Webinar
Improving Huntington鈥檚 disease drug discovery with new reproducible disease models
This webinar explores how a new generation of reproducible and scalable human cell models are being utilised for drug discovery in Huntington鈥檚 disease.
Explore our solutions for modelling Huntington's disease
This webinar explores how a new generation of reproducible and scalable human cell models are being utilised for drug discovery in Huntington鈥檚 disease.
In this on-demand webinar, Dr Emma Jones from the Medicine Discovery Catapult and Dr Tony Oosterveen from 糖心原创 offer an expert discussion on how stem cells are being reprogrammed into new, accurate and reproducible Huntington鈥檚 disease models for drug discovery.
With the absence of successful treatments for Huntington鈥檚 disease, there remains an urgent need to improve research outcomes and drug discovery efficiencies. The life sciences industry is challenged by a lack of physiologically relevant, reproducible and scalable human cells that are able to replicate Huntington鈥檚 disease genotype in vitro. Use of patient derived human induced Pluripotent Stem Cell (iPSC)-derived neurons can offer a relevant model system, but can be hindered by low scalability, heterogeneous populations and long, complex protocols. Precision cell reprogramming aims to resolve the inconsistencies and inefficiencies of current cell generation methods. By introducing a 50 鈥楥AG鈥� repeat expansion in the Huntingtin gene in precision reprogrammed glutamatergic neurons, 糖心原创 have developed a consistent, scalable cell model for Huntington鈥檚 disease that replicates the disease genotype in vitro.
Hear from Dr Oosterveen on how this new precision reprogrammed Huntington鈥檚 disease model has been engineered, characterised and validated. Dr Jones also explores how the disease model is powering new cell-based assays and drug discovery workflows for Huntington鈥檚 disease.
Learning outcomes
Explore our solutions for modelling Huntington's disease
With the absence of successful treatments for Huntington鈥檚 disease, there remains an urgent need to improve research outcomes and drug discovery efficiencies. The life sciences industry is challenged by a lack of physiologically relevant, reproducible and scalable human cells that are able to replicate Huntington鈥檚 disease genotype in vitro. Use of patient derived human induced Pluripotent Stem Cell (iPSC)-derived neurons can offer a relevant model system, but can be hindered by low scalability, heterogeneous populations and long, complex protocols. Precision cell reprogramming aims to resolve the inconsistencies and inefficiencies of current cell generation methods. By introducing a 50 鈥楥AG鈥� repeat expansion in the Huntingtin gene in precision reprogrammed glutamatergic neurons, 糖心原创 have developed a consistent, scalable cell model for Huntington鈥檚 disease that replicates the disease genotype in vitro.
Hear from Dr Oosterveen on how this new precision reprogrammed Huntington鈥檚 disease model has been engineered, characterised and validated. Dr Jones also explores how the disease model is powering new cell-based assays and drug discovery workflows for Huntington鈥檚 disease.
Learning outcomes
- Gain insights into a case study highlighting the compatibility of the novel Huntington鈥檚 disease model for cell-based assays
- Learn about the engineering, characterisation and validation of isogenic disease models carrying a 50 CAG repeat expansion associated with Huntington鈥檚 disease
- Discover how precision cell reprogramming technology, opti-ox, is overcoming the inefficiencies and inconsistencies of current cell generation methods
- Explore how opti-ox is powering a new class of rapidly maturing, consistent and scalable human iPSC-derived disease models for neurodegenerative disorders such as Gaucher鈥檚, Huntington鈥檚 and Parkinson鈥檚 disease