Differential distribution of vasa vasorum in different vascular beds in humans

Heike A. Hildebrandt, Mario Gossl, Dallit Mannheim, Daniele Versari, Joerg Herrmann, Danny Spendlove, Thomas Bajanowski, Nasser M. Malyar, Raimund Erbel, Lilach O Lerman, Amir Lerman

Research output: Contribution to journalArticle

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Abstract

Objective: Vasa vasorum (VV) have been implicated to play a role in the pathogenesis of atherosclerosis. This study was designed to describe the distribution of VV density in different vascular beds in humans and to investigate the association between VV density and the known distribution of atherosclerosis in human arteries. Methods: Forty-two human arteries, harvested at autopsy or after explantation, were analyzed by three-dimensional microscopic-computed tomography (micro-CT). VV density, endothelial-surface-fraction (Σ VV endothelial-surface-area/vessel-wall-volume) and vascular-area-fraction (Σ VV area/vessel-wall-area) were calculated for coronary, renal and femoral arteries. Representatively five coronary, renal and femoral arteries were stained for endothelial cells (von Willebrand-Factor), macrophages (CD68), vascular endothelial growth factor (VEGF) and collagen (Sirius Red). Results: Coronary arteries showed a higher VV density compared to renal and femoral arteries (2.12 ± 0.26 n/mm2 versus 0.61 ± 0.06 n/mm2 and 0.66 ± 0.11 n/mm2; P < 0.05 for both) as well as a higher endothelial-surface-fraction and vascular-area-fraction. Histology showed a positive correlation between histologically derived VV density and CD68-positive cells/area (r = 0.54, P < 0.01), VEGF-immunoreactivity/area (r = 0.55, P < 0.01) and a negative correlation between VV density and collagen I content (r = 0.66, P < 0.05). Conclusion: This micro-CT study highlights a higher VV density in coronary than in peripheral arteries, supporting the relation between VV density and the susceptibility to atherosclerosis in different vascular beds in humans.

Original languageEnglish (US)
Pages (from-to)47-54
Number of pages8
JournalAtherosclerosis
Volume199
Issue number1
DOIs
StatePublished - Jul 2008

Fingerprint

Vasa Vasorum
Blood Vessels
Renal Artery
Femoral Artery
Atherosclerosis
Coronary Vessels
Arteries
Vascular Endothelial Growth Factor A
Collagen
Tomography
von Willebrand Factor
Autopsy
Histology

Keywords

  • Atherosclerosis
  • Human
  • Micro-CT
  • Vasa vasorum

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Differential distribution of vasa vasorum in different vascular beds in humans. / Hildebrandt, Heike A.; Gossl, Mario; Mannheim, Dallit; Versari, Daniele; Herrmann, Joerg; Spendlove, Danny; Bajanowski, Thomas; Malyar, Nasser M.; Erbel, Raimund; Lerman, Lilach O; Lerman, Amir.

In: Atherosclerosis, Vol. 199, No. 1, 07.2008, p. 47-54.

Research output: Contribution to journalArticle

Hildebrandt, HA, Gossl, M, Mannheim, D, Versari, D, Herrmann, J, Spendlove, D, Bajanowski, T, Malyar, NM, Erbel, R, Lerman, LO & Lerman, A 2008, 'Differential distribution of vasa vasorum in different vascular beds in humans', Atherosclerosis, vol. 199, no. 1, pp. 47-54. https://doi.org/10.1016/j.atherosclerosis.2007.09.015
Hildebrandt, Heike A. ; Gossl, Mario ; Mannheim, Dallit ; Versari, Daniele ; Herrmann, Joerg ; Spendlove, Danny ; Bajanowski, Thomas ; Malyar, Nasser M. ; Erbel, Raimund ; Lerman, Lilach O ; Lerman, Amir. / Differential distribution of vasa vasorum in different vascular beds in humans. In: Atherosclerosis. 2008 ; Vol. 199, No. 1. pp. 47-54.
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abstract = "Objective: Vasa vasorum (VV) have been implicated to play a role in the pathogenesis of atherosclerosis. This study was designed to describe the distribution of VV density in different vascular beds in humans and to investigate the association between VV density and the known distribution of atherosclerosis in human arteries. Methods: Forty-two human arteries, harvested at autopsy or after explantation, were analyzed by three-dimensional microscopic-computed tomography (micro-CT). VV density, endothelial-surface-fraction (Σ VV endothelial-surface-area/vessel-wall-volume) and vascular-area-fraction (Σ VV area/vessel-wall-area) were calculated for coronary, renal and femoral arteries. Representatively five coronary, renal and femoral arteries were stained for endothelial cells (von Willebrand-Factor), macrophages (CD68), vascular endothelial growth factor (VEGF) and collagen (Sirius Red). Results: Coronary arteries showed a higher VV density compared to renal and femoral arteries (2.12 ± 0.26 n/mm2 versus 0.61 ± 0.06 n/mm2 and 0.66 ± 0.11 n/mm2; P < 0.05 for both) as well as a higher endothelial-surface-fraction and vascular-area-fraction. Histology showed a positive correlation between histologically derived VV density and CD68-positive cells/area (r = 0.54, P < 0.01), VEGF-immunoreactivity/area (r = 0.55, P < 0.01) and a negative correlation between VV density and collagen I content (r = 0.66, P < 0.05). Conclusion: This micro-CT study highlights a higher VV density in coronary than in peripheral arteries, supporting the relation between VV density and the susceptibility to atherosclerosis in different vascular beds in humans.",
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AU - Hildebrandt, Heike A.

