BBSome: a New Player in Hypertension and Other Cardiovascular Risks.
Yuying ZhaoKamal RahmouniPublished in: Hypertension (Dallas, Tex. : 1979) (2021)
The BBSome is an octameric protein complex involved in Bardet-Biedl syndrome (BBS), a human pleiotropic, autosomal recessive condition. Patients with BBS display various clinical features including obesity, hypertension, and renal abnormalities. Association studies have also linked the BBS genes to hypertension and other cardiovascular risks in the general population. The BBSome was originally associated with the function of cilia, a highly specialized organelle that extend from the cell membrane of most vertebrate cells. However, subsequent studies have implicated the BBSome in the control of a myriad of other cellular processes not related to cilia including cell membrane localization of receptors and gene expression. The development of animal models of BBS such as mouse lines lacking various components of the BBSome and associated proteins has facilitated studying their role in the control of cardiovascular function and deciphering the pathophysiological mechanisms responsible for the cardiovascular aberrations associated with BBS. These studies revealed the importance of the neuronal, renal, vascular, and cardiac BBSome in the regulation of blood pressure, renal function, vascular reactivity, and cardiac development. The BBSome has also emerged as a critical regulator of key systems involved in cardiovascular control including the renin-angiotensin system. Better understanding of the influence of the BBSome on the molecular and physiological processes relevant to cardiovascular health and disease has the potential of identifying novel mechanisms underlying hypertension and other cardiovascular risks.
Keyphrases
- blood pressure
- gene expression
- human health
- hypertensive patients
- heart rate
- endothelial cells
- metabolic syndrome
- induced apoptosis
- insulin resistance
- physical activity
- heart failure
- palliative care
- risk assessment
- single cell
- adipose tissue
- atrial fibrillation
- brain injury
- cell death
- amino acid
- case report
- binding protein
- endoplasmic reticulum stress
- cell proliferation
- cell cycle arrest
- protein protein
- cerebral ischemia