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Cysteine-Rich LIM-Only Protein 4 (CRP4) Promotes Atherogenesis in the ApoE−/− Mouse Model
by
Kuret, Anna
, Lukowski, Robert
, Ruth, Peter
, Adler, Julia
, Längst, Natalie
, Boldt, Karsten
, Peter, Andreas
in
3′,5′-cyclic guanosine monophosphate (cGMP)
/ 3′,5′-cyclic guanosine monophosphate-dependent protein kinase type I (cGKI)
/ Actin
/ acyl-CoA dehydrogenase long chain (ACADL)
/ alpha-Defensins
/ Animals
/ Antioxidants
/ Apolipoprotein E
/ apolipoprotein E (ApoE)
/ Apolipoproteins E
/ Arteriosclerosis
/ Atherogenesis
/ Atherosclerosis
/ Atherosclerosis - metabolism
/ Cell proliferation
/ Cholesterol
/ Coronary vessels
/ Cysteine
/ Cysteine - metabolism
/ cysteine-rich LIM-only protein 4 (CRP4)
/ Diet
/ Disease Models, Animal
/ Experiments
/ Genotype & phenotype
/ High density lipoprotein
/ Kinases
/ Lesions
/ LIM protein
/ Mice
/ microtubule associated monooxygenase
/ Muscle contraction
/ Muscle, Smooth, Vascular - metabolism
/ Myocytes, Smooth Muscle - metabolism
/ Peroxiredoxin
/ Pharmacy
/ Phenotypes
/ Phosphorylation
/ Plaque, Atherosclerotic - pathology
/ Proteins
/ Smooth muscle
/ Transcription
/ Transcription factors
2022
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Cysteine-Rich LIM-Only Protein 4 (CRP4) Promotes Atherogenesis in the ApoE−/− Mouse Model
by
Kuret, Anna
, Lukowski, Robert
, Ruth, Peter
, Adler, Julia
, Längst, Natalie
, Boldt, Karsten
, Peter, Andreas
in
3′,5′-cyclic guanosine monophosphate (cGMP)
/ 3′,5′-cyclic guanosine monophosphate-dependent protein kinase type I (cGKI)
/ Actin
/ acyl-CoA dehydrogenase long chain (ACADL)
/ alpha-Defensins
/ Animals
/ Antioxidants
/ Apolipoprotein E
/ apolipoprotein E (ApoE)
/ Apolipoproteins E
/ Arteriosclerosis
/ Atherogenesis
/ Atherosclerosis
/ Atherosclerosis - metabolism
/ Cell proliferation
/ Cholesterol
/ Coronary vessels
/ Cysteine
/ Cysteine - metabolism
/ cysteine-rich LIM-only protein 4 (CRP4)
/ Diet
/ Disease Models, Animal
/ Experiments
/ Genotype & phenotype
/ High density lipoprotein
/ Kinases
/ Lesions
/ LIM protein
/ Mice
/ microtubule associated monooxygenase
/ Muscle contraction
/ Muscle, Smooth, Vascular - metabolism
/ Myocytes, Smooth Muscle - metabolism
/ Peroxiredoxin
/ Pharmacy
/ Phenotypes
/ Phosphorylation
/ Plaque, Atherosclerotic - pathology
/ Proteins
/ Smooth muscle
/ Transcription
/ Transcription factors
2022
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Cysteine-Rich LIM-Only Protein 4 (CRP4) Promotes Atherogenesis in the ApoE−/− Mouse Model
by
Kuret, Anna
, Lukowski, Robert
, Ruth, Peter
, Adler, Julia
, Längst, Natalie
, Boldt, Karsten
, Peter, Andreas
in
3′,5′-cyclic guanosine monophosphate (cGMP)
/ 3′,5′-cyclic guanosine monophosphate-dependent protein kinase type I (cGKI)
/ Actin
/ acyl-CoA dehydrogenase long chain (ACADL)
/ alpha-Defensins
/ Animals
/ Antioxidants
/ Apolipoprotein E
/ apolipoprotein E (ApoE)
/ Apolipoproteins E
/ Arteriosclerosis
/ Atherogenesis
/ Atherosclerosis
/ Atherosclerosis - metabolism
/ Cell proliferation
/ Cholesterol
/ Coronary vessels
/ Cysteine
/ Cysteine - metabolism
/ cysteine-rich LIM-only protein 4 (CRP4)
/ Diet
/ Disease Models, Animal
/ Experiments
/ Genotype & phenotype
/ High density lipoprotein
/ Kinases
/ Lesions
/ LIM protein
/ Mice
/ microtubule associated monooxygenase
/ Muscle contraction
/ Muscle, Smooth, Vascular - metabolism
/ Myocytes, Smooth Muscle - metabolism
/ Peroxiredoxin
/ Pharmacy
/ Phenotypes
/ Phosphorylation
/ Plaque, Atherosclerotic - pathology
/ Proteins
/ Smooth muscle
/ Transcription
/ Transcription factors
2022
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Cysteine-Rich LIM-Only Protein 4 (CRP4) Promotes Atherogenesis in the ApoE−/− Mouse Model
Journal Article
Cysteine-Rich LIM-Only Protein 4 (CRP4) Promotes Atherogenesis in the ApoE−/− Mouse Model
2022
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Overview
Vascular smooth muscle cells (VSMCs) can switch from their contractile state to a synthetic phenotype resulting in high migratory and proliferative capacity and driving atherosclerotic lesion formation. The cysteine-rich LIM-only protein 4 (CRP4) reportedly modulates VSM-like transcriptional signatures, which are perturbed in VSMCs undergoing phenotypic switching. Thus, we hypothesized that CRP4 contributes to adverse VSMC behaviours and thereby to atherogenesis in vivo. The atherogenic properties of CRP4 were investigated in plaque-prone apolipoprotein E (ApoE) and CRP4 double-knockout (dKO) as well as ApoE-deficient CRP4 wildtype mice. dKO mice exhibited lower plaque numbers and lesion areas as well as a reduced content of α-smooth muscle actin positive cells in the lesion area, while lesion-associated cell proliferation was elevated in vessels lacking CRP4. Reduced plaque volumes in dKO correlated with significantly less intra-plaque oxidized low-density lipoprotein (oxLDL), presumably due to upregulation of the antioxidant factor peroxiredoxin-4 (PRDX4). This study identifies CRP4 as a novel pro-atherogenic factor that facilitates plaque oxLDL deposition and identifies the invasion of atherosclerotic lesions by VSMCs as important determinants of plaque vulnerability. Thus, targeting of VSMC CRP4 should be considered in plaque-stabilizing pharmacological strategies.
Publisher
MDPI AG,MDPI
Subject
3′,5′-cyclic guanosine monophosphate (cGMP)
/ 3′,5′-cyclic guanosine monophosphate-dependent protein kinase type I (cGKI)
/ Actin
/ acyl-CoA dehydrogenase long chain (ACADL)
/ Animals
/ Atherosclerosis - metabolism
/ Cysteine
/ cysteine-rich LIM-only protein 4 (CRP4)
/ Diet
/ Kinases
/ Lesions
/ Mice
/ microtubule associated monooxygenase
/ Muscle, Smooth, Vascular - metabolism
/ Myocytes, Smooth Muscle - metabolism
/ Pharmacy
/ Plaque, Atherosclerotic - pathology
/ Proteins
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