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Simona Chera

Associate Professor, NCMM Young Associate Investigator
  • E-mailSimona.Chera@uib.no
  • Phone+47 55 97 12 62
  • Visitor Address
    Barne- og ungdomssjukehuset (BUS1)
    Haukelandsbakken 15
    5021 Bergen
    Room 
    6110, 6th floor
  • Postal Address
    Postboks 7804
    5020 Bergen

Simona Chera obtained her PhD from Department of Genetics and Evolution, at the Faculty of Science, University of Geneva, in 2008, with a focus on cellular and molecular mechanisms acting in regeneration. Afterwards, she was a postdoctoral fellow in Prof. Pedro Herrera lab, characterizing the two age-dependent regenerative mechanisms involved in spontaneous murine pancreatic β-cell regeneration (Thorel et al. 2010, Nature and Chera et al. 2014, Nature). In March 2015, she moved to Bergen, as a postdoctoral fellow in Ræder lab, working on a project involving the differentiation of pancreatic β-cells from human induced pluripotent stem cells, derived from fibroblasts donated by patients with Mature Onset Diabetes of the Young (MODY). She is now an Associate Professor at the Department of Clinical Science, University of Bergen and NCMM Young Associate Investigator. 

The main focus throughout her career has been the characterization of the cellular processes and molecular cues governing the balance between tissue regeneration and homeostasis. This has resulted in numerous publications.

Recently, she received several prestigious grants: the Novo Nordisk Foundation Excellence Project for Endocrinology Research, for characterizing and reversing β-cell senescence and proliferation quiescence in monogenic diabetes; and Young Talent Research Projects funded by the Research Council of Norway, aiming at characterizing the cellular and molecular basis of the gradual failure of insulin-producing β-cells in diabetes by using a novel in vivo strategy involving transplanted induced pluripotent stem cells (iPSCs) derived from monogenic diabetes patients (MODY patients).

Selected publications:

  1. Legøy TA*, Vethe H*, Abadpour S, Strand BL, Scholz H, Paulo JA, Ræder H, Ghila LChera S. Encapsulation boosts islet-cell signature in differentiating human induced pluripotent stem cells via integrin signaling. Scientific Reports 2020 Jan 15;10(1):414. doi: 10.1038/s41598-019-57305-x [BioRxiv 2019 Oct 04, preprint doi: 10.1101/791442]
  2. Legøy TA, Mathisen AF, Salim Z, Vethe H, Bjørlykke Y, Abadpour S, Paulo JA, Scholz H, Raeder H, Ghila L, Chera S. In vivo Environment Swiftly Restricts Human Pancreatic Progenitors Toward Mono-Hormonal Identity via a HNF1A/HNF4A Mechanism. Frontiers in Cell and Developmental Biology 2020 Feb 25;8:109. eCollection 2020. doi: 10.3389/fcell.2020.00109
  3. Legøy TA, Ghila L, Vethe H, Abadpour S, Mathisen AF, Paulo JA, Scholz H, Raeder H, Chera S. In vivo hyperglycemia exposure elicits distinct period-dependent effects on human pancreatic progenitor differentiation, conveyed by oxidative stress. Acta Physiologica (Oxf) 2020 Apr;228(4):e13433. Epub 2020 Jan 8. doi: 10.1111/apha.13433. PMID:31872528
Selected publications
  • Cigliola, Valentina; Ghila, Luiza; Chera, Simona; Herrera, Pedro L. 2019. Tissue repair brakes: A common paradigm in the biology of regeneration: Concise review. Stem Cells. doi: 10.1002/stem.3118
  • Furuyama, Kenichiro; Chera, Simona; van Gurp, Leon; Oropeza, Daniel; Ghila, Luiza; Damond, Nicolas; Vethe, Heidrun; Paulo, Joao A.; Joosten, Antoinette M.; Berney, Thierry; Bosco, Domenico; Dorrell, Craig; Grompe, Markus; Ræder, Helge; Roep, Bart O.; Thorel, Fabrizio; Herrera, Pedro L. 2019. Diabetes relief in mice by glucose-sensing insulin-secreting human α-cells. Nature. 567: 43-48. doi: 10.1038/s41586-019-0942-8
  • Cigliola, Valentina; Ghila, Luiza; Thorel, Fabrizio; van Gurp, Leon; Baronnier, Delphine; Oropeza, Daniel; Gupta, Simone; Miyatsuka, Takeshi; Kaneto, Hideaki; Magnuson, Mark A; Osipovich, Anna B; Sander, Maike; Wright, Christopher EV; Thomas, Melissa K; Furuyama, Kenichiro; Chera, Simona; Herrera, Pedro L. 2018. Pancreatic islet-autonomous insulin and smoothened-mediated signalling modulate identity changes of glucagon+ α-cells. Nature Cell Biology. 20: 1267-1277. doi: 10.1038/s41556-018-0216-y
  • Chera, Simona; Herrera, Pedro L. 2016. Regeneration of pancreatic insulin-producing cells by in situ adaptive cell conversion. Current Opinion in Genetics and Development. 40: 1-10. doi: 10.1016/j.gde.2016.05.010

Methods in Medical Cell Biology - BMED320 ECTS credits: 25

Future medicine - ELMED303 ECTS credits: 3

Academic article
  • 2020. In vivo hyperglycaemia exposure elicits distinct period-dependent effects on human pancreatic progenitor differentiation, conveyed by oxidative stress. Acta Physiologica. 1-16.
  • 2019. The effect of WnT pathway modulators on human iPSC-derived pancreatic beta cell maturation. Frontiers in Endocrinology. 1-13.
  • 2019. Reprogrammed cells display distinct proteomic signaturesAssociated with colony morphology variability. Stem Cells International. 1-16.
  • 2019. In vivo hyperglycemia exposure elicits distinct period-dependent effects on human pancreatic progenitor differentiation, conveyed by oxidative stress. Acta Physiologica. 1-16.
  • 2019. Diabetes relief in mice by glucose-sensing insulin-secreting human α-cells. Nature. 43-48.
  • 2018. Pancreatic islet-autonomous insulin and smoothened-mediated signalling modulate identity changes of glucagon+ α-cells. Nature Cell Biology. 1267-1277.
  • 2018. Novel protein signatures suggest progression to muscular invasiveness in bladder cancer. PLOS ONE. 1-15.
  • 2017. Probing the missing mature β-cell proteomic landscape in differentiating patient iPSC-derived cells. Scientific Reports. 1-14.
  • 2017. Converting adult pancreatic islet α cells into β cells by targeting both Dnmt1 and Arx. Cell Metabolism. 622-634.
Popular scientific article
  • 2019. Encapsulation boosts islet-cell signature in differentiating human induced pluripotent stem cells via integrin signalling. bioRxiv - the preprint server for biology.
Academic literature review
  • 2019. Tissue repair brakes: A common paradigm in the biology of regeneration: Concise review.
  • 2016. Stress-induced adaptive islet cell identity changes. 87-96.
  • 2016. Regeneration of pancreatic insulin-producing cells by in situ adaptive cell conversion. 1-10.

More information in national current research information system (CRIStin)