PIPages
Labs

Brenda Ogle

University of Minnesota, MN·Biomedical Engineering

Heart muscle cells grown from human stem cells could be used to model heart disease, test drugs and devices, and perhaps someday repair damaged hearts. A major barrier is that these lab-grown cells stay immature.

Fields

Biomedical Engineering

Engineering

Physiology

Topics

cardiac tissue engineering

cardiomyocytes

hPSC-CMs

Grants
2 known grants, through May 2030

What they work on

  1. Identify growth factors secreted by epicardial progenitor cells that boost proliferation of hiPSC-derived heart muscle cells, using gene editing and high-throughput proteomics in a 3D-printed layered cardiac tissue.
  2. Determine which ECM proteins secreted by epicardial-derived cells drive structural and functional maturation of engineered human cardiac tissue.
  3. Add an epicardial layer to a 3D-printed chambered myocardial pump and measure stroke work and ejection fraction with and without imposed volumetric pressure.
  4. Develop and validate a computational fluid-structure interaction model that reproduces native cardiac pressure profiles in the epi-hChaMP chambered muscle pump.
  5. Test how cardiac fibroblasts remodel the ECM under physiologic loading to drive heart muscle cell maturation, and use statistical optimization to define loading regimes that maximize maturation.

More about the research

They behave more like embryonic cells than adult heart muscle, and tissues made from them are thin and weak. The lab's work explores how signals from neighboring cells and from the extracellular matrix (ECM), the protein scaffold around cells, can drive these cells to mature. It also builds a 3D-printed, chambered human heart-muscle pump to study this.

Why it matters

More mature, lab-grown human heart tissue could provide better models for studying heart disease and for testing drugs and medical devices. This is especially useful for conditions that alter pressure-volume dynamics. In the longer term, a living human muscle pump grown in a dish might be used to help restore heart function in patients with heart disease.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Evolving extracellular matrices evoke signaling pathways that govern cardiomyocyte maturation

NIH · Jul 2026 – May 2030

Epicardial regulation of cardiomyocyte function via modulation of extracellular signals: toward a model of human muscle pump function

NIH · Jul 2022 – Jun 2027

Closest labs

Forum Kamdar

University of Minnesota, MN·Biomedical Engineering·Early-career

Build 3D-bioprinted human chambered muscle pumps (hChaMPs) from DMD patient stem cell-derived heart cells and test how progressively increasing pressure alters mechanotransduction and heart function at early and later disease stages.

Ryan Stowers

University of California-Santa Barbara, CA·Biomedical Engineering

Determine whether cardiomyopathy-driven remodeling of the extracellular matrix alters myocardial viscoelasticity, by mechanically testing human DCM and HCM heart tissue and pig disease-model tissue.

Miqin Zhang

University of Washington, WA·Biomedical Engineering

Test how the composition and stiffness of chitosan–alginate (CA) scaffolds control human induced pluripotent stem cell self-renewal, and whether optimized scaffolds support long-term growth of tooth epithelial stem cells and neural crest cells.

The school

University of Minnesota: 88 labs on PI Pages, $1.4B a year on research, 722 research doctorates a year.

More about University of Minnesota

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