The use of induced pluripotent stem cell-derived vascular smooth muscle cells to study aneurysmal diseases
Scope of the method
- Human health
- Basic Research
- Translational - Applied Research
- In vitro - Ex vivo
- Human derived cells / tissues / organs
Description
- induced pluripotent stem cells
- drug screening
- Disease modeling
- Lateral mesoderm
- Neural crest
- thoracic aortic aneurysm
- Marfan syndrome
- Loeys-Dietz syndrome
Vascular smooth muscle cell (VSMC) deficiency plays a pivotal role in aneurysm development. Unfortunately, access to native VSMCs of patients and (particularly) control individuals is extremely limited. It has been shown that iPSC-derived VSMCs recapitulate the yet known disease processes very well. They can thus serve as a substitute for their native counterparts when studying and therapeutically targeting human aneurysmal phenotypes. Even the fact that tissue VSMCs of different embryonic origins discretely contribute to disease development and/or progression can be accounted for by using specific differentiation protocols for mesoderm- and neural crest-derived VSMCs. In our research team we use iPSC-VSMCs to assist the search for modifier genes, to further unravel the disease mechanisms and to find novel drug compounds.
- Still in development
- Internally validated
Contact person
Aline VerstraetenOrganisations
University of Antwerp (UAntwerpen)Center for Medical Genetics
Belgium
Flemish Region