Literature DB >> 12767717

Protein transduction technology offers novel therapeutic approach for brain ischemia.

Catherine Denicourt1, Steven F Dowdy.   

Abstract

Transient or permanent reduction in cerebral blood flow following ischemia can lead to severe and irreversible tissue damage to the brain. Emerging biochemical evidence suggests a role for apoptosis in neuronal death following cerebral ischemia. Despite the abundance of studies on the subject, therapeutic interventions for ischemia-related cell injury have so far proved disappointing in clinical trials. Recently, four new, exciting studies reported the use of protein transduction technology to deliver anti-apoptotic molecules to protect neuronal cells following ischemic stroke in vivo. These studies offer new avenues for the treatment and prevention of cell death following brain injuries.

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Year:  2003        PMID: 12767717     DOI: 10.1016/S0165-6147(03)00074-9

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  16 in total

1.  TAT-mediated protein transduction of Nogo extracellular peptide 1-40 and its biological activity.

Authors:  Qiang Wang; Xingchun Gou; Weilin Jