BRIEF RESEARCH REPORT article

Front. Cell Dev. Biol.

Sec. Morphogenesis and Patterning

Temporal Expression Dynamics of Glypicans During hiPSC Cardiac Differentiation

  • 1. Regenerative Medicine Research, The Texas Heart Institute at Baylor College of Medicine, Houston, Texas, USA, Houston, United States

  • 2. Michael E. Debakey Department of Surgery, Baylor College of Medicine, Houston, United States

  • 3. McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA, Houston, United States

  • 4. Department of Internal Medicine, Division of Pulmonary, Critical Care & Sleep Medicine, College of Medicine, University of Arizona, Phoenix, Arizona, USA, Phoenix, United States

  • 5. Biofluid Repository Core, Baylor College of Medicine Dan L Duncan Comprehensive Cancer Center, Houston, United States

The final, formatted version of the article will be published soon.

Abstract

Human pluripotent stem cells (hPSCs) offer a versatile platform for modeling human cardiac development and generating cardiomyocytes for research and translational applications. Cardiac differentiation protocols are well established and rely on the sequential activation and inhibition of WNT, BMP, and FGF signaling pathways to guide lineage progression. While these intracellular signaling events are well characterized, less attention has been given to the temporal behavior of extracellular components present at the cell surface during differentiation. Glypicans (GPCs) are a family of membrane-bound heparan sulfate proteoglycans within the glycocalyx that are known to interact with morphogens in multiple developmental contexts. In this study, we profiled the expression of GPC1-6 during a standard chemically defined cardiac differentiation protocol, in the absence of targeted interventions. Gene expression analysis across stages revealed distinct, stage-associated patterns: GPC3 and GPC6 were upregulated during the WNT activation phase; GPC4 was suppressed after WNT inhibition and maintained low during cardiac commitment. GPC2 and GPC5 expressions peaked during the formation of cardiac progenitors, and GPC1 expression increased following cardiac specification. These findings provide a temporal map of GPC expression coinciding with established differentiation stages, demonstrating that members of the glypican family are dynamically expressed during human cardiac differentiation. By documenting when specific glypicans are expressed during a commonly used differentiation workflow, this study offers a descriptive reference framework that may inform future mechanistic studies investigating how extracellular components intersect with canonical cardiac signaling pathways.

Summary

Keywords

cardiac differentiation, Dynamic expression, Gene Expression, Glypicans, Human pluripotent stem cells

Received

31 December 2025

Accepted

18 February 2026

Copyright

© 2026 Mesquita, Kim, Chignalia and Hochman-Mendez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Camila Hochman-Mendez

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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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