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

  • Quan Jiang(corresponding author)
    ,
  • Gang Zhang Zheng
    ,
  • Liang Ding Guang
    ,
  • Li Zhang
    ,
  • James R. Ewing
    ,
  • Lei Wang
*Corresponding author for this work
  • Oakland University
    ,
  • Henry Ford Health System
    ,
  • Harper University Hospital
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

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 T1, T 1sat (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 Ki with a peak at 2 to 3 weeks after cell therapy. Relative T1, T1sat, T2, and k inv 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; kinv P < 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, T 1sat, 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.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 698-707 (10 pages)

Journal (Volume, Issue Number)

NeuroImage (Volume 28, Issue 3)

Publication milestones

  • Published - 11/15/2005

Publication status

Published - 11/15/2005

ISSN

1053-8119

Publication IDs

  • Scopus: 27544488427
  • PubMed: 16112879

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
2.27
SciVal
Author count
16
SciVal
citations
139
SciVal
Paper percentile
96
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.06
Fractional count
15
Fractional count
0.94
Fractional count
1
Fractional count
1

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Citation count
144
Captures
71

Funding Details

This work was supported by NIH grants RO1 NS48349, RO1 NS38292, RO1 NS43324, RO1 HL64766, RO1 HL70023, PO1 NS23393, and PO1 NS42345.