Image shows Neural Stem Cells (green, GFP) inside the Drosophila brain, some about to divide (red, CyclinB).

Courtesy of Claudia
Barros Lab

Image shows Neural Stem Cells (green, GFP) inside the Drosophila brain, some about to divide (red, CyclinB). Courtesy of Claudia Barros Lab

Postnatal neurogenesis promotes brain plasticity and function. Intrinsic and extrinsic signals converge to promote appropriate postembryonic NSC development and maintenance. Restricting NSC potential is equally vital as the expansion of aberrant neural stem-like cells can lead to brain tumour growth.
Our main goal is to identify fundamental intrinsic Neural Stem Cell (NSC) properties and extrinsic niche signals regulating the pace of postembryonic neurogenesis in both health and in disease, such as upon neoplastic transformation. We use a well-known genetically tractable in vivo model – the fruit fly Drosophila brain – and translate findings into mammalian systems, as well as human brain samples.
Current projects in the laboratory address three major questions in NSC biology:
Courtesy of Claudia
Barros Lab
Courtesy of Claudia Barros Lab
Q1: How do NSCs transit from a quiescent to a mitotically active state?
As in mammals, Drosophila postembryonic NSCs transit from quiescence to a mitotically active state to generate adult brain neurons and glia. The mechanisms underlying NSC mitotic reactivation remain largely unknown. We are screening and characterising the role of genes involved in this process using Drosophila, and aim at investigating conserved functions in mammalian systems.
Q2: How is the identity of different NSCs established?
It is becoming increasingly clear that the developing and adult mammalian brain harbours distinct NSC types. Yet, information about their molecular identity is currently at its infancy. The identification of different NSC types in the Drosophila larval brain, the evolutionary conservation of regulatory mechanisms, and the genetic tools available prompted us to use Drosophila as a model to identify novel NSC type-specific molecular properties that may be conserved in mammals.
Q3: What are the key mechanisms responsible for the transformation of normal NSC lineage cells into brain tumour-initiation cells?
Cells with NSC-like characteristics exist within brain tumours and can reform whole tumour masses. These so-called brain cancer stem cells are thought to originate from de-differentiation and/or transformation of normal NSC lineage cells. Using a Drosophila brain tumour model, we are screening and characterising genes potentially involved in molecular changes leading to brain tumour initiation and growth. We translate our findings into mammalian systems, including patient-derived brain cancer stem cells and human brain tumour tissues.
Prospective students or staff interested in joining our group, please contact Dr Claudia Barros.

Current lab members

Claudia Barros Lab team

Lab celebrations

  • April 2017: Congratulations to Laura Rodriguez-Diaz for her first-place poster prize at the Annual Plymouth PSMD postgraduate research conference.
  • October 2016: Congratulations to Karolina Jaworek for her PhD degree.
  • October 2014: Funding for better understanding of neural stem cells.
Neural Stem Cell
lineages (green) in the Drosophila Brain
Image shows neural stem cell lineages (green) in the Drosophila brain

Alumni and next destinations:

  • Jamie Pugh (PhD, 2023), Medical Writer, Oxford PharmaGenesis
  • Nsikan Nsek (PhD viva 2024), postdoctoral researcher, MRC Laboratory of Medical Sciences, London, UK
  • Laura Rodriguez Diaz (PhD 2016–20), Scientist, Theolytics Biotech, Oxford, UK
  • Eleanor Gonzaga (PhD 2013–16, 2018–19), Postdoctoral Research Associate, University of Cambridge, UK
  • Karolina Jaworek (PhD 2012–16), Postdoctoral Research Associate, University of Exeter, UK
  • Annabelle Mufti (2023-24), Paula Varney (2017–18), Joao Marques (2015–16), Eleni Costa (2015–16) and Oliver Warrington (2014–15) – one-year research undergraduates
  • Matthew Sherwood (Postgraduate research placement, May–September 2017), PhD student, University of Southampton, UK
  • Eleanor Gonzaga (MRes 2013–14, PhD University of Plymouth) and Helena Robinson (MRes 2013–14, PhD Bangor University UK)
  • Thomas Hughes (2015), Joshua Lewis (2016) and Chelsey Wiley (2017) – MSc students
  • Hubert Bieluczyk (Research Assistant, February–September 2018), Data Scientist, Legal & General, UK


