BCL11B Regulates Arterial Stiffness and Related Target Organ Damage

Author:

Valisno Jeff Arni C.1,May Joel1,Singh Kuldeep2,Helm Eric Y.3,Venegas Lisia1,Budbazar Enkhjargal1,Goodman Jena B.1,Nicholson Christopher J.2,Avram Dorina34,Cohen Richard A.1,Mitchell Gary F.5ORCID,Morgan Kathleen G.2ORCID,Seta Francesca1ORCID

Affiliation:

1. Vascular Biology Section, Department of Medicine, Boston University School of Medicine, MA (J.A.C.V., J.M., L.V., E.B., J.B.G., R.A.C., F.S.).

2. Department of Health Sciences, Sargent College, Boston University, MA (K.S., C.J.N., K.G.M.).

3. Department of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville (E.Y.H., D.A.).

4. Department of Immunology, Moffitt Cancer Center, Tampa, FL (D.A.).

5. Cardiovascular Engineering, Norwood, MA (G.F.M.).

Abstract

Rationale:BCL11B (B-cell leukemia 11b) is a transcription factor known as an essential regulator of T lymphocytes and neuronal development during embryogenesis. A genome-wide association study showed that a gene desert region downstream ofBCL11B, known to function as aBCL11Benhancer, harbors single nucleotide polymorphisms associated with increased arterial stiffness. However, a role for BCL11B in the adult cardiovascular system is unknown.Objective:Based on these human findings, we sought to examine the relation between BCL11B and arterial function.Methods and Results:Here we report that BCL11B is expressed in the vascular smooth muscle where it regulates vascular stiffness. RNA sequencing of aortas from wild-type andBcl11bnull mice (BSMKO) identified the cGMP (cyclic guanosine monophosphate)-cGMP-dependent protein kinase G (PKG) as the most significant differentially regulated signaling pathway in BSMKO compared with wild-type mice. BSMKO aortas showed decreased levels of PKG1, increased levels of Ca++-calmodulin-dependent serine/threonine phosphatase calcineurin (PP2B) and decreased levels of their common phosphorylation target, phosphorylated vasodilator-stimulated phosphoprotein (pVASPS239), a regulator of cytoskelatal actin rearrangements. Decreased pVASPS239in BSMKO aortas was associated with increased actin polymerization (filamentous/globular actin ratio). Functionally, aortic force, stress, wall tension, and stiffness, measured ex vivo in organ baths, were increased in BSMKO aortas, and BSMKO mice had increased pulse wave velocity, the in vivo index of arterial stiffness. Despite having no effect on blood pressure or microalbuminuria, increased arterial stiffness in BSMKO mice was associated with increased incidence of cerebral microbleeds compared with age-matched wild-type littermates.Conclusions:We have identified vascular smooth muscle BCL11B as a crucial regulator of aortic smooth muscle function and a potential therapeutic target for vascular stiffness.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute on Aging

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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