AU - Gossl, Mario

AU - Mannheim, Dallit

AU - Versari, Daniele

AU - Herrmann, Joerg

AU - Spendlove, Danny

AU - Bajanowski, Thomas

AU - Malyar, Nasser M.

AU - Erbel, Raimund

AU - Lerman, Lilach O

AU - Lerman, Amir

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N2 - Objective: Vasa vasorum (VV) have been implicated to play a role in the pathogenesis of atherosclerosis. This study was designed to describe the distribution of VV density in different vascular beds in humans and to investigate the association between VV density and the known distribution of atherosclerosis in human arteries. Methods: Forty-two human arteries, harvested at autopsy or after explantation, were analyzed by three-dimensional microscopic-computed tomography (micro-CT). VV density, endothelial-surface-fraction (Σ VV endothelial-surface-area/vessel-wall-volume) and vascular-area-fraction (Σ VV area/vessel-wall-area) were calculated for coronary, renal and femoral arteries. Representatively five coronary, renal and femoral arteries were stained for endothelial cells (von Willebrand-Factor), macrophages (CD68), vascular endothelial growth factor (VEGF) and collagen (Sirius Red). Results: Coronary arteries showed a higher VV density compared to renal and femoral arteries (2.12 ± 0.26 n/mm2 versus 0.61 ± 0.06 n/mm2 and 0.66 ± 0.11 n/mm2; P < 0.05 for both) as well as a higher endothelial-surface-fraction and vascular-area-fraction. Histology showed a positive correlation between histologically derived VV density and CD68-positive cells/area (r = 0.54, P < 0.01), VEGF-immunoreactivity/area (r = 0.55, P < 0.01) and a negative correlation between VV density and collagen I content (r = 0.66, P < 0.05). Conclusion: This micro-CT study highlights a higher VV density in coronary than in peripheral arteries, supporting the relation between VV density and the susceptibility to atherosclerosis in different vascular beds in humans.

AB - Objective: Vasa vasorum (VV) have been implicated to play a role in the pathogenesis of atherosclerosis. This study was designed to describe the distribution of VV density in different vascular beds in humans and to investigate the association between VV density and the known distribution of atherosclerosis in human arteries. Methods: Forty-two human arteries, harvested at autopsy or after explantation, were analyzed by three-dimensional microscopic-computed tomography (micro-CT). VV density, endothelial-surface-fraction (Σ VV endothelial-surface-area/vessel-wall-volume) and vascular-area-fraction (Σ VV area/vessel-wall-area) were calculated for coronary, renal and femoral arteries. Representatively five coronary, renal and femoral arteries were stained for endothelial cells (von Willebrand-Factor), macrophages (CD68), vascular endothelial growth factor (VEGF) and collagen (Sirius Red). Results: Coronary arteries showed a higher VV density compared to renal and femoral arteries (2.12 ± 0.26 n/mm2 versus 0.61 ± 0.06 n/mm2 and 0.66 ± 0.11 n/mm2; P < 0.05 for both) as well as a higher endothelial-surface-fraction and vascular-area-fraction. Histology showed a positive correlation between histologically derived VV density and CD68-positive cells/area (r = 0.54, P < 0.01), VEGF-immunoreactivity/area (r = 0.55, P < 0.01) and a negative correlation between VV density and collagen I content (r = 0.66, P < 0.05). Conclusion: This micro-CT study highlights a higher VV density in coronary than in peripheral arteries, supporting the relation between VV density and the susceptibility to atherosclerosis in different vascular beds in humans.

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