  • Diaz LR, Gil-Ranedo J, Jaworek KJ, Nsek N, Marques JP, Costa E, Hilton DA, Bieluczyk H, Warrington O, Hanemann CO, Futschik ME, Bossing T & Barros CS (2024). Ribogenesis boosts controlled by HEATR1-MYC interplay promote transition into brain tumour growth. EMBO Reports Jan;25(1):168-197, DOI PEARL
  • Barros CS & Bossing T (2021) 'Microtubule disruption upon CNS damage triggers mitotic entry via TNF signaling activation' Cell Reports 36, (1), DOI Open access
  • Gil-Ranedo J, Gonzaga E, Jaworek KJ, Berger C, Bossing T & Barros CS (2019) 'STRIPAK Members Orchestrate Hippo and Insulin Receptor Signaling to Promote Neural Stem Cell Reactivation' Cell Reports 27, (10) 2921-2933.e5, DOI PEARL
  • Raghu SV, Mohammad F, Chua JY, Lam JSW, Loberas M, Sahani S, Barros CS & Claridge-Chang A 2018 'A zinc-finger fusion protein refines Gal4-defined neural circuits' Molecular Brain 11, (1) 46-46 Author Site, DOI PEARL
  • Xu J, Hartley BJ, Kurup P, Phillips A, Topol A, Xu M, Ononenyi C, Foscue E, Ho S-M & Baguley TD 2016 'Inhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia models' Molecular Psychiatry, DOI PEARL
  • Ding R, Weynans K, Bossing T, Barros CS & Berger C 2016 'The Hippo signalling pathway maintains quiescence in Drosophila neural stem cells' Nature Communications 7, 10510-10510, DOI PEARL
  • Cahill ME, Jones KA, Rafalovich I, Xie Z, Barros CS, Müller U & Penzes P 2012 'Control of interneuron dendritic growth through NRG1/erbB4-mediated kalirin-7 disinhibition' Mol Psychiatry 17, (1) 1-107 Author Site, DOI PEARL
  • Bossing T, Barros CS, Fischer B, Russell S & Shepherd D 2012 'Disruption of microtubule integrity initiates mitosis during CNS repair' Dev Cell 23, (2) 433-440 Author Site, DOI PEARL
  • Barros CS, Franco SJ & Müller U 2011 'Extracellular matrix: functions in the nervous system' Cold Spring Harb Perspect Biol 3, (1) Author Site, DOI PEARL
  • Barros CS, Nguyen T, Spencer KSR, Nishiyama A, Colognato H & Müller U 2009 'Beta1 integrins are required for normal CNS myelination and promote AKT-dependent myelin outgrowth' Development 136, (16) 2717-2724 Author Site, DOI PEARL
  • Barros CS, Calabrese B, Chamero P, Roberts AJ, Korzus E, Lloyd K, Stowers L, Mayford M, Halpain S & Müller U 2009 'Impaired maturation of dendritic spines without disorganization of cortical cell layers in mice lacking NRG1/ErbB signaling in the central nervous system' Proc Natl Acad Sci U S A 106, (11) 4507-4512 Author Site, DOI PEARL
  • Radakovits R, Barros CS, Belvindrah R, Patton B & Müller U 2009 'Regulation of radial glial survival by signals from the meninges' J Neurosci 29, (24) 7694-7705 Author Site, DOI PEARL
  • Barros CS, Phelps CB & Brand AH 2003 'Drosophila nonmuscle myosin II promotes the asymmetric segregation of cell fate determinants by cortical exclusion rather than active transport' Dev Cell 5, (6) 829-840 Author Site PEARL
  • Bossing T, Barros CS & Brand AH 2002 'Rapid tissue-specific expression assay in living embryos' Genesis 34, (1-2) 123-126 Author Site, DOI PEARL
  • Van Roessel P, Hayward NM, Barros CS & Brand AH 2002 'Two-color GFP imaging demonstrates cell-autonomy of GAL4-driven RNA interference indrosophila' genesis 34, (1-2) 170-173, DOI PEARL
John Bull Building

Contact Claudia Barros Lab – Neural Stem Cells and Brain Tumourigenesis Research

University of Plymouth, Peninsula School of Medicine The John Bull Building, Plymouth Science Park, 16 Research Way, Plymouth PL6 8BU UK