Cedars-Sinai investigators used protein mapping to study the differences between naturally occurring heart cells and those created from stem cells鈥攖he latter illustrated here.
Newswise — LOS ANGELES (March 3, 2025) -- A multidisciplinary team of investigators has used a novel single-cell proteomics approach to better understand the differences between naturally occurring adult heart cells and heart cells derived from induced pluripotent stem cells. Their work created one of the largest and most detailed single-cell protein datasets to date and was published in the peer-reviewed journal . The data could lead to improvements in how scientists study heart conditions and develop treatments.
Senior authors of the study were Jennifer Van Eyk, PhD, director of Basic Science Research in the Barbra Streisand Women’s Heart Center; Clive Svendsen, PhD, executive director of the Board of Governors Regenerative Medicine Institute; and Eduardo Marbán, MD, PhD, executive director of the Smidt Heart Institute. The work was spearheaded by postdoctoral scientists Lizhuo Ai and Vladimir Zhemkov.
Investigators tracked protein changes in individual cells as they developed from stem cells into heart cells, and revealed important differences in the structure and metabolism of these cells as compared with naturally occurring heart cells. While single-cell RNA methods are widely available now and allow thousands of genes to be assessed simultaneously, there is very little data looking at the inventory of proteins within single cells simultaneously. Cedars-Sinai is pioneering new single-cell technologies at its Innovation Center and using the most advanced protein analysis equipment to get more resolution of proteins within single cells for the first time.
“We looked at cardiomyocytes, which are heart muscle cells,” said Aleksandra Binek, PhD, project scientist and co-first author of the study. “We discovered two distinct types of cardiomyocytes and found rare hybrid cells expressing both heart- and neuron-related proteins, suggesting that heart cells may have more protein flexibility than previously thought. These discoveries will help us create more detailed, realistic models of human heart cells.”
Additional authors: Jae Hyung Cho, Ali Haghani, Simion Kreimer, Edo Israely, Madelyn Arzt, Blandine Chazarin, Niveda Sundararaman, Arun Sharma
Funding: This work was supported by NIH R01 HL144509-01 (JVE) and R01 HL155346-01 (JVE/EM). Lizhuo Ai and Vladimir Zhemkov were supported by the California Institute for Regenerative Medicine (CIRM) Scholar Training Program (CIRM EDUC4-12751). Arun Sharma and Madelyn Arzt were supported by American Heart Association Career Development Award (AHA 856987). Clive Svendsen and Arun Sharma were supported by NASA In Space Production Award (NASA NNJ13ZBG001N).
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