作者
Filipa Esteves,David V.C. Brito,Ana Teresa Rajado,Nádia Silva,Joana Apolónio,Vânia Palma Roberto,Inês M. Araújo,Clévio Nóbrega,Pedro Castelo‐Branco,José Bragança,Raquel P. Andrade,Sofia M. Calado,Maria Leonor Faleiro,Carlos A. Matos,Nuno Marques,Ana Marreiros,Hipólito Nzwalo,Sandra Pais,Isabel Palmeirim,Sónia Simão,Natércia Joaquim,Rui Miranda,António Pêgas,D. Raposo,Ana Paula Sardo
摘要
The unprecedented rise in life expectancy observed in the last decades is leading to a global increase in the ageing population, and age-associated diseases became an increasing societal, economic, and medical burden. This has boosted major efforts in the scientific and medical research communities to develop and improve therapies to delay ageing and age-associated functional decline and diseases, and to expand health span. The establishment of induced pluripotent stem cells (iPSCs) by reprogramming human somatic cells has revolutionised the modelling and understanding of human diseases. iPSCs have a major advantage relative to other human pluripotent stem cells as their obtention does not require the destruction of embryos like embryonic stem cells do, and do not have a limited proliferation or differentiation potential as adult stem cells. Besides, iPSCs can be generated from somatic cells from healthy individuals or patients, which makes iPSC technology a promising approach to model and decipher the mechanisms underlying the ageing process and age-associated diseases, study drug effects, and develop new therapeutic approaches. This review discusses the advances made in the last decade using iPSC technology to study the most common age-associated diseases, including age-related macular degeneration (AMD), neurodegenerative and cardiovascular diseases, brain stroke, cancer, diabetes, and osteoarthritis.