UCL  IRIS
Institutional Research Information Service
UCL Logo
Please report any queries concerning the funding data shown on the profile page to:

http://www.ucl.ac.uk/finance/secure/research/post_award
Please report any queries concerning the student data shown on the profile page to:

Email: portico-services@ucl.ac.uk

Help Desk: http://www.ucl.ac.uk/ras/portico/helpdesk
 More search options
Prof Sebastian Brandner
103
Institute of Neurology , UCL
Queen Square House
London
WC1N 3BG
Appointment
  • Professor of Neuropathology
  • Neurodegenerative Diseases
  • Institute of Neurology
  • Faculty of Brain Sciences
Biography

I started my research career during Medical School in Göttingen, at the Max Planck Institute of Biophysical Chemistry with Professor Creutzfeldt, where I studied the projection of the thalamocortical auditory system in the cat, resulting in several research publications as first author. 

During my postgraduate training in Neuropathology, I joined the Institute of Neuropathology in Zurich, where I started my research on prion disease, resulting in seminal publications in Nature and PNAS. 

After qualifying as a Consultant Neuropathologist in 1998, I established my own research group and developed mouse models to study neural development and brain tumours. In 2001, I was recruited through the MRC international recruitment scheme to join the MRC Prion Unit at UCL Institute of Neurology. 

In 2004 I was appointed as Chair of Neuropathology and Head of the Division of Neuropathology at Queen Square, one of the largest academic neuropathology departments in the UK.

At the MRC Prion Unit and the Institute of Neurology I integrated clinical neuropathology with experimental models on neurodegenerative diseases including prion diseases, which still remain a strong focus in my highly collaborative research. I am an expert on the pathology of both human and experimental models of prion disease worldwide and I maintains a close collaboration with the MRC Prion Unit and the National Prion Clinic at the National Hospital, Queen Square. 

I recently conducted a study “prevalence screening for the presence of vCJD prions” for the HPA, which has major implications for UK policy. At the Institute of Neurology, I also expanded my research on brain tumours which resulted in a number of excellent publications in Development and EMBO Journal. I developed a strong team working on brain cancer, and established close collaborations between UCL Cancer Centre and the Brain Tumour Unit at the National Hospital. I contribute nationally to brain cancer research in my role as council member of the British Neuro-oncology Society. Academic pathology and research on experimental models and their translation to human diseases are recognised key development areas in the UK. 











Research Summary

Modelling intrinsic brain tumours: Oncogenic signalling in neural stem cells

Intrinsic benign and malignant brain tumours, such as astrocytomas and glioblastoma are thought to originate from a population of stem cells in the adult brain. Stem cells divide in the adult brain to form more mature cells such as nerve cells (neurones) astrocytes (supporting cells) or oligodendrocytes (myelin forming cells that wrap processes of neurones in the white matter). We are working on the mechanisms of how mutations in genes that control cell division and migration of stem cells can cause brain tumours.

A novel aspect of our work is that the type of tumours depends on the pattern of mutations in stem cells, even when mutated stem cells are taken away from their normal environment and are placed in other areas of the brain. Knowledge of this mechanism is an important step towards the understanding where brain tumours originate from and how a certain type of brain tumour forms. 

How does the model work?

We inactivate tumour suppressor genes (PTEN, RB, p53) in the neural stem cell compartment. By injecting Cre-expressing virus into the ventricles of conditional knockout mice (PTENlox/lox, p53lox/lox and Rblox/lox in various combinations) the targeted genes are recombined only in cells located near the sub-ventricular zone (SVZ) which contains the largest known population of neural stem cells. In mice where Rb and p53, or the trio of the genes, PTEN, P53 and Rb are recombined, after several months, tumours of a specific phenotype resembling that of a human PNET develop. Instead, a tumour resembling human glioma (similar to oligoastrocytomas) is induced in mice where PTEN and P53 are targeted

Several weeks to months prior to the development of large tumours, small neoplastic lesions can be observed which we call microneoplasia. The assumption is that during the considerable time it takes to develop evident tumours additional genetic lesions are accumulated on top of the ones induced by Cre-recombination 







Teaching Summary

I actively contribute to capacity building in my role as educational supervisor for neuropathology trainees. I am advisor for training programmes at the London Deanery and contribute to training schemes in neuropathology. As chair of the academic group in the British Neuropathology Society (BNS) I organised a stimulating summer school (2009 & 2011) to bring together clinical scientists, neuropathology and neurology trainees.

I am Module Editor for the Module Neuro-Oncology in the DOH e-Learning for health
programme, an on-line resource of healthcare professionals which is now successfully completed.

Taught Courses: 

  • MSc students (2 Neuroscience and 1 Neuroradiology 

    modules)
  • Medical students 2nd and 3rd year:
  • Clinical Neuropathology
  • Clinical pathological conferences, seminars, courses.
  • Invited lectures in several UK Universities
  • Editorial team Queen Square Text book
  • Committee member North Thames Deanery Histopathology, STA, UCL College representative 



Excellent feedback results from students: 
  • Excellent feedback from UCL MSc courses (scores 4&5 of 5 in survey)

 Feedback from my lectures (UCL) reads as follows (e.g in 2010): “Prof 

Brandner’s lectures were the highlight of this pathology week.  They were 

engaging and interesting, balancing facts with background information, and his 

PowerPoint presentation was superbly structured and easy to follow with clear diagrams and excellent explanations of all that he had included.  The poster sessions were a good way of consolidating knowledge and Prof Brandner was extremely approachable to answer questions 



Appointments
04-OCT-2004 – 03-OCT-2021 Professor of Neuropathology Division of Neuropathology UCL Institute of Neurology, United Kingdom
01-DEC-2001 – 03-OCT-2004 Senior Neuropathologist MRC Prion Unit UCL Institute of Neurology, United Kingdom
01-JAN-1998 – 30-NOV-2001 Consultant Neuropathologist Neuropathology University Hospital Zurich, Switzerland
Academic Background
1991 Priv-Doz Privatdozent Georg-August-Universität Göttingen
1989 MD Doctor of Medicine Georg-August-Universität Göttingen
Please report any queries concerning the data shown on this page to:

https://www.ucl.ac.uk/hr/helpdesk/helpdesk_web_form.php
University College London - Gower Street - London - WC1E 6BT Tel:+44 (0)20 7679 2000

© UCL 1999–2011

Search by