Robert Passier

ORCID: 0000-0003-4312-9296
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About
Contact & Profiles
Research Areas
  • Pluripotent Stem Cells Research
  • 3D Printing in Biomedical Research
  • Tissue Engineering and Regenerative Medicine
  • Congenital heart defects research
  • CRISPR and Genetic Engineering
  • Neuroscience and Neural Engineering
  • Cardiomyopathy and Myosin Studies
  • Cardiac electrophysiology and arrhythmias
  • Electrospun Nanofibers in Biomedical Applications
  • Medical Imaging Techniques and Applications
  • RNA Research and Splicing
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Medical and Biological Sciences
  • Immunotherapy and Immune Responses
  • Cell Adhesion Molecules Research
  • RNA modifications and cancer
  • Microfluidic and Capillary Electrophoresis Applications
  • Microfluidic and Bio-sensing Technologies
  • Genomics and Chromatin Dynamics
  • RNA and protein synthesis mechanisms
  • Renal and related cancers
  • Mesenchymal stem cell research
  • Cellular Mechanics and Interactions
  • Virus-based gene therapy research
  • Ion channel regulation and function

University of Twente
2016-2025

Leiden University
2013-2025

Leiden University Medical Center
2011-2023

Stem Cell Technology (Taiwan)
2016-2020

Royal Netherlands Academy of Arts and Sciences
2017

University of Glasgow
2017

Amsterdam UMC Location University of Amsterdam
2011

Newcastle University
2011

Hubrecht Institute for Developmental Biology and Stem Cell Research
2002-2010

Utrecht University
2007-2010

Background— Cardiomyocytes derived from human embryonic stem (hES) cells could be useful in restoring heart function after myocardial infarction or failure. Here, we induced cardiomyocyte differentiation of hES by a novel method and compared their electrophysiological properties coupling with those primary fetal cardiomyocytes. Methods Results— were cocultured visceral-endoderm (VE)–like the mouse. This initiated to beating muscle. Sarcomeric marker proteins, chronotropic responses, ion...

10.1161/01.cir.0000068356.38592.68 article EN Circulation 2003-05-13
Peter Arner Carsten O. Daub Kristoffer Vitting‐Seerup Robin Andersson Berit Lilje and 95 more Finn Drabløs Andreas Lennartsson Michelle Rönnerblad Olga Hrydziuszko Morana Vitezic Tom C. Freeman Ahmad M. N. Alhendi Peter Arner Richard A Axton J. Kenneth Baillie Anthony G Beckhouse Beatrice Bodega James Briggs Frank Brombacher Margaret R. Davis Michael Detmar Anna Ehrlund Mitsuhiro Endoh Afsaneh Eslami Michela Fagiolini Lynsey Fairbairn Geoffrey J. Faulkner Carmelo Ferrai Malcolm E Fisher Lesley M. Forrester Dan Goldowitz Reto Guler Thomas J Ha Mitsuko Hara Meenhard Herlyn Tomokatsu Ikawa Chieko Kai Hiroshi Kawamoto Levon M. Khachigian S. Peter Klinken Soichi Kojima Haruhiko Koseki Sarah Klein Niklas Mejhert Ken Miyaguchi Yosuke Mizuno Mitsuru Morimoto Kelly J Morris Christine L. Mummery Yutaka Nakachi Soichi Ogishima Mariko Okada Yasushi Okazaki Valerio Orlando Dmitry A. Ovchinnikov Robert Passier Margaret Patrikakis Ana Pombo Xian‐Yang Qin Sugata Roy Hiroki Sato Suzana Savvi Alka Saxena Anita Schwegmann Daisuke Sugiyama Rolf Swoboda Hiroshi Tanaka Andru Tomoiu Louise N Winteringham Ernst J. Wolvetang Chiyo Yanagi-Mizuochi Misako Yoneda Susan E. Zabierowski Peter Zhang Imad Abugessaisa Nicolas Bertin Alexander D. Diehl Shiro Fukuda Masaaki Furuno Jayson Harshbarger Akira Hasegawa Fumi Hori Sachi Ishikawa-Kato Yuri Ishizu Masayoshi Itoh Tsugumi Kawashima Miki Kojima Naoto Kondo Marina Lizio Terrence F. Meehan Chris Mungall Mitsuyoshi Murata Hiromi Nishiyori-Sueki Serkan Sahin Sayaka Nagao-Sato Jessica Severin Michiel de Hoon Jun Kawai Takeya Kasukawa Timo Lassmann

Although it is generally accepted that cellular differentiation requires changes to transcriptional networks, dynamic regulation of promoters and enhancers at specific sets genes has not been previously studied en masse. Exploiting the fact active are transcribed, we simultaneously measured their activity in 19 human 14 mouse time courses covering a wide range cell types biological stimuli. Enhancer RNAs, then messenger RNAs encoding transcription factors, dominated earliest responses....

