scholarly journals Characterization of hepatic macrophages and evaluation of inflammatory response in heme oxygenase-1 deficient mice exposed to scAAV9 vectors

PLoS ONE ◽  
2020 ◽  
Vol 15 (10) ◽  
pp. e0240691
Author(s):  
Mateusz Tomczyk ◽  
Izabela Kraszewska ◽  
Robert Mąka ◽  
Agnieszka Waligórska ◽  
Józef Dulak ◽  
...  
Keyword(s):  
Inflammatory Response ◽  
Heme Oxygenase ◽  
Heme Oxygenase 1 ◽  
Hepatic Macrophages ◽  
Deficient Mice

scholarly journals 323: Pravastatin improves pregnancy outcome and placental development in heme oxygenase-1 deficient mice

2018 ◽  
Vol 218 (1) ◽  
pp. S202-S203
Author(s):  
Abraham Tsur ◽  
Flora Kalish ◽  
Jordan Burgess ◽  
Hui Zhao ◽  
Kerriann Casey ◽  
...  
Keyword(s):  
Pregnancy Outcome ◽  
Heme Oxygenase ◽  
Heme Oxygenase 1 ◽  
Placental Development ◽  
Deficient Mice

scholarly journals Splenic Ly6Chi monocytes contribute to adverse late post-ischemic left ventricular remodeling in heme oxygenase-1 deficient mice

2017 ◽  
Vol 112 (4) ◽  
Author(s):  
Mateusz Tomczyk ◽  
Izabela Kraszewska ◽  
Krzysztof Szade ◽  
Karolina Bukowska-Strakova ◽  
Marco Meloni ◽  
...  
Keyword(s):  
Heme Oxygenase ◽  
Ventricular Remodeling ◽  
Left Ventricular Remodeling ◽  
Left Ventricular ◽  
Heme Oxygenase 1 ◽  
Deficient Mice

Nobiletin Attenuates the Inflammatory Response Through Heme Oxygenase-1 Induction in the Crosstalk Between Adipocytes and Macrophages

2017 ◽  
Vol 20 (9) ◽  
pp. 873-881 ◽  
Author(s):  
Seulgi Namkoong ◽  
Jeehye Sung ◽  
Jinwoo Yang ◽  
Youngmin Choi ◽  
Heon Sang Jeong ◽  
...  
Keyword(s):  
Inflammatory Response ◽  
Heme Oxygenase ◽  
Heme Oxygenase 1

Abstract 18540: Heme Oxygenase 1 Activity and Expression Suppresses a Proinflammatory Phenotype in Monocytes and Correlates With Endothelial Function in Mice and Humans

Circulation ◽  
2014 ◽  
Vol 130 (suppl_2) ◽  
Author(s):  
Philip Wenzel ◽  
Heidi Rossmann ◽  
Christian Müller ◽  
Sabine Kossmann ◽  
Canan Simsek ◽  
...  
Keyword(s):  
Nadph Oxidase ◽  
Arterial Hypertension ◽  
Heme Oxygenase ◽  
Vascular Function ◽  
Vascular Dysfunction ◽  
Isometric Tension ◽  
Health Study ◽  
Heme Oxygenase 1 ◽  
Frequency Pattern ◽  
Deficient Mice

Background: Heme oxygenase-1 (HO-1) confers protection to the vasculature and suppresses inflammatory properties of monocytes and macrophages. It is unclear how HO-1 activity and expression determine the extent of vascular dysfunction in mice and humans. Methods and results: Decreasing HO activity was parallelled by decreasing aortic HO-1, eNOS and phospho-eNOS (ser1177) protein expression in HO-1 deficient mice, whereas aortic expression of nox2 showed a stepwise increase in HO-1+/- and HO-1-/- mice as compared to HO-1+/+ controls. Aortic superoxide formation increased depending on the extent of HO-1 deficiency and was blunted by the PKC inhibitor chelerythrine, indicating activation of the NADPH oxidase. When subjected to disease models of vascular dysfunction - angiotensin II-infusion (ATII, 0.1mg/kg/d for 7d), streptozotocin-induced diabetes mellitus and aging - HO-1 deficient mice showed an increased vascular dysfunction (shown by isometric tension studies) that was inversely correlated with HO activity. In a primary prevention population based cohort (the Gutenberg Health Study, GHS), we assessed length polymorphisms of the HO-1 promoter region, established a bipolar frequency pattern of allele length (long vs short repeats) in 4937 individuals and found a moderately significant association with flow mediated dilation of the brachial artery (FMD) in individuals with arterial hypertension. Monocytic HO-1 mRNA expression was positively correlated with CD14 expression indicating proinflammatory monocytes (p<0.001) and inversely with FMD in 733 hypertensive individuals of the GHS. ATII-infused HO-1+/+ mice had a significant infiltration of proinflammatory CD11b+Ly6Chi monocytes into the aortic wall, which was sharpely increased in HO-1+/- and HO-1-/- mice, providing a mechanistic link of the monocyte phenotype determined by HO-1 and vascular dysfunction in arterial hypertension. Conclusions: We here present evidence that HO activity and expression and inversely correlates with vascular dysfunction and NADPH oxidase mediated oxidative stress in mice and humans. We conclude, that HO-1 is a regulator of vascular function in hypertension via determining the phenotype of inflammatory circulating and infiltrating monocytes.

scholarly journals Exacerbation of Neonatal Hemolysis and Impaired Renal Iron Handling in Heme Oxygenase 1-Deficient Mice

2020 ◽  
Vol 21 (20) ◽  
pp. 7754
Author(s):  
Aleksandra Bednarz ◽  
Paweł Lipiński ◽  
Rafał R. Starzyński ◽  
Mateusz Tomczyk ◽  
Izabela Kraszewska ◽  
...  
Keyword(s):  
Heme Oxygenase ◽  
Neonatal Period ◽  
Transient State ◽  
The Body ◽  
Heme Oxygenase 1 ◽  
Iron Species ◽  
Renal Epithelium ◽  
Molecular Machinery ◽  
Iron Retention ◽  
Deficient Mice

In most mammals, neonatal intravascular hemolysis is a benign and moderate disorder that usually does not lead to anemia. During the neonatal period, kidneys play a key role in detoxification and recirculation of iron species released from red blood cells (RBC) and filtered out by glomeruli to the primary urine. Activity of heme oxygenase 1 (HO1), a heme-degrading enzyme localized in epithelial cells of proximal tubules, seems to be of critical importance for both processes. We show that, in HO1 knockout mouse newborns, hemolysis was prolonged despite a transient state and exacerbated, which led to temporal deterioration of RBC status. In neonates lacking HO1, functioning of renal molecular machinery responsible for iron reabsorption from the primary urine (megalin/cubilin complex) and its transfer to the blood (ferroportin) was either shifted in time or impaired, respectively. Those abnormalities resulted in iron loss from the body (excreted in urine) and in iron retention in the renal epithelium. We postulate that, as a consequence of these abnormalities, a tight systemic iron balance of HO1 knockout neonates may be temporarily affected.

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