Michel Goedert

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Michel Goedert FRS, FMedSci is a Luxembourgish-British neuroscientist and former Head of Neurobiology, at the MRC Laboratory of Molecular Biology. [1]

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Goedert was born and raised in Luxembourg. After finishing his medical studies at the University of Basel in 1986, he started working at the Medical Research Council Laboratory of Molecular Biology affiliated with the University of Cambridge.

Goedert was awarded the Metlife Foundation Award for Medical Research in Alzheimer's Disease in 1996, the Potamkin Prize in 1998 and the European Grand Prix for Research by the Foundation for Research on Alzheimer's disease in 2014. In 2018 he was one of four recipients of the Grete Lundbeck European Brain Research Prize with the citation "For their groundbreaking research on the genetic and molecular basis of Alzheimer's disease, with far-reaching implications for the development of new therapeutic interventions as well as for the understanding of other neurodegenerative diseases of the brain". [2] In 2019 he received the Royal Medal. [3] and the Rainwater Charitable Foundation prize for outstanding innovation in neurodegenerative disorder research. [4]

He is married to Maria Grazia Spillantini, a geneticist with whom he has one son, Thomas.

Research

Goedert's work combines biochemical, molecular biological and structural techniques to investigate common neurodegenerative diseases, including Alzheimer's and Parkinson's. [5] His research focused on the abnormal filamentous inclusions that characterise Parkinson's and Alzheimer's, showing that the intracellular filaments of these diseases are made of either alpha-synuclein or tau protein. [6] Goedert's team identified mutations in MAPT, the tau gene, that cause rare inherited forms of frontotemporal dementia with tau inclusions, establishing a central role for tau assembly in the disease. [7]

Works

Related Research Articles

Lewy body Spherical inclusion commonly found in damaged neurons

Lewy bodies are the inclusion bodies – abnormal aggregations of protein – that develop inside nerve cells affected by Parkinson's disease (PD), the Lewy body dementias, and some other disorders. They are also seen in cases of multiple system atrophy, particularly the parkinsonian variant (MSA-P).

Tau protein Group of six protein isoforms produced from the MAPT gene

The tau proteins are a group of six highly soluble protein isoforms produced by alternative splicing from the gene MAPT. They have roles primarily in maintaining the stability of microtubules in axons and are abundant in the neurons of the central nervous system (CNS). They are less common elsewhere but are also expressed at very low levels in CNS astrocytes and oligodendrocytes.

Tauopathy Medical condition

Tauopathy belongs to a class of neurodegenerative diseases involving the aggregation of tau protein into neurofibrillary or gliofibrillary tangles in the human brain. Tangles are formed by hyperphosphorylation of the microtubule protein known as tau, causing the protein to dissociate from microtubules and form insoluble aggregates. The mechanism of tangle formation is not well understood, and whether tangles are a primary cause of Alzheimer's disease or play a peripheral role is unknown.

Neurodegenerative disease Central nervous system disease

A neurodegenerative disease is caused by the progressive loss of structure or function of neurons, in the process known as neurodegeneration. Such neuronal damage may ultimately involve cell death. Neurodegenerative diseases include amyotrophic lateral sclerosis, multiple sclerosis, Parkinson's disease, Alzheimer's disease, Huntington's disease, multiple system atrophy, and prion diseases. Neurodegeneration can be found in the brain at many different levels of neuronal circuitry, ranging from molecular to systemic. Because there is no known way to reverse the progressive degeneration of neurons, these diseases are considered to be incurable; however research has shown that the two major contributing factors to neurodegeneration are oxidative stress and inflammation. Biomedical research has revealed many similarities between these diseases at the subcellular level, including atypical protein assemblies and induced cell death. These similarities suggest that therapeutic advances against one neurodegenerative disease might ameliorate other diseases as well.

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References

  1. "Michel Goedert". Alzforum. 19 October 2008. Retrieved 20 December 2019.
  2. "The Brain Prize Winners 2018 - Lundbeckfonden - The Brain Prize". www.thebrainprize.org. Retrieved 20 December 2019.
  3. Royal Medal 2019
  4. The Rainwater Prize Program
  5. "Biography Michel Goedert - Lundbeckfonden - The Brain Prize". www.thebrainprize.org. Retrieved 20 December 2019.
  6. Avenue, Francis Crick. "Michel Goedert". MRC Laboratory of Molecular Biology. Retrieved 20 December 2019.
  7. Paul Brackley (24 March 2018). "Winner of Brain Prize 2018, Prof Michel Goedert, on our best hope for tackling Alzheimer's disease". Cambridge Independent. Retrieved 20 December 2019.