10.1126/science.1259418 article EN Science 2015-02-13

Defined growth conditions are essential for many applications of human embryonic stem cells (hESC). Most defined media presently used in combination with Matrigel, a partially extracellular matrix (ECM) extract from mouse sarcoma. Here, we ECM requirements hESC by analyzing integrin expression and production determined function using blocking antibodies. expressed all major proteins corresponding integrins. We then systematically replaced Matrigel medium supplements proteins. Cells attached...

10.1634/stemcells.2008-0291 article EN Stem Cells 2008-07-03

Maximizing baseline function of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) is essential for their effective application in models cardiac toxicity and disease. Here, we aimed to identify factors that would promote an adequate level permit robust single-cell contractility measurements a induced cell (hiPSC) model hypertrophic cardiomyopathy (HCM). A simple screen revealed the collaborative effects thyroid hormone, IGF-1 glucocorticoid analog dexamethasone on...

10.1016/j.celrep.2015.09.025 article EN cc-by Cell Reports 2015-10-01

Human embryonic stem cells (hESCs) can differentiate into cardiomyocytes, but the efficiency of this process is low. We routinely induce cardiomyocyte differentiation HES‐2 cell line by coculture with a visceral endoderm‐like line, END‐2, in presence 20% fetal calf serum (FCS). In study, we demonstrate striking inverse relationship between and concentration FCS during HES‐2‐END‐2 coculture. The number beating areas cocultures was increased 24‐fold absence compared FCS. An additional 40%...

10.1634/stemcells.2004-0184 article EN Stem Cells 2005-05-25

Calmodulin kinase (CaMK) II is linked to arrhythmia mechanisms in cellular models where repolarization prolonged. CaMKII upregulation and prolonged are general features of cardiomyopathy, but the role arrhythmias cardiomyopathy unknown.We studied a mouse model cardiac hypertrophy attributable transgenic (TG) overexpression constitutively active form CaMKIV that also has increased endogenous activity. ECG-telemetered TG mice had significantly more than wild-type (WT) littermate controls at...

10.1161/01.cir.0000027583.73268.e7 article EN Circulation 2002-09-03

Cell transplantation may restore heart function in disease associated with loss or dysfunction of cardiomyocytes. Recently, Laflamme et al reported an improvement cardiac immunodeficient rats 4 weeks after coronary artery ligation and injection human embryonic stem cell-derived cardiomyocytes (hESC-CMs). We have recently carried out a comparable study transplanting hESC-CMs to the hearts mice myocardial infarction. Our findings were similar up 4-week time point, significant improvements...

10.1161/circresaha.108.175505 article EN Circulation Research 2008-04-25

Mammals are unable to regenerate their heart after major cardiomyocyte loss caused by myocardial infarction. Human embryonic stem cells (hESCs) can give rise functional cardiomyocytes and therefore have exciting potential as a source of for replacement therapy. Understanding the molecular regulation differentiation from is crucial stepwise enhancement scaling production that will be necessary transplantation Our novel hESC protocol now efficient enough meaningful genome-wide transcriptional...

10.1634/stemcells.2006-0054 article EN Stem Cells 2006-05-05

Differentiated derivatives of human pluripotent stem cells (hPSCs) are often considered immature because they resemble foetal more than adult, with hPSC-derived cardiomyocytes (hPSC-CMs) being no exception. Many functional features these CMs, such as their cell morphology, electrophysiological characteristics, sarcomere organization and contraction force, underdeveloped compared to adult cardiomyocytes. However relatively little is known on how gene expression profiles compare the heart, in...

10.1242/dev.123810 article EN Development 2015-01-01
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