Leverhulme Grant Awarded!

The Bianco Lab had a lot to celebrate this week. Not only was Asaph’s paper accepted, but UCL was awarded a Leverhulme Grant to support a project in the lab linking dynamic brain activity to flexible behaviour.

A celebratory dinner was very much in order!

Recurrent networks shape response variability

Recurrent networks shape response variability

In a recent paper from the Bianco Lab, we used light-sheet calcium imaging and computational modelling to explore how activity in neural networks affects their internal state and contributes to variability in activity and behaviour.

One of our key findings is that recurrent network interactions can explain multiple aspects of tectal physiology including the structure of spontaneous activity, variability in visual encoding, and habituation of prey-catching behaviour.

Congratulations to first author Asaph Zylbertal, and check out the paper here: https://elifesciences.org/articles/78381

Zeeks - Art for Geeks by Dr. Elisabeth Kugler

We are excited to share that our previous postdoc Dr. Elisabeth Kugler started her own company “Zeeks - Art for Geeks” where she combines her passion for science and art. She offers consulting on data analysis and offers beautiful high resolution images of the zebrafish retina and vasculature as science art and merchandise.

Go check it out https://zeeks-artforgeeks.com.

MacDonald lab has a new lab technician

We would like to welcome our new lab technician Aanandita Kothurkar who has joined us since January from Karin Tuschl’s lab where she did a masters titled “Elucidating the role of ATP13A1 in manganese transport and neurodevelopment”.

Our GliaMorph paper has been accepted for publication in Development

We are excited to announce that our paper “GliaMorph: A modular image analysis toolkit to quantify Müller glial cell morphology” will be published in Development. The paper has been made in collaboration with Elisabeth Kugler, Isabel Bravo, Xhuljana Durmishi, Stefania Marcotti, Sara Beqiri, Alicia Carrington, Brian M. Stramer, Pierre Mattar and Ryan B. MacDonald.

https://journals.biologists.com/dev/article/doi/10.1242/dev.201008/286420/GliaMorph-A-modular-image-analysis-toolkit-to

Welcoming another Master's student, Lidia

We are excited to welcome another Master’s student, Lidia, to the lab. She will be working on ascertaining the localisation and function of mitochondria during development of Müller glial cells in the retina, and whether this impacts retinal activity.

Our new master's student Yaoyang

We would like to welcome our new Master’s student Yaoyang to the lab. His project will be investigating the joint role of microglia and Müller glia in the phagocytosis of dying cells in the zebrafish retina and the related mechanisms.

MacDonald and Chu lab's Christmas party 2022

The MacDonald-Chu laboratories came together to celebrate the end of 2022. It was a fun day of bowling and dinner in Finsbury Park. We're looking forward to the groups continuing to grow with young scientists and many more social occasions in 2023. 

The Wilson Lab are looking for a Research Technician

The Wilson Lab are looking for a Research Technician

We are excited to announce that we are looking for an enthusiastic research technician to join our team embarking on a new project.

The successful candidate will have the exciting opportunity to train and work closely with a senior postdoctoral fellow (Chintan Trivedi) on cutting edge techniques such as CRISPRR-Cas9, single cell transcriptomics, high throughput screening and multiplexed in situ hybridisation approaches as well as behaviour analysis.

The position is funded by a Wellcome Trust Discovery Award for 2 years in the first instance at Grade 6, currently £31,131 - £36,348. The position could start as soon as possible, we are envisioning the successful candidate to start by 1. February 2023.

The link to the application on UCL.ac.uk/jobs is via the button below. The current closing date is 2 December 2022.

Please email Anukampa Barth a.barth@ucl.ac.uk of further information.


 

Luciana Moreira visits the Wilson lab

Luciana Moreira visits the Wilson lab

Luciana Moreira visited the Wilson lab this October, along with her colleague Francisca Coutinho. At the Alves lab in the Instituto Nacional de Saúde Dr. Ricardo Jorge (INSA), Porto, they study the lysosomal storage disease mucopolysaccharidosis. The lab has recently decided to begin using zebrafish (with no prior experience!) to model these diseases and approached the Wilson lab for help. Luciana and Francisca were given training by Hande and Stephen in generating CRISPR F0s (along with lots of general fish advice), with help from Francois, Declan, Elena and many other members of the fish floor. We had a great time hosting Luciana and Francisca and welcome them to the zebrafish community!

