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 in | NeuroImage (Orlando, Fla.) Vol. 28; no. 3; pp. 698 - 707 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Inc
15.11.2005
Elsevier Limited |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1053-8119 1095-9572 |
| DOI | 10.1016/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 |
| Author_xml | – sequence: 1 givenname: Quan surname: Jiang fullname: Jiang, Quan 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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| Keywords | Molecular imaging Angiogenesis Cerebral ischemia Magnetic resonance imaging CBF CBV Permeability |
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| 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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