Conditional Deletion of Bmal1 Accentuates Microvascular and Macrovascular Injury

Ashay Bhatwadekar, Eleni Beli, Yanpeng Diao, Jonathan Chen, Qianyi Luo, Alpha Alex, Sergio Caballero, James M. Dominguez, Tatiana E. Salazar, Julia V. Busik, Mark S. Segal, Maria B. Grant

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The brain and muscle aryl hydrocarbon receptor nuclear translocator–like protein (BMAL)-1 constitutes a major transcriptional regulator of the circadian clock. Here, we explored the impact of conditional deletion of Bmal1 in endothelium and hematopoietic cells in murine models of microvascular and macrovascular injury. We used two models of Bmal1fx/fx;Tek-Cre mice, a retinal ischemia/reperfusion model and a neointimal hyperplasia model of the femoral artery. Eyes were enumerated for acellular capillaries and were stained for oxidative damage markers using nitrotyrosine immunohistochemistry. LSK (lineage-negative, stem cell antigen-1–positive, c-Kit–positive) cells were quantified and proliferation assessed. Hematopoiesis is influenced by innervation to the bone marrow, which we assessed using IHC analysis. The number of acellular capillaries increased threefold, and nitrotyrosine staining increased 1.5-fold, in the retinas of Bmal1fx/fx;Tek-Cre mice. The number of LSK cells from the Bmal1fx/fx;Tek-Cre mice decreased by 1.5-fold and was accompanied by a profound decrease in proliferative potential. Bmal1fx/fx;Tek-Cre mice also exhibited evidence of bone marrow denervation, demonstrating a loss of neurofilament-200 staining. Injured femoral arteries showed a 20% increase in neointimal hyperplasia compared with similarly injured wild-type controls. Our study highlights the importance of the circadian clock in maintaining vascular homeostasis and demonstrates that specific deletion of BMAL1 in endothelial and hematopoietic cells results in phenotypic features similar to those of diabetes.

Original languageEnglish (US)
Pages (from-to)1426-1435
Number of pages10
JournalAmerican Journal of Pathology
Volume187
Issue number6
DOIs
StatePublished - Jun 1 2017

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Circadian Clocks
Wounds and Injuries
Femoral Artery
Hyperplasia
Bone Marrow
Staining and Labeling
Aryl Hydrocarbon Receptors
Hematopoiesis
Denervation
Nuclear Proteins
Reperfusion
Endothelium
Blood Vessels
Retina
Homeostasis
Stem Cells
Ischemia
Endothelial Cells
Cell Count
Immunohistochemistry

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Conditional Deletion of Bmal1 Accentuates Microvascular and Macrovascular Injury. / Bhatwadekar, Ashay; Beli, Eleni; Diao, Yanpeng; Chen, Jonathan; Luo, Qianyi; Alex, Alpha; Caballero, Sergio; Dominguez, James M.; Salazar, Tatiana E.; Busik, Julia V.; Segal, Mark S.; Grant, Maria B.

In: American Journal of Pathology, Vol. 187, No. 6, 01.06.2017, p. 1426-1435.

Research output: Contribution to journalArticle

Bhatwadekar, A, Beli, E, Diao, Y, Chen, J, Luo, Q, Alex, A, Caballero, S, Dominguez, JM, Salazar, TE, Busik, JV, Segal, MS & Grant, MB 2017, 'Conditional Deletion of Bmal1 Accentuates Microvascular and Macrovascular Injury', American Journal of Pathology, vol. 187, no. 6, pp. 1426-1435. https://doi.org/10.1016/j.ajpath.2017.02.014
Bhatwadekar, Ashay ; Beli, Eleni ; Diao, Yanpeng ; Chen, Jonathan ; Luo, Qianyi ; Alex, Alpha ; Caballero, Sergio ; Dominguez, James M. ; Salazar, Tatiana E. ; Busik, Julia V. ; Segal, Mark S. ; Grant, Maria B. / Conditional Deletion of Bmal1 Accentuates Microvascular and Macrovascular Injury. In: American Journal of Pathology. 2017 ; Vol. 187, No. 6. pp. 1426-1435.
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