FP7Reintegration grant2011–2013

GSL in development · The role of glycosphingolipids in development

FP7 — People (Marie Curie Actions)

Duration
2011-03-01 → 2013-09-30
EU contribution
€62,500
Participants
1
Scheme
MC-IRG

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Results in brief

The role of glycosphingolipids in development

Introduction: The initial aim of our project was to understand the role of glycosphingolipids in development. During the course of this study, we have identified that one of the enzyme involved in the synthesis of core glycosphingolipids, brainiac (brn), was important in the biology of the stem cell niche of the testis in Drosophila melanogaster males. Indeed, these males presented an abnormal maintenance of the stem cells forming their testis niche. This seminal finding led us to focus more precisely on the testis stem cell niche homeostasis in order to understand with precision what could be the influence of brn in the signalling network underlying the regulation of the maintenance and the activity of the testis stem cell niche. The testis stem cell niche is localized at the apical tip of the testis and formed by three main populations of cells. Some post-differentiated cells, the hub cells (HC), form together a structure displaying a hub architecture around which are anchored two populations of stem cells: the germ stem cells (GSC) which give rise to the sperm and the somatic stem cells (SSC). SSC give rise to cyst cells that accompany and support GSC over spermatogenesis and can replenish HC over age. In addition, both HC and SSC can participate to the maintenance and the regulation of the activity of GSC. The relative contribution of SSC and hub cells to GSC regulation remains however a matter of debate. Finally, GSC can control SSC differentiation. Hence given the tight functional relationship existing between HC, SSC and GSC, we have decided in our work to consider that all these three populations of cells form the testis stem cell niche. Results: In order to describe quantitatively the functional state of the testis stem cell niche, we have developed a novel analytical approach consisting in first, counting precisely each of the cell populations forming the testis niche by taking advantage of our ability to identify all HC, SSC and GSC cells; second, applying a Pearson correlation matrix analysis to these data in order to describe the existence of any correlation between two cellular populations at the single testis level. High correlation values between two cellular populations, HC and GSC for example, can indeed be interpreted as a functional niche interaction between these two types of cells. By using this strategy, we have been able to describe quantitatively the variation and the dynamic of the activity of the testis stem cell niche in various environmental and physiological conditions, in other words the phenotypic plasticity of the testis stem cell niche. Importantly, during this characterization, we realized that Wolbachia pipientis, an alphaproteobacteria, which is a natural endosymbiont of D melanogaster in the wild, affected significantly the testis niche homeostasis. By precisely analyzing the influence of this bacteria on the homeostasis of the testis stem cell niche in wild type males, we have demonstrated that Wolbachia pipientis likely affected the relative contribution of HC and SSC to GSC maintenance. In addition, the infection by the bacteria was associated to a better maintenance of both somatic and germinal stem cells during the aging of Wolbachia-infected males. These results suggest that Wolbachia infection might promote a better fitness of the infected males. This manuscript is currently in revision. Conclusions and Impact of the work: The homeostasis of self-renewing tissues is dependent on the appropriate regulation of stem cells by their microenvironment. Understanding how environmental and physiological changes impact on the activity of stem cells is a key issue. During our IRG granting period, we studied the impact of such changes on the stem cells of the Drosophila testis. Our study has allowed us to highlight the high degree of phenotypic plasticity of this niche and to provide a useful analytical framework to study in the future the impacts of environmental, physiological and genetic perturbations on the homeostasis of a stem cell niche. Our work has in addition unveiled a previously unknown impact of the Wolbachia endosymbiont on Drosophila testis niche. Wolbachia pipientis is a common endosymbiont in many different arthropod and worm species on the planet. Recently, Wolbachia has become became famous for conferring a resistance of its host to many different parasites and virus, among which those responsible for Malaria and the lethal Dengue fever. By opening a new window on the impact of Wolbachia on the physiology and the tissue homeostasis of its hosts, our work, will hopefully inspire new research avenues allowing the scientific community to understand how this bacteria manipulates the immune system of its hosts and fortunately impair their ability to spread lethal human pandemic diseases.

Data: CORDIS, © European Union

Project objective

Glycosphingolipids have been implicated in the development of various human pathologies, such as cancer, obesity, diabetes or Alzheimer diseases. Their wide implication in cellular membrane architecture and cellular signaling network and metabolism has however made difficult the establishment of an integrated and accurate understanding of their role in vivo. The current proposal aims to understand such a role by taking advantage of a highly versatile system model, the Drosophila melanogaster. By combining sophisticated genetic and biochemical approaches with cutting edge biophysical strategies, such as FRET or FRAP technologies, this proposal intends to 1) determine how GSLs affect the dynamic organization of membranes at the nanoscale resolution in vivo, 2) study the GSL impact on cellular signaling and 3) polarity and finally 4) uncover some putative molecular regulators of GSL function in vivo. Preliminary work in Drosophila embryos allowed us to demonstrate that the absence of core GSLs in two related lethal mutants, egghead (egh) and brainiac (brn), leads to a surprisingly specific phenotype consisting in an increased number of proprioceptive organs. During the eclosion process, flies lacking core GSLs are unable to organize their movements and dies within the pupae case. Interestingly, Brn protein expression in brn flies using the UAS/GAL4 system in proprioception organs rescues their phenotype. We hence intend to take advantage of these rescue conditions to screen for molecular factors allowing to compensate the absence of core GSLs. Finally, the increased in proprioceptive organs being typically associated to an upregulation of the EGFR pathway, we aim to understand its genetic relationship of brn and egh mutations. This comprehensive characterization of the role of core GSLs in vivo will certainly constitute an important step in order to further evaluate the nature of their function in Drosophila models of human diseases in the near future.

Original text from CORDIS.

Participants

  • INSTITUT PASTEUR · ParisCoordinatorFrance

Links

Data: CORDIS, © European Union