Charles E. Murry

ORCID: 0000-0003-3862-6773
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About
Contact & Profiles
Research Areas
  • Tissue Engineering and Regenerative Medicine
  • Pluripotent Stem Cells Research
  • Congenital heart defects research
  • Electrospun Nanofibers in Biomedical Applications
  • CRISPR and Genetic Engineering
  • 3D Printing in Biomedical Research
  • Cardiomyopathy and Myosin Studies
  • Cardiac Ischemia and Reperfusion
  • Muscle Physiology and Disorders
  • Neuroscience and Neural Engineering
  • RNA Research and Splicing
  • Cardiac electrophysiology and arrhythmias
  • Mesenchymal stem cell research
  • Cardiac Structural Anomalies and Repair
  • Cardiac Imaging and Diagnostics
  • Cardiovascular Function and Risk Factors
  • Cardiovascular Effects of Exercise
  • Mitochondrial Function and Pathology
  • Biomedical Ethics and Regulation
  • Cardiac Fibrosis and Remodeling
  • Genomics and Chromatin Dynamics
  • Single-cell and spatial transcriptomics
  • Cardiac Arrest and Resuscitation
  • RNA Interference and Gene Delivery
  • Viral Infections and Immunology Research

University of Washington
2015-2024

Southern California University for Professional Studies
2024

University of Southern California
2024

California Institute for Regenerative Medicine
2008-2023

Sana Biotechnology (United States)
2020-2023

Seattle University
1991-2023

Institute for Stem Cell Biology and Regenerative Medicine
2011-2022

Cardiovascular Research Center
2011-2021

Harvard University
2005-2017

Max Planck Institute for Heart and Lung Research
2017

We have previously shown that a brief episode of ischemia slows the rate ATP depletion during subsequent ischemic episodes. Additionally, intermittent reperfusion may be beneficial to myocardium by washing out catabolites accumulated ischemia. Thus, we proposed multiple episodes might actually protect heart from sustained insult. To test this hypothesis, two sets experiments were performed. In first set, one group dogs (n = 7) was preconditioned with four 5 min circumflex occlusions, each...

10.1161/01.cir.74.5.1124 article EN Circulation 1986-11-01

Abstract —Vascular calcification is a common finding in atherosclerosis and serious problem diabetic uremic patients. Because of the correlation hyperphosphatemia vascular calcification, ability extracellular inorganic phosphate levels to regulate human aortic smooth muscle cell (HSMC) culture mineralization vitro was examined. HSMCs cultured media containing normal physiological (1.4 mmol/L) did not mineralize. In contrast, comparable those seen hyperphosphatemic individuals (>1.4 showed...

10.1161/01.res.87.7.e10 article EN Circulation Research 2000-09-29

We have shown previously that preconditioning myocardium with four 5-minute episodes of ischemia and reperfusion dramatically limited the size infarcts caused by a subsequent 40-minute episode sustained ischemia. The current study was undertaken to assess whether same protocol slowed loss high energy phosphates, catabolite accumulation, and/or delayed ultrastructural damage during ischemic episode. Myocardial metabolites ultrastructure in severely subendocardial regions were compared between...

10.1161/01.res.66.4.913 article EN Circulation Research 1990-04-01

ABSTRACT Embryonic stem (ES) cells are promising for cardiac repair’ but directing their differentiation toward cardiomyocytes remains challenging. We investigated whether the heart guides ES in vivo and allogeneic were immunologically tolerated. Undifferentiated mouse consistently formed teratomas nude or immunocompetent syngeneic mice. Cardiac contained no more than hind‐limb teratomas’ suggesting lack of guided differentiation. also infarcted hearts’ indicating injury‐related signals did...

10.1096/fj.06-6769com article EN The FASEB Journal 2007-02-06

Rationale: The developing heart requires both mechanical load and vascularization to reach its proper size, yet the regulation of human growth by these processes is poorly understood. Objective: We seek elucidate responses immature myocardium using tissue engineering approaches. Methods Results: Using embryonic stem cell induced pluripotent cell–derived cardiomyocytes in a 3-dimensional collagen matrix, we show that uniaxial stress conditioning promotes 2-fold increases cardiomyocyte matrix...

10.1161/circresaha.110.237206 article EN Circulation Research 2011-05-20

We demonstrate here a cardiac tissue-engineering strategy addressing multicellular organization, integration into host myocardium, and directional cues to reconstruct the functional architecture of heart muscle. Microtemplating is used shape poly(2-hydroxyethyl methacrylate-co-methacrylic acid) hydrogel scaffold with architectures driving tissue integration. The construct contains parallel channels organize cardiomyocyte bundles, supported by micrometer-sized, spherical, interconnected pores...

10.1073/pnas.1006442107 article EN Proceedings of the National Academy of Sciences 2010-08-09

Myocardial infarcts heal by scarring because myocardium cannot regenerate. To determine if skeletal myoblasts could establish new contractile tissue, hearts of adult inbred rats were injured freeze-thaw, and 3-4.5 x 10(6) neonatal muscle cells transplanted immediately thereafter. At 1 d the graft proliferating did not express myosin heavy chain (MHC). By 3 d, multinucleated myotubes present which expressed both embryonic fast fiber MHCs. 2 wk, electron microscopy demonstrated possible...

10.1172/jci119070 article EN Journal of Clinical Investigation 1996-12-01

Understanding pathways controlling cardiac development may offer insights that are useful for stem cell-based repair. Developmental studies indicate the Wnt/β-catenin pathway negatively regulates differentiation, whereas with pluripotent embryonal carcinoma cells suggest this promotes cardiogenesis. This apparent contradiction led us to hypothesize signaling acts biphasically, either promoting or inhibiting cardiogenesis depending on timing. We used inducible promoters activate repress in...

10.1073/pnas.0702859104 article EN Proceedings of the National Academy of Sciences 2007-05-24

The pervasive expression of circular RNA is a recently discovered feature gene in highly diverged eukaryotes, but the functions most RNAs are still unknown. Computational methods to discover and quantify essential. Moreover, discovering biological contexts where regulated will shed light on potential functional roles they may play.We present new algorithm that increases sensitivity specificity detection by quantifying linear splicing events at both annotated un-annotated exon boundaries,...

10.1186/s13059-015-0690-5 article EN cc-by Genome biology 2015-06-15

Background —Cardiomyocyte grafting augments myocyte numbers in the heart. We investigated (1) how developmental stage influences graft survival; (2) whether acutely necrotic or healing cardiac lesions support grafts; and (3) differentiation integration of cardiomyocyte grafts injured hearts. Methods Results —Cardiomyocytes from fetal, neonatal, adult inbred rats were grafted into normal myocardium, cryoinjured granulation tissue (6 days after injury). Adult cardiomyocytes did not survive...

10.1161/01.cir.100.2.193 article EN Circulation 1999-07-13
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