A Rho signaling network links microtubules to PKD controlled carrier transport to focal adhesions

Abstract

Protein kinase D (PKD) is a family of serine/threonine kinases that is required for the structural integrity and function of the Golgi complex. Despite its importance in the regulation of Golgi function, the molecular mechanisms regulating PKD activity are still incompletely understood. Using the genetically encoded PKD activity reporter G-PKDrep we now uncover a Rho signaling network comprising GEF-H1, the RhoGAP DLC3, and the Rho effector PLCe that regulate the activation of PKD at trans-Golgi membranes. We further show that this molecular network coordinates the formation of TGN-derived Rab6-positive transport carriers delivering cargo for localized exocytosis at focal adhesions.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files.

Article and author information

Author details

  1. Stephan A Eisler

    Stuttgart Research Center Systems Biology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  2. Filipa Curado

    Institute of Cell Biology and Immunology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  3. Gisela Link

    Institute of Cell Biology and Immunology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  4. Sarah Schulz

    Institute of Cell Biology and Immunology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  5. Melanie Noack

    Stuttgart Research Center Systems Biology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  6. Maren Steinke

    Institute of Cell Biology and Immunology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  7. Monilola A Olayioye

    Stuttgart Research Center Systems Biology, University of Stuttgart, Stuttgart, Germany
    Competing interests
    The authors declare that no competing interests exist.
  8. Angelika Hausser

    Stuttgart Research Center Systems Biology, University of Stuttgart, Stuttgart, Germany
    For correspondence
    angelika.hausser@izi.uni-stuttgart.de
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-4102-9286

Funding

Deutsche Krebshilfe

  • Angelika Hausser

Deutsche Forschungsgemeinschaft

  • Angelika Hausser

Volkswagen Foundation

  • Angelika Hausser

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2018, Eisler et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 2,554
    views
  • 455
    downloads
  • 34
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Stephan A Eisler
  2. Filipa Curado
  3. Gisela Link
  4. Sarah Schulz
  5. Melanie Noack
  6. Maren Steinke
  7. Monilola A Olayioye
  8. Angelika Hausser
(2018)
A Rho signaling network links microtubules to PKD controlled carrier transport to focal adhesions
eLife 7:e35907.
https://doi.org/10.7554/eLife.35907

Share this article

https://doi.org/10.7554/eLife.35907

Further reading

    1. Cell Biology
    2. Developmental Biology
    Sofía Suárez Freire, Sebastián Perez-Pandolfo ... Mariana Melani
    Research Article

    Eukaryotic cells depend on exocytosis to direct intracellularly synthesized material toward the extracellular space or the plasma membrane, so exocytosis constitutes a basic function for cellular homeostasis and communication between cells. The secretory pathway includes biogenesis of secretory granules (SGs), their maturation and fusion with the plasma membrane (exocytosis), resulting in release of SG content to the extracellular space. The larval salivary gland of Drosophila melanogaster is an excellent model for studying exocytosis. This gland synthesizes mucins that are packaged in SGs that sprout from the trans-Golgi network and then undergo a maturation process that involves homotypic fusion, condensation, and acidification. Finally, mature SGs are directed to the apical domain of the plasma membrane with which they fuse, releasing their content into the gland lumen. The exocyst is a hetero-octameric complex that participates in tethering of vesicles to the plasma membrane during constitutive exocytosis. By precise temperature-dependent gradual activation of the Gal4-UAS expression system, we have induced different levels of silencing of exocyst complex subunits, and identified three temporarily distinctive steps of the regulated exocytic pathway where the exocyst is critically required: SG biogenesis, SG maturation, and SG exocytosis. Our results shed light on previously unidentified functions of the exocyst along the exocytic pathway. We propose that the exocyst acts as a general tethering factor in various steps of this cellular process.

    1. Cell Biology
    2. Developmental Biology
    Heungjin Ryu, Kibum Nam ... Jung-Hoon Park
    Research Article

    In most murine species, spermatozoa exhibit a falciform apical hook at the head end. The function of the sperm hook is not yet clearly understood. In this study, we investigate the role of the sperm hook in the migration of spermatozoa through the female reproductive tract in Mus musculus (C57BL/6), using a deep tissue imaging custom-built two-photon microscope. Through live reproductive tract imaging, we found evidence indicating that the sperm hook aids in the attachment of spermatozoa to the epithelium and facilitates interactions between spermatozoa and the epithelium during migration in the uterus and oviduct. We also observed synchronized sperm beating, which resulted from the spontaneous unidirectional rearrangement of spermatozoa in the uterus. Based on live imaging of spermatozoa-epithelium interaction dynamics, we propose that the sperm hook plays a crucial role in successful migration through the female reproductive tract by providing anchor-like mechanical support and facilitating interactions between spermatozoa and the female reproductive tract in the house mouse.