Literature DB >> 34865504

BBSome: a New Player in Hypertension and Other Cardiovascular Risks.

Yuying Zhao1,2, Kamal Rahmouni1,3,4,5,6.   

Abstract

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.

Entities:  

Keywords:  Bardet-Biedl syndrome; blood pressure; heart disease; kidney disease; obesity

Mesh:

Year:  2021        PMID: 34865504      PMCID: PMC8755612          DOI: 10.1161/HYPERTENSIONAHA.121.17946

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  80 in total

1.  Basal body proteins regulate Notch signaling through endosomal trafficking.

Authors:  Carmen C Leitch; Sukanya Lodh; Victoria Prieto-Echagüe; Jose L Badano; Norann A Zaghloul
Journal:  J Cell Sci       Date:  2014-03-28       Impact factor: 5.285

Review 2.  The primary cilium as the cell's antenna: signaling at a sensory organelle.

Authors:  Veena Singla; Jeremy F Reiter
Journal:  Science       Date:  2006-08-04       Impact factor: 47.728

3.  Differences in renal tubule primary cilia length in a mouse model of Bardet-Biedl syndrome.

Authors:  Elaine M Mokrzan; Jacqueline S Lewis; Kirk Mykytyn
Journal:  Nephron Exp Nephrol       Date:  2007-05-22

4.  BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human development.

Authors:  K Bénardais; G Delfino; B Samama; D Devys; M C Antal; M S Ghandour; N Boehm
Journal:  Cell Tissue Res       Date:  2021-04-16       Impact factor: 5.249

5.  Photoreceptor cilia, in contrast to primary cilia, grant entry to a partially assembled BBSome.

Authors:  Ying Hsu; Seongjin Seo; Val C Sheffield
Journal:  Hum Mol Genet       Date:  2021-03-25       Impact factor: 6.150

6.  Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS).

Authors:  Kim M Keppler-Noreuil; Catherine Blumhorst; Julie C Sapp; Danielle Brinckman; Jennifer Johnston; Peggy C Nopoulos; Leslie G Biesecker
Journal:  BMC Med Genet       Date:  2011-07-27       Impact factor: 2.103

7.  Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome.

Authors:  Qihong Zhang; Dahai Yu; Seongjin Seo; Edwin M Stone; Val C Sheffield
Journal:  J Biol Chem       Date:  2012-04-12       Impact factor: 5.157

8.  Bardet-Biedl syndrome proteins control the cilia length through regulation of actin polymerization.

Authors:  Victor Hernandez-Hernandez; Priyanka Pravincumar; Anna Diaz-Font; Helen May-Simera; Dagan Jenkins; Martin Knight; Philip L Beales
Journal:  Hum Mol Genet       Date:  2013-05-27       Impact factor: 6.150

9.  Restoration of renal function in zebrafish models of ciliopathies.

Authors:  Jonathan L Tobin; Philip L Beales
Journal:  Pediatr Nephrol       Date:  2008-07-05       Impact factor: 3.714

10.  Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators.

Authors:  Yangfan P Liu; I-Chun Tsai; Manuela Morleo; Edwin C Oh; Carmen C Leitch; Filomena Massa; Byung-Hoon Lee; David S Parker; Daniel Finley; Norann A Zaghloul; Brunella Franco; Nicholas Katsanis
Journal:  J Clin Invest       Date:  2014-04-01       Impact factor: 14.808

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