factor: 94.444

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.