Resumen
Transferrin receptor 1 (TfR1), a crucial cellular iron receptor, has a variety of biological functions. We have previously reported that TfR1 abundance increases in the aortic media of hypertensive rat models. However, its role in vascular diseases remains unknown. In the present study, we generated smooth muscle cell (SMC)-specific TfR1 deficient mice and examined the impact of its deletion in mouse models of hypertension induced by angiotensin II or deoxycorticosterone acetate/salt administration. SMC-specific TfR1 deletion attenuated medial thickening and elastin fragmentation in both mouse models of hypertension. These results indicate that TfR1 in SMCs exerts a role in vascular remodeling in hypertension. (Figure presented.)
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 2263-2268 |
| Número de páginas | 6 |
| Publicación | Hypertension Research |
| Volumen | 48 |
| N.º | 8 |
| DOI | |
| Estado | Published - ago 2025 |
Nota bibliográfica
Publisher Copyright:© The Author(s) 2025.
Financiación
This work was supported by a Grant-in-Aid for Scientific Research (C) JSPS KAKENHI (#25460919, #16K09273, #19K07950, #22K07408) and grants from The Salt Science Research Foundation (#1544, #1641, #1826, and #2134) to Naito Y.
| Financiadores | Número del financiador |
|---|---|
| Japan Society for the Promotion of Science | 22K07408, 25460919, 16K09273, 19K07950 |
| Salt Science Research Foundation | 1544, 1641, 2134, 1826 |
ASJC Scopus subject areas
- Internal Medicine
- Physiology
- Cardiology and Cardiovascular Medicine
Huella
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