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Updated: Sep 28, 2025

An Intact Pericardium Ischemic Rodent Model
Published on: September 2, 2021
The G Protein-Coupled Receptor Latrophilin-2, A Marker for Heart Development, Induces Myocardial Repair After
Choon-Soo Lee1,2, Hyun-Jai Cho3, Jin-Woo Lee1,2
1Strategic Center of Cell & Bio Therapy, Seoul National University Hospital, Seoul, South Korea.
Latrophilin-2 (Lphn2) is crucial for heart development and repair. Identifying Lphn2+ cells enables targeted stem cell therapy for cardiac regeneration, improving heart function after infarction.
Area of Science:
- Cardiovascular Biology
- Developmental Biology
- Regenerative Medicine
Background:
- Identifying specific cell-surface markers is key for isolating pure cell populations for therapeutic applications.
- Latrophilin-2 (Lphn2) is known to play a role in cardiac differentiation.
Purpose of the Study:
- To investigate the role of Lphn2 in heart development and repair.
- To evaluate Lphn2 as a potential cardiomyogenic marker for cardiac regeneration therapies.
Main Methods:
- Whole-mount immunostaining and clearing of embryos.
- RNA sequencing of Lphn2-knockout (KO) embryos.
- In vivo functional analysis of Lphn2+ cells using echocardiography.
- Transplantation of pluripotent stem cell (PSC)-derived Lphn2+ cells into infarcted hearts.
Main Results:
- Lphn2 is exclusively expressed in cardiac cells during embryonic development (E9.5-E10.5).
- Lphn2-KO mice exhibit embryonic lethality and underdeveloped ventricular myocardium.
- Transplanted PSC-derived Lphn2+ cells differentiate into cardiomyocytes, regenerate myocardium, improve cardiac function, and reduce infarct size in vivo.
- Lphn2 is not essential for vascular development.
Conclusions:
- Lphn2 is a critical regulator of heart development and a promising cardiomyogenic marker.
- Targeting Lphn2+ cells holds potential for effective stem cell therapy in clinical heart repair.
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