Maria Margarida Diogo

Dr. Maria Margarida Diogo

Department of Bioengineering and iBB - Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Lisboa 1049-001, Portugal
orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2009 in Trends in Biotechnology
Verified
Journal Article
Closed access
Tiago FernandesTiago Fernandes
Tiago Fernandes
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
DCDouglas S. Clark
Douglas S. Clark
JDJonathan Dordick
Jonathan Dordick
Joaquim M.S. CabralJoaquim M.S. Cabral
Joaquim M.S. Cabral

1 November 2011 in Biotechnology Advances
Verified
Journal Article
Closed access
CRCarlos A.V. Rodrigues
Carlos A.V. Rodrigues
Tiago FernandesTiago Fernandes
Tiago Fernandes
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
CSCláudia Lobato da Silva
Cláudia Lobato da Silva
Joaquim M.S. CabralJoaquim M.S. Cabral
Joaquim M.S. Cabral

1 March 2005 in Journal of Chromatography A
Verified
Journal Article
Closed access
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
JQJ.A. Queiroz
J.A. Queiroz
Duarte Miguel PrazeresDuarte Miguel Prazeres
Duarte Miguel Prazeres

1 October 2007 in Journal of Biotechnology
Verified
Journal Article
Closed access
AFAna Fernandes-Platzgummer
Ana Fernandes-Platzgummer
Tiago FernandesTiago Fernandes
Tiago Fernandes
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
CSC. Lobato da Silva
C. Lobato da Silva
DHD. Henrique
D. Henrique
Joaquim M.S. CabralJoaquim M.S. Cabral
Joaquim M.S. Cabral

25 June 2019 in Scientific Reports
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Journal Article
Open access
PDF file
MBMariana Branco
Mariana Branco
JCJoão Cotovio
João Cotovio
CRCarlos A.V. Rodrigues
Carlos A.V. Rodrigues
SVSandra H. Vaz
Sandra H. Vaz
Tiago FernandesTiago Fernandes
Tiago Fernandes
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
Human induced pluripotent stem cells (hiPSCs) represent an almost limitless source of cells for disease modelling and drug screening applications. Here we established an efficient and robust 3D platform for cardiomyocyte (CMs) production from hiPSCs, solely through small-molecule-based temporal modulation of the Wnt signalling, which generates more than 90% cTNT+ cells. The impact of performing the differentiation process in 3D conditions as compared to a 2D culture system, was characterized by transcriptomic analysis by using data collected from sequential stages of 2D and 3D culture. We highlight that performing an initial period of hiPSC aggregation before cardiac differentiation primed hiPSCs towards an earlier mesendoderm lineage differentiation, via TGF-β/Nodal signaling stabilization. Importantly, it was also found that CMs in the 3D microenvironment mature earlier and show an improved communication system, which we suggested to be responsible for a higher structural and functional maturation of 3D cardiac aggregates.

10 December 2020 in Frontiers in Cell and Developmental Biology
Verified
Journal Article
Open access
PDF file
AGAna Rita Gomes
Ana Rita Gomes
Tiago FernandesTiago Fernandes
Tiago Fernandes
SVSandra H. Vaz
Sandra H. Vaz
TSTeresa P. Silva
Teresa P. Silva
EBEvguenia P. Bekman
Evguenia P. Bekman
Maria Margarida DiogoMaria Margarida Diogo
Maria Margarida Diogo
Engineering brain organoids from human induced pluripotent stem cells (hiPSCs) is a powerful tool for modeling brain development and neurological disorders. Rett syndrome (RTT), a rare neurodevelopmental disorder, can greatly benefit from this technology, since it affects multiple neuronal subtypes in forebrain sub-regions. We have established dorsal and ventral forebrain organoids from control and RTT patient-specific hiPSCs recapitulating 3D organization and functional network complexity. Our data revealed a premature development of the deep-cortical layer, associated to the formation of TBR1 and CTIP2 neurons, and a lower expression of neural progenitor/proliferative cells in female RTT dorsal organoids. Moreover, calcium imaging and electrophysiology analysis demonstrated functional defects of RTT neurons. Additionally, assembly of RTT dorsal and ventral organoids revealed impairments of interneuron’s migration. Overall, our models provide a better understanding of RTT during early stages of neural development, demonstrating a great potential for personalized diagnosis and drug screening.