Investigation of neural progenitor cell induced angiogenesis after embolic stroke in rat using MRI

Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intr...

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Published inNeuroImage (Orlando, Fla.) Vol. 28; no. 3; pp. 698 - 707
Main Authors Jiang, Quan, Zhang, Zheng Gang, Ding, Guang Liang, Zhang, Li, Ewing, James R., Wang, Lei, Zhang, RuiLan, Li, Lian, Lu, Mei, Meng, He, Arbab, Ali S., Hu, Jiani, Li, Qing Jiang, Pourabdollah Nejad D, Siamak, Athiraman, Hemanthkumar, Chopp, Michael
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.11.2005
Elsevier Limited
Subjects
Online AccessGet full text
ISSN1053-8119
1095-9572
DOI10.1016/j.neuroimage.2005.06.063

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Abstract Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke ( n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T 1, T 1sat ( T 1 in the presence of an off-resonance irradiation of the macromolecules of brain), T 2, the inverse of the apparent forward transfer rate for magnetization transfer ( k inv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant ( K i) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K i with a peak at 2 to 3 weeks after cell therapy. Relative T 1, T 1sat, T 2, and k inv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region ( T 1, P < 0.01 at 6 weeks; T 1sat, P < 0.05 at 2 to 6 weeks; T 2, P < 0.05 at 3 to 6 weeks; k inv P < 0.05 at 6 weeks). Of these methods, K i appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T 1sat, T 1, T 2, and k inv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
AbstractList Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T sub(1), T sub(1sat) (T sub(1) in the presence of an off-resonance irradiation of the macromolecules of brain), T sub(2), the inverse of the apparent forward transfer rate for magnetization transfer (k sub(inv)), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (K sub(i)) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P - 0.01; CBV, P - 0.01) at 6 weeks after treatment, and coincident with transient increases of K sub(i) with a peak at 2 to 3 weeks after cell therapy. Relative T sub(1), T sub(1sat), T sub(2), and k sub(inv) decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T sub(1), P - 0.01 at 6 weeks; T sub(1sat), P - 0.05 at 2 to 6 weeks; T sub(2), P - 0.05 at 3 to 6 weeks; k sub(inv) P - 0.05 at 6 weeks). Of these methods, K sub(i) appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T sub(1sat), T sub(1), T sub(2), and k sub(inv) provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T1, T1sat (T1 in the presence of an off-resonance irradiation of the macromolecules of brain), T2, the inverse of the apparent forward transfer rate for magnetization transfer (kinv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (Ki) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K(i) with a peak at 2 to 3 weeks after cell therapy. Relative T1, T1sat, T2, and kinv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T1, P < 0.01 at 6 weeks; T1sat, P < 0.05 at 2 to 6 weeks; T2, P < 0.05 at 3 to 6 weeks; kinvP < 0.05 at 6 weeks). Of these methods, Ki appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T1sat, T1, T2, and kinv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke ( n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T 1, T 1sat ( T 1 in the presence of an off-resonance irradiation of the macromolecules of brain), T 2, the inverse of the apparent forward transfer rate for magnetization transfer ( k inv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant ( K i) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K i with a peak at 2 to 3 weeks after cell therapy. Relative T 1, T 1sat, T 2, and k inv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region ( T 1, P < 0.01 at 6 weeks; T 1sat, P < 0.05 at 2 to 6 weeks; T 2, P < 0.05 at 3 to 6 weeks; k inv P < 0.05 at 6 weeks). Of these methods, K i appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T 1sat, T 1, T 2, and k inv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T1, T1sat (T1 in the presence of an off-resonance irradiation of the macromolecules of brain), T2, the inverse of the apparent forward transfer rate for magnetization transfer (kinv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (Ki) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K(i) with a peak at 2 to 3 weeks after cell therapy. Relative T1, T1sat, T2, and kinv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T1, P < 0.01 at 6 weeks; T1sat, P < 0.05 at 2 to 6 weeks; T2, P < 0.05 at 3 to 6 weeks; kinvP < 0.05 at 6 weeks). Of these methods, Ki appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T1sat, T1, T2, and kinv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T1, T1sat (T1 in the presence of an off-resonance irradiation of the macromolecules of brain), T2, the inverse of the apparent forward transfer rate for magnetization transfer (kinv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (Ki) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K(i) with