Lowering cost of heart cell therapies

Kyoto University

A T-CiRA’s project, led by CiRA’s Yoshinori Yoshida, finds that the activation of a single molecule enhances the quality of heart cells made from iPS cells.

Suffering from the number one cause of death, patients with heart disease are in desperate need of new therapies. However, these new therapies rely on research using heart cells, which are not easy to access. In response, many scientists are investigating ways to generate heart cells from stem cells like iPS cells. A new study led by researchers of Takeda-CiRA Joint Program for iPS Cell Applications (T-CiRA) shows how mixing a single agonist for ERRγ, or estrogen-related receptor gamma, with iPS cells can produce cardiomyocytes of good quality. The findings are expected to lower the cost and labour of future heart cell research.

One of the most exciting clinical applications of stem cell research is heart therapy. Among all cells in the body, heart cells are the least capable of regenerating, which is why heart disease or heart damage is usually permanent. Heart transplants and cell therapies are the only viable treatment options, but neither whole hearts nor heart cells are readily available. Stem cells, especially iPS cells, offer a solution.

However, the heart cells made from stem cells are not equivalent to those in the heart.

“We can differentiate iPS cells into cardiomyocytes, but the cells are structurally and functionally immature, resembling heart cells in the fetus,” explained Dr. Kenji Miki, one of the lead authors of the study. “The cells are structurally and functionally immature, resembling heart cells in the fetus but not the adult.”

This difference has important implications in the search for new drugs and new therapies.

The maturity of heart cells depends on a number of morphological and molecular events. One that scientists regularly rely on involves the protein troponin I.

“During the developmental transition from fetal to postnatal stages, troponin I undergoes an isoform switch from TNNI1 to TNNI3. This change is accompanied by electrophysiological changes in the heart,” said CiRA Associate Professor Yoshinori Yoshida, who led the study. “We look for this switch when differentiating iPS cells into cardiomyocytes.”

The study shows that a single ERRγ agonist promotes the isoform switch in cardiomyocytes made from iPS cells and the formation of T-tubules, a key structural indicator of maturation. ERRγ is a hormone receptor that switches the metabolism of mouse cells to oxidative phosphorylation, but its role in humans is not as clear and requires more study.

Along with the structural and functional changes that are marked by the transition to TNNI3, cardiomyocytes undergo a change in metabolism during development. ATP is generated by one of two ways in all cells, glycolysis and oxidative phosphorylation. In the uterus, where oxygen levels are low, fetal cardiomyocytes depend on anaerobic glycolysis. However, the amount of ATP produced by aerobic oxidative phosphorylation is much higher, which is what adult cardiomyocytes primarily use.

The ERRγ agonist supported this metabolic switch.

Maturation could be further promoted by adding to the agonist a chemical inhibitor of the cell cycle. The cell cycle is a natural process that allows cells to replicate. Heart cells, however, show cell cycle arrest, which is why they do not regenerate following injury.

“Our findings suggest that ERRγ has an important role in cardiomyocyte maturation. This discovery will help in establishing protocols that produce high quality cardiomyocytes for disease modeling, drug discovery and cell therapies,” said Yoshida.

Paper Details
  • Journal: Nature Communications
  • Title: ERRγ enhances cardiac maturation with T-tubule formation in human iPSC-derived cardiomyocytes
  • Authors:
    Kenji Miki1,2*, Kohei Deguchi2,3*, Misato Nakanishi-Koakutsu1,2*, Antonio Lucena-Cacace1, Shigeru Kondo2,3, Yuya Fujiwara1,2, Takeshi Hatani1, Masako Sasaki1,2, Yuki Naka1,2, Chikako Okubo1, Megumi Narita1, Ikue Takei1,2, Stephanie C Napier2,3,
    Tsukasa Sugo4, Sachiko Imaichi5, Taku Monjo6, Tatsuya Ando6, Norihisa Tamura2,3, Kenichi Imahashi2,3, Tomoyuki Nishimoto2,3, and Yoshinori Yoshida1,2

    *These authors contributed equally to this work.

  • Author Affiliations:
    1. Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan
    2. Takeda-CiRA Joint program (T-CiRA), Fujisawa, Japan
    3. T-CiRA Discovery, Takeda Pharmaceutical Company Limited, Fujisawa, Japan
    4. GenAhead Bio Inc., Fujisawa, Japan
    5. Pharmaceutical Science, Takeda Pharmaceutical Company Limited, Fujisawa, Japan
    6. IBL, Takeda Pharmaceutical Company Limited, Fujisawa, Japan

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