Welcome Eleni!

The Bianco lab welcomes their newest postdoc, Eleni Petridou!

WELCOME MATTHIAS!

Welcome to Matthias who joins the Bianco lab from the Wellcome Optical Biology PhD programme.

First person – Karin Tuschl

First person – Karin Tuschl

First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Karin Tuschl is first author on ‘ Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish’, published in DMM.

Read the interview with Karin about her work investigating the role of manganese in brain physiology and disease.

First Person-Karin Tuschl

Dis Model Mech (2022) 15 (6): dmm049641.

https://doi.org/10.1242/dmm.049641

Zebrafish help us understand a disabling childhood disorder of manganese transport

Zebrafish help us understand a disabling childhood disorder of manganese transport

“Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish”

Full paper in Disease Models and Mechanisms: https://journals.biologists.com/dmm/article/doi/10.1242/dmm.044594/275312/

Zebrafish brain showing changes in neuronal activity upon manganese neurotoxicity: diminished activity in green, increased activity in magenta, scale bar 100µm (Credit to Chintan Trivedi).

Dysregulation of the metal manganese in the brain underlies movement abnormalities in a rare inherited disorder of manganese transport leading to disability in early childhood.

Manganese is an essential trace metal present in our diet that is required for normal brain function. However, excess manganese is toxic to the brain, particularly to regions required for movement control. Therefore, it is crucial that the body tightly regulates manganese levels.

Dr Tuschl in collaboration with other UCL groups has recently identified an inherited disorder caused by abnormalities in the gene SLC39A14 that is required for manganese transport across the cell. Impaired control of the body's manganese load results in manganese accumulation in the brain. Affected children suffer from a disabling movement disorder and often become wheelchair bound within the first years of life. Current treatment options are limited and burdensome. Therefore, there is a real need to better understand the disease mechanisms in order to identify new treatment targets and strategies. 

Using a zebrafish model of this manganese transport disorder this study has identified how manganese regulation is impaired in the brain leading to both toxic effects of manganese as well as manganese deficiency. Subsequently, this impacts on the regulation of calcium that is required for normal neuronal function. These changes are associated with impaired neuronal activity in the brain of zebrafish and reduced swimming behaviour.

https://www.ucl.ac.uk/child-health/news/2022/jun/zebrafish-help-us-understand-disabling-childhood-disorder

A Structural Atlas of the Developing Zebrafish Telencephalon

A Structural Atlas of the Developing Zebrafish Telencephalon

The Wilson Lab in collaboration with Monica Folgueira from the University of A Coruña have published a paper focussed on the development of the telencephalon. We had a lot of help from some other Wilson Lab alumni: Pedro, Leo Valdivia and Isaac Bianco.

This paper forms part of a Research topic for the journal Frontiers in Neuroanatomy: Teleostean Forebrain Organization and Evolution: Links to Behaviour and Ecological Niche

How do bilaterally equivalent structures in the forebrain become left-right asymmetric?

How do bilaterally equivalent structures in the forebrain become left-right asymmetric?

New insights into brain asymmetry and a novel Wnt pathway protein!

Check out our preprint on biorxiv

Cachd1 is a novel Frizzled- and LRP6-interacting protein required for neurons to acquire left-right asymmetric character

Cachd1 is a novel Wnt pathway component that bridges FZD and LRP6 co-receptors. Asymmetric modulation of Wnt signalling by Cachd1 leads to lateralisation of Hb neurons by altering timing of neurogenesis and probabalistic selection between lateralised neuronal fates.

This was a fantastic collaborative effort between the Wilson Lab and the Yvonne Jones, Raible and Li Labs and Gavin J Wright. With four joint lead authors; Gareth Powell, Yuguang Zhao, Ana Faro & Heather Stickney.

Read a lay summary of this publication here!



Postdoc position in Bianco Lab

Postdoc position in Bianco Lab

The Bianco lab is looking for postdocs to join a Wellcome funded project examining how circuits integrate sensory and internal state information to select behavioural programmes and how sequences of motor actions are flexibly selected and tuned to accomplish behavioural goals. The lab uses a variety of approaches including functional calcium imaging, naturalistic behavioural assays, multiphoton optogenetics, circuit tracing and computational modelling.

Please contact Isaac to find out more and apply before 6 June 2022: bit.ly/3M1rwsT