 |
Previous Article | Next Article 
The Journal of Neuroscience, May 15, 1998, 18(10):3699-3707
Upregulation of Pleiotrophin Gene Expression in Developing
Microvasculature, Macrophages, and Astrocytes after Acute Ischemic
Brain Injury
Hsiu-Jeng
Yeh1,
Yong Y.
He2,
Jan
Xu2,
Chung Y.
Hsu2, and
Thomas
F.
Deuel1
1 Department of Medicine, Division of Growth
Regulation, Beth Israel Deaconess Medical Center, Boston, Massachusetts
02215, and 2 Department of Neurology, Washington University
School of Medicine, St. Louis, Missouri 63310
Pleiotrophin (PTN) is a heparin-binding, 18 kDa secretory protein
that functions to induce mitogenesis, angiogenesis, differentiation, and transformation in vitro. PTN gene
(Ptn) expression is highly regulated during development
and is highest at sites in which mitogenesis, angiogenesis, and
differentiation are active. In striking contrast, with the exception of
the neuron, the Ptn gene is only minimally expressed in
adults. We now demonstrate that Ptn gene expression is
strikingly upregulated within 3 d in OX42-positive macrophages, astrocytes, and endothelial cells in areas of developing neovasculature after focal cerebral ischemia in adult rat.
Ptn gene expression remains upregulated in these same
cells and sites 7 and 14 d after ischemic injury. However,
expression of the Ptn gene is significantly decreased in
cortical neurons 6 and 24 hr after injury and is undetectable in
degenerating neurons at day 3. Neurons in contralateral cortex continue
to express Ptn in levels equal to control, uninjured
brain. It is suggested that PTN may have a vital role in neovascular
formation in postischemic brain and that postischemic brain is an
important model in which to analyze sequential gene expression in
developing neovasculature. In contrast, Ptn gene
expression in injured neurons destined not to recover is strikingly
reduced, and potentially its absence may contribute to the failure of
the neuron to survive.
Key words:
pleiotrophin gene expression; ischemia; neovasculature; macrophage; astrocytes
Copyright © 1998 Society for Neuroscience 0270-6474/98/18103699-09$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
Z. Jin, G. Lahat, B. Korchin, T. Nguyen, Q.-S. Zhu, X. Wang, A. J. Lazar, J. Trent, R. E. Pollock, and D. Lev
Midkine Enhances Soft-Tissue Sarcoma Growth: A Possible Novel Therapeutic Target
Clin. Cancer Res.,
August 15, 2008;
14(16):
5033 - 5042.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Li, H. Wei, A. Chesley, C. Moon, M. Krawczyk, M. Volkova, B. Ziman, K. B. Margulies, M. Talan, M. T. Crow, et al.
The Pro-angiogenic Cytokine Pleiotrophin Potentiates Cardiomyocyte Apoptosis through Inhibition of Endogenous AKT/PKB Activity
J. Biol. Chem.,
November 30, 2007;
282(48):
34984 - 34993.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Chen, M. S. Gordon, R. A. Campbell, M. Li, C. S. Wang, H. J. Lee, E. Sanchez, S. J. Manyak, D. Gui, D. Shalitin, et al.
Pleiotrophin is highly expressed by myeloma cells and promotes myeloma tumor growth
Blood,
July 1, 2007;
110(1):
287 - 295.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Mi, W. Chen, and A. Hoke
From the Cover: Pleiotrophin is a neurotrophic factor for spinal motor neurons
PNAS,
March 13, 2007;
104(11):
4664 - 4669.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Li, D. K. Pritchard, X. Wang, D. R. Park, R. E. Bumgarner, S. M. Schwartz, and W. C. Liles
cDNA microarray analysis reveals fundamental differences in the expression profiles of primary human monocytes, monocyte-derived macrophages, and alveolar macrophages
J. Leukoc. Biol.,
January 1, 2007;
81(1):
328 - 335.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. G. Sharifi, Z. Zeng, L. Wang, L. Song, H. Chen, M. Qin, M. R. Sierra-Honigmann, S. Wachsmann-Hogiu, and P. K. Shah
Pleiotrophin Induces Transdifferentiation of Monocytes Into Functional Endothelial Cells
Arterioscler. Thromb. Vasc. Biol.,
June 1, 2006;
26(6):
1273 - 1280.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Pariser, G. Herradon, L. Ezquerra, P. Perez-Pinera, and T. F. Deuel
Pleiotrophin regulates serine phosphorylation and the cellular distribution of {beta}-adducin through activation of protein kinase C
PNAS,
August 30, 2005;
102(35):
12407 - 12412.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Blondet, G. Carpentier, F. Lafdil, and J. Courty
Pleiotrophin Cellular Localization in Nerve Regeneration after Peripheral Nerve Injury
J. Histochem. Cytochem.,
August 1, 2005;
53(8):
971 - 977.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Chen, E. Rubin, H. Zhang, S. Chung, C. C. Jie, E. Garrett, S. Biswal, and S. Sukumar
Identification of Transcriptional Targets of HOXA5
J. Biol. Chem.,
May 13, 2005;
280(19):
19373 - 19380.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
U. Gurok, C. Steinhoff, B. Lipkowitz, H.-H. Ropers, C. Scharff, and U. A. Nuber
Gene Expression Changes in the Course of Neural Progenitor Cell Differentiation
J. Neurosci.,
June 30, 2004;
24(26):
5982 - 6002.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Powers, A. Aigner, G. E. Stoica, K. McDonnell, and A. Wellstein
Pleiotrophin Signaling through Anaplastic Lymphoma Kinase Is Rate-limiting for Glioblastoma Growth
J. Biol. Chem.,
April 12, 2002;
277(16):
14153 - 14158.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J.-i. Satoh and Y. Kuroda
Differing effects of IFN{beta} vs IFN{gamma} in MS: Gene expression in cultured astrocytes
Neurology,
August 28, 2001;
57(4):
681 - 685.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Tokita, H. Keino, F. Matsui, S. Aono, H. Ishiguro, S. Higashiyama, and A. Oohira
Regulation of Neuregulin Expression in the Injured Rat Brain and Cultured Astrocytes
J. Neurosci.,
February 15, 2001;
21(4):
1257 - 1264.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. J. McKeon, M. J. Jurynec, and C. R. Buck
The Chondroitin Sulfate Proteoglycans Neurocan and Phosphacan Are Expressed by Reactive Astrocytes in the Chronic CNS Glial Scar
J. Neurosci.,
December 15, 1999;
19(24):
10778 - 10788.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Zhang, H.-J. Yeh, R. Zhong, Y.-S. Li, and T. F. Deuel
A dominant-negative pleiotrophin mutant introduced by homologous recombination leads to germ-cell apoptosis in male mice
PNAS,
June 8, 1999;
96(12):
6734 - 6738.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. E. Stoica, A. Kuo, A. Aigner, I. Sunitha, B. Souttou, C. Malerczyk, D. J. Caughey, D. Wen, A. Karavanov, A. T. Riegel, et al.
Identification of Anaplastic Lymphoma Kinase as a Receptor for the Growth Factor Pleiotrophin
J. Biol. Chem.,
May 11, 2001;
276(20):
16772 - 16779.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. Meng, A. Rodriguez-Pena, T. Dimitrov, W. Chen, M. Yamin, M. Noda, and T. F. Deuel
Pleiotrophin signals increased tyrosine phosphorylation of beta -catenin through inactivation of the intrinsic catalytic activity of the receptor-type protein tyrosine phosphatase beta /zeta
PNAS,
March 14, 2000;
97(6):
2603 - 2608.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|