The regulation of leukocyte infiltration into tissues is a crucial parameter of the immune response. Circadian manifestations of vascular diseases, including ischemic vasculopathies and sickle cell disease, have been well documented. Although diurnal variations in blood leukocyte counts have been reported, whether leukocyte recruitment is influenced by circadian rhythms is unclear. In addition, the identification of the cell subsets involved and the mechanisms that regulate the circadian oscillations in leukocyte behavior is not understood. Greater understanding in this area will help to unravel the physiological and pathophysiological relevance of these endogenous rhythms in vascular biology. We have recently found that hematopoietic stem cells are released from the bone marrow (BM) through circadian regulation by rhythmic signals delivered locally in the BM microenvironment by the sympathetic nervous system (SNS) via the ?3 adrenergic receptor (Mendez-Ferrer et al. Nature, 2008). Our preliminary studies using real-time multichannel fluorescence intravital microscopy (MFIM) have revealed that leukocyte-endothelial cell interactions are increased at night in mice resulting in enhanced leukocyte recruitment in tissues. Furthermore, using chemical sympathectomy and surgical denervation, we have found that the fluctuations of leukocyte recruitment were abolished in mice with an impaired SNS and were dependent on the fluctuations of endothelial selectins in the BM. These studies have led us to hypothesize that the circadian fluctuations in leukocyte recruitment to peripheral tissues are regulated by oscillations in endothelial cell adhesion molecule expression that is controlled by the SNS. This hypothesis will be tested in three Specific Aims.
In Specific Aim 1, we will identify which leukocyte populations exhibit circadian fluctuations in the BM, cremaster muscle and dermal tissues under homeostatic conditions using brightfield and MFIM techniques for the real-time in vivo evaluation of leukocyte-endothelial interactions, with whole-mount ex vivo immunofluorescence imaging, and flow cytometry analyses.
In Specific Aim 2, we will define the mechanisms regulating the circadian oscillations in leukocyte recruitment. We will identify the promigratory molecules and assess the mechanisms implementating these circadian rhythms, focusing on the role of the SNS and adrenergic receptors using surgical, pharmacological and genetic approaches.
In Specific Aim 3, we will investigate whether circadian rhythms of leukocyte trafficking influence the inflammatory response in models of acute and chronic inflammation. The results generated from this proposal will enhance our basic understanding of this important biological phenomenon, and will likely identify novel chronotherapeutic targets for interventions in inflammatory diseases.

Public Health Relevance

Specific circadian timing can dictate the clinical manifestations or onset of vascular diseases. Here, we will identify the leukocyte populations that exhibit circadian fluctuations, elucidate the underlying mechanisms, and investigate how these rhythms influence acute and chronic inflammatory responses. The results generated from this proposal will enhance our basic understanding of this important biological phenomenon, and identify novel chronotherapeutic targets for interventions in inflammatory diseases.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL097700-04
Application #
8301648
Study Section
Special Emphasis Panel (ZHL1-CSR-N (S1))
Program Officer
Laposky, Aaron D
Project Start
2009-09-15
Project End
2014-07-31
Budget Start
2012-08-01
Budget End
2014-07-31
Support Year
4
Fiscal Year
2012
Total Cost
$410,850
Indirect Cost
$163,350
Name
Albert Einstein College of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Kunisaki, Yuya; Frenette, Paul S (2014) Influences of vascular niches on hematopoietic stem cell fate. Int J Hematol 99:699-705
Chen, Grace; Zhang, Dachuan; Fuchs, Tobias A et al. (2014) Heme-induced neutrophil extracellular traps contribute to the pathogenesis of sickle cell disease. Blood 123:3818-27
Pinho, Sandra; Lacombe, Julie; Hanoun, Maher et al. (2013) PDGFR* and CD51 mark human nestin+ sphere-forming mesenchymal stem cells capable of hematopoietic progenitor cell expansion. J Exp Med 210:1351-67
Kunisaki, Yuya; Bruns, Ingmar; Scheiermann, Christoph et al. (2013) Arteriolar niches maintain haematopoietic stem cell quiescence. Nature 502:637-43
Frenette, Paul S; Pinho, Sandra; Lucas, Daniel et al. (2013) Mesenchymal stem cell: keystone of the hematopoietic stem cell niche and a stepping-stone for regenerative medicine. Annu Rev Immunol 31:285-316
Bianco, Paolo; Cao, Xu; Frenette, Paul S et al. (2013) The meaning, the sense and the significance: translating the science of mesenchymal stem cells into medicine. Nat Med 19:35-42
Chow, Andrew; Huggins, Matthew; Ahmed, Jalal et al. (2013) CD169ýýý macrophages provide a niche promoting erythropoiesis under homeostasis and stress. Nat Med 19:429-36
Hashimoto, Daigo; Chow, Andrew; Noizat, Clara et al. (2013) Tissue-resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes. Immunity 38:792-804
Scheiermann, Christoph; Kunisaki, Yuya; Frenette, Paul S (2013) Circadian control of the immune system. Nat Rev Immunol 13:190-8
Jang, Jung-Eun; Hidalgo, Andrés; Frenette, Paul S (2012) Intravenous immunoglobulins modulate neutrophil activation and vascular injury through Fc?RIII and SHP-1. Circ Res 110:1057-66

Showing the most recent 10 out of 12 publications