Erythropoietin: Elucidating new cellular targets that broaden therapeutic strategies

被引:121
作者
Maiese, Kenneth [1 ,2 ,3 ,4 ,5 ,6 ]
Chong, Zhao Zhong [3 ]
Li, Faqi [3 ]
Shang, Yan Chen [3 ]
机构
[1] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Anat & Cell Biol, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Div Cellular & Mol Cerebral Ischemia, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[5] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[6] Wayne State Univ, Sch Med, Inst Environm Hlth Sci, Detroit, MI 48201 USA
关键词
Alzheimer's disease; Akt; angiogenesis; apoptosis; cancer; cardiac; caspases; diabetes; endothelial; erythropoietin; forkhead; GSK-3; beta; inflammation; microglia; mitochondria; neurodegeneration; NF-kappa B; renal; STATs; Wnt;
D O I
10.1016/j.pneurobio.2008.02.002
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Given that erythropoietin (EPO) is no longer believed to have exclusive biological activity in the hematopoietic system, EPO is now considered to have applicability in a variety of nervous system disorders that can overlap with vascular disease, metabolic impairments, and immune system function. As a result, EPO may offer efficacy for a broad number of disorders that involve Alzheimer's disease, cardiac insufficiency, stroke, trauma, and diabetic complications. During a number of clinical conditions, EPO is robust and can prevent metabolic compromise, neuronal and vascular degeneration, and inflammatory cell activation. Yet, use of EPO is not without its considerations especially in light of frequent concerns that may compromise clinical care. Recent work has elucidated a number of novel cellular pathways governed by EPO that can open new avenues to avert deleterious effects of this agent and offer previously unrecognized perspectives for therapeutic strategies. Obtaining greater insight into the role of EPO in the nervous system and elucidating its unique cellular pathways may provide greater cellular viability not only in the nervous system but also throughout the body. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:194 / 213
页数:20
相关论文
共 382 条
[1]
ERYTHROPOIETIN HAS A MITOGENIC AND POSITIVE CHEMOTACTIC EFFECT ON ENDOTHELIAL-CELLS [J].
ANAGNOSTOU, A ;
LEE, ES ;
KESSIMIAN, N ;
LEVINSON, R ;
STEINER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5978-5982
[2]
ERYTHROPOIETIN RECEPTOR MESSENGER-RNA EXPRESSION IN HUMAN ENDOTHELIAL-CELLS [J].
ANAGNOSTOU, A ;
LIU, ZY ;
STEINER, M ;
CHIN, K ;
LEE, ES ;
KESSIMIAN, N ;
NOGUCHI, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3974-3978
[3]
[Anonymous], 1855, COMPTES ACAD SCI
[4]
[Anonymous], Z GESANTE EXP MED
[5]
Protective role of endogenous erythropoietin system in nonhematopoietic cells against pressure overload-induced left ventricular dysfunction in mice [J].
Asaumi, Yasuhide ;
Kagaya, Yutaka ;
Takeda, Morihiko ;
Yamaguchi, Nobuhiro ;
Tada, Hiroko ;
Ito, Kenta ;
Ohta, Jun ;
Shiroto, Takashi ;
Shirato, Kunio ;
Minegishi, Naoko ;
Shimokawa, Hiroaki .
CIRCULATION, 2007, 115 (15) :2022-2032
[6]
Erythropoietin stimulates vasculogenesis in neonatal rat mesenteric microvascular endothelial cells [J].
Ashley, RA ;
Dubuque, SH ;
Dvorak, B ;
Woodward, SS ;
Williams, SK ;
Kling, PJ .
PEDIATRIC RESEARCH, 2002, 51 (04) :472-478
[7]
Brain erythropoietin receptor expression in Alzheimer disease and mild cognitive impairment [J].
Assaraf, Michael I. ;
Diaz, Zuanel ;
Liberman, Adrienne ;
Miller, Wilson H., Jr. ;
Arvanitakis, Zoe ;
Li, Yan ;
Bennett, David A. ;
Schipper, Hyman M. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2007, 66 (05) :389-398
[8]
Recombinant erythropoietin down-regulates IL-6 and CXCR4 genes in TNF-α-treated primary cultures of human microvascular endothelial cells -: Implications of multiple sclerosis [J].
Avasarala, JR ;
Konduru, SS .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2005, 25 (02) :183-189
[9]
The relationship between impaired glucose tolerance, type 2 diabetes, and cognitive function [J].
Awad, N ;
Gagnon, M ;
Messier, C .
JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY, 2004, 26 (08) :1044-1080
[10]
Low-dose therapy with the long-acting erythropoietin analogue darbepoetin alpha persistently activates endothelial Akt and attenuates progressive organ failure [J].
Bahlmann, FH ;
Song, R ;
Boehm, SM ;
Mengel, M ;
von Wasielewski, R ;
Lindschau, C ;
Kirsch, T ;
de Groot, K ;
Laudeley, R ;
Niemczyk, E ;
Güler, F ;
Menne, J ;
Haller, H ;
Fliser, D .
CIRCULATION, 2004, 110 (08) :1006-1012