4.5 Article

Adrenomedullin-RAMP2 and-RAMP3 Systems Regulate Cardiac Homeostasis during Cardiovascular Stress

Journal

ENDOCRINOLOGY
Volume 162, Issue 3, Pages -

Publisher

ENDOCRINE SOC
DOI: 10.1210/endocr/bqab001

Keywords

adrenomedullin; heart failure; cardiac hypertrophy; cardiac fibrosis; mitochondria; lymphatic vessel

Funding

  1. JSPS KAKENHI [18H02602]
  2. Grants-in-Aid for Scientific Research [18H02602] Funding Source: KAKEN

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The AM-RAMP2 system is crucial for early adaptation to cardiovascular stress in the heart, regulating cardiac mitochondria function. On the other hand, the AM-RAMP3 system plays a critical role in long-term adaptation by regulating lymphatic vessels in the heart. Both systems are essential for maintaining cardiovascular homeostasis against stress.
Adrenomedullin (AM) is a peptide hormone with multiple physiological functions, which are regulated by its receptor activity-modifying proteins, RAMP2 and RAMP3. We previously reported that AM or RAMP2 knockout (KO) (AM-/-, RAMP2-/-) is embryonically lethal in mice, whereas RAMP3-/- mice are apparently normal. AM, RAMP2, and RAMP3 are all highly expressed in the heart; however, their functions there are not fully understood. Here, we analyzed the pathophysiological functions of the AM-RAMP2 and AM-RAMP3 systems in hearts subjected to cardiovascular stress. Cardiomyocyte-specific RAMP2-/- (C-RAMP2-/-) and RAMP3-/- showed no apparent heart failure at base line. After 1 week of transverse aortic constriction (TAC), however, C-RAMP2-/- exhibited significant cardiac hypertrophy, decreased ejection fraction, and increased fibrosis compared with wild-type mice. Both dP/dtmax and dP/dtmin were significantly reduced in C-RAMP2-/-, indicating reduced ventricular contractility and relaxation. Exposing C-RAMP2-/- cardiomyocytes to isoproterenol enhanced their hypertrophy and oxidative stress compared with wild-type cells. C-RAMP2-/- cardiomyocytes also contained fewer viable mitochondria and showed reduced mitochondria! membrane potential and respiratory capacity. RAMP3-/- also showed reduced systolic function and enhanced fibrosis after TAC, but those only became apparent after 4 weeks. A reduction in cardiac lymphatic vessels was the characteristic feature in RAMP3-/-. These observations indicate the AM-RAMP2 system is necessary for early adaptation to cardiovascular stress through regulation of cardiac mitochondria. AM-RAMP3 is necessary for later adaptation through regulation of lymphatic vessels. The AM-RAMP2 and AM-RAMP3 systems thus play separate critical roles in the maintenance of cardiovascular homeostasis against cardiovascular stress.

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