Nutritional B vitamin deficiency alters the expression of key proteins associated with vascular smooth muscle cell proliferation and migration in the aorta of atherosclerotic apolipoprotein E null mice

Susan J Duthie, John H Beattie, Margaret-J Gordon, Lynn P Pirie, Fergus Nicol, Martin D Reid, Gary J Duncan, Louise Cantlay, Graham Horgan, Christopher J McNeil

Research output: Contribution to journalArticle

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Abstract

Low B vitamin status is linked with human vascular disease. We employed a proteomic and biochemical approach to determine whether nutritional folate deficiency and/or hyperhomocysteinemia altered metabolic processes linked with atherosclerosis in ApoE null mice. Animals were fed either a control fat (C; 4 % w/w lard) or a high-fat [HF; 21 % w/w lard and cholesterol (0/15 % w/w)] diet with different B vitamin compositions for 16 weeks. Aorta tissue was prepared and global protein expression, B vitamin, homocysteine and lipoprotein status measured. Changes in the expression of aorta proteins were detected in response to multiple B vitamin deficiency combined with a high-fat diet (P < 0.05) and were strongly linked with lipoprotein concentrations measured directly in the aorta adventitia (P < 0.001). Pathway analysis revealed treatment effects in the aorta-related primarily to cytoskeletal organisation, smooth muscle cell adhesion and invasiveness (e.g., fibrinogen, moesin, transgelin, vimentin). Combined B vitamin deficiency induced striking quantitative changes in the expression of aorta proteins in atherosclerotic ApoE null mice. Deregulated expression of these proteins is associated with human atherosclerosis. Cellular pathways altered by B vitamin status included cytoskeletal organisation, cell differentiation and migration, oxidative stress and chronic inflammation. These findings provide new insight into the molecular mechanisms through which B vitamin deficiency may accelerate atherosclerosis.

Original languageEnglish
Article number446
Number of pages11
JournalGenes & Nutrition
Volume10
Issue number1
Early online date2 Dec 2014
DOIs
Publication statusPublished - Jan 2015

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Vitamin B Deficiency
Apolipoproteins E
Vitamin B Complex
Vascular Smooth Muscle
Smooth Muscle Myocytes
Cell Movement
Aorta
Cell Proliferation
Atherosclerosis
Proteins
Lipoproteins
Fats
Adventitia
Hyperhomocysteinemia
High Fat Diet
Homocysteine
Vimentin
Vascular Diseases
Folic Acid
Cell Adhesion

Keywords

  • aorta proteome
  • ApoE null mice
  • atherosclerosis
  • B vitamins
  • hyperhomocysteinemia

Cite this

Nutritional B vitamin deficiency alters the expression of key proteins associated with vascular smooth muscle cell proliferation and migration in the aorta of atherosclerotic apolipoprotein E null mice. / Duthie, Susan J; Beattie, John H; Gordon, Margaret-J; Pirie, Lynn P; Nicol, Fergus; Reid, Martin D; Duncan, Gary J; Cantlay, Louise; Horgan, Graham; McNeil, Christopher J.

In: Genes & Nutrition, Vol. 10, No. 1, 446, 01.2015.

Research output: Contribution to journalArticle

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abstract = "Low B vitamin status is linked with human vascular disease. We employed a proteomic and biochemical approach to determine whether nutritional folate deficiency and/or hyperhomocysteinemia altered metabolic processes linked with atherosclerosis in ApoE null mice. Animals were fed either a control fat (C; 4 {\%} w/w lard) or a high-fat [HF; 21 {\%} w/w lard and cholesterol (0/15 {\%} w/w)] diet with different B vitamin compositions for 16 weeks. Aorta tissue was prepared and global protein expression, B vitamin, homocysteine and lipoprotein status measured. Changes in the expression of aorta proteins were detected in response to multiple B vitamin deficiency combined with a high-fat diet (P < 0.05) and were strongly linked with lipoprotein concentrations measured directly in the aorta adventitia (P < 0.001). Pathway analysis revealed treatment effects in the aorta-related primarily to cytoskeletal organisation, smooth muscle cell adhesion and invasiveness (e.g., fibrinogen, moesin, transgelin, vimentin). Combined B vitamin deficiency induced striking quantitative changes in the expression of aorta proteins in atherosclerotic ApoE null mice. Deregulated expression of these proteins is associated with human atherosclerosis. Cellular pathways altered by B vitamin status included cytoskeletal organisation, cell differentiation and migration, oxidative stress and chronic inflammation. These findings provide new insight into the molecular mechanisms through which B vitamin deficiency may accelerate atherosclerosis.",
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AU - Cantlay, Louise

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