Sec24-Dependent Secretion Drives Cell-Autonomous Expansion of Tracheal Tubes in Drosophila

Autor: Dominique Förster, Kristina Armbruster, Stefan Luschnig
Přispěvatelé: University of Zurich, Luschnig, S
Rok vydání: 2010
Předmět:
Male
Protein subunit
Recombinant Fusion Proteins
Cell
Green Fluorescent Proteins
Vesicular Transport Proteins
Genes
Insect

DEVBIO
1100 General Agricultural and Biological Sciences
Matrix (biology)
Biology
medicine.disease_cause
General Biochemistry
Genetics and Molecular Biology

Animals
Genetically Modified

03 medical and health sciences
0302 clinical medicine
Microscopy
Electron
Transmission

1300 General Biochemistry
Genetics and Molecular Biology

medicine
Animals
Drosophila Proteins
Secretion
COPII
Process (anatomy)
030304 developmental biology
0303 health sciences
Mutation
Agricultural and Biological Sciences(all)
Base Sequence
Biochemistry
Genetics and Molecular Biology(all)

Anatomy
Apical membrane
10124 Institute of Molecular Life Sciences
Cell biology
Trachea
medicine.anatomical_structure
Mutagenesis
Site-Directed

570 Life sciences
biology
Drosophila
Female
CELLBIO
General Agricultural and Biological Sciences
030217 neurology & neurosurgery
Zdroj: Europe PubMed Central
Current biology : CB
DOI: 10.5167/uzh-28846
Popis: SummaryEpithelial tubes in developing organs, such as mammalian lungs and insect tracheae, need to expand their initially narrow lumina to attain their final, functional dimensions [1]. Despite its critical role for organ function, the cellular mechanism of tube expansion remains unclear. Tracheal tube expansion in Drosophila involves apical secretion and deposition of a luminal matrix [2–5], but the mechanistic role of secretion and the nature of forces involved in the process were not previously clear. Here we address the roles of cell-intrinsic and extrinsic processes in tracheal tube expansion. We identify mutations in the sec24 gene stenosis, encoding a cargo-binding subunit of the COPII complex [6–8]. Via genetic-mosaic analyses, we show that stenosis-dependent secretion drives tube expansion in a cell-autonomous fashion. Strikingly, single cells autonomously adjust both tube diameter and length by implementing a sequence of events including apical membrane growth, cell flattening, and taenidial cuticle formation. Known luminal components are not required for this process. Thus, a cell-intrinsic program, rather than nonautonomous extrinsic cues, controls the dimensions of tracheal tubes. These results indicate a critical role of membrane-associated proteins in the process and imply a mechanism that coordinates autonomous behaviors of individual cells within epithelial structures.
Databáze: OpenAIRE