a peak at 2 to 3 weeks after cell therapy. Relative T1, T1sat, T2, and kinv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T1, P < 0.01 at 6 weeks; T1sat, P < 0.05 at 2 to 6 weeks; T2, P < 0.05 at 3 to 6 weeks; kinvP < 0.05 at 6 weeks). Of these methods, Ki appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T1sat, T1, T2, and kinv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n= 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitativeT1,T1sat(T1in the presence of an off-resonance irradiation of the macromolecules of brain),T2, the inverse of the apparent forward transfer rate for magnetization transfer (kinv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (Ki) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF,P< 0.01; CBV,P< 0.01) at 6 weeks after treatment, and coincident with transient increases ofKiwith a peak at 2 to 3 weeks after cell therapy. RelativeT1,T1sat,T2, andkinvdecreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T1,P< 0.01 at 6 weeks;T1sat,P< 0.05 at 2 to 6 weeks;T2,P< 0.05 at 3 to 6 weeks;kinvP< 0.05 at 6 weeks). Of these methods,Kiappear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV,T1sat,T1,T2, andkinvprovide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
Author Ewing, James R.
Hu, Jiani
Pourabdollah Nejad D, Siamak
Meng, He
Zhang, Li
Zhang, Zheng Gang
Lu, Mei
Athiraman, Hemanthkumar
Jiang, Quan
Ding, Guang Liang
Zhang, RuiLan
Li, Lian
Arbab, Ali S.
Wang, Lei
Li, Qing Jiang
Chopp, Michael
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  surname: Jiang
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  email: quan@neurnis.neuro.hfh.edu
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 2
  givenname: Zheng Gang
  surname: Zhang
  fullname: Zhang, Zheng Gang
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 3
  givenname: Guang Liang
  surname: Ding
  fullname: Ding, Guang Liang
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 4
  givenname: Li
  surname: Zhang
  fullname: Zhang, Li
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 5
  givenname: James R.
  surname: Ewing
  fullname: Ewing, James R.
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 6
  givenname: Lei
  surname: Wang
  fullname: Wang, Lei
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 7
  givenname: RuiLan
  surname: Zhang
  fullname: Zhang, RuiLan
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 8
  givenname: Lian
  surname: Li
  fullname: Li, Lian
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 9
  givenname: Mei
  surname: Lu
  fullname: Lu, Mei
  organization: Department of Biostatistics and Research Epidemiology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 10
  givenname: He
  surname: Meng
  fullname: Meng, He
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 11
  givenname: Ali S.
  surname: Arbab
  fullname: Arbab, Ali S.
  organization: Department of Radiology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 12
  givenname: Jiani
  surname: Hu
  fullname: Hu, Jiani
  organization: Harper Hospital, MR Center, Detroit, MI 48201, USA
– sequence: 13
  givenname: Qing Jiang
  surname: Li
  fullname: Li, Qing Jiang
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 14
  givenname: Siamak
  surname: Pourabdollah Nejad D
  fullname: Pourabdollah Nejad D, Siamak
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 15
  givenname: Hemanthkumar
  surname: Athiraman
  fullname: Athiraman, Hemanthkumar
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
– sequence: 16
  givenname: Michael
  surname: Chopp
  fullname: Chopp, Michael
  organization: Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/16112879$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2005 Elsevier Inc.
Copyright Elsevier Limited Nov 15, 2005
Copyright_xml – notice: 2005 Elsevier Inc.
– notice: Copyright Elsevier Limited Nov 15, 2005
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Magnetic resonance imaging
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Snippet Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic...
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StartPage 698
SubjectTerms Algorithms
Angiogenesis
Animals
Brain - pathology
CBF
CBV
Cells, Cultured
Cerebral ischemia
Cerebrovascular Circulation - physiology
Data Interpretation, Statistical
Echo-Planar Imaging
Epidermal growth factor
Ferrocyanides
Gadolinium
Immunohistochemistry
Intracranial Embolism - complications
Intracranial Embolism - pathology
Ischemia
Lateral Ventricles - pathology
Magnetic Resonance Imaging
Medical imaging
Methods
Molecular imaging
Neovascularization, Physiologic - physiology
Neurons - physiology
Permeability
Rats
Rodents
Stem Cell Transplantation
Stem Cells - physiology
Stereotaxic Techniques
Stroke - etiology
Stroke - pathology
Tomography
Veins & arteries
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Title Investigation of neural progenitor cell induced angiogenesis after embolic stroke in rat using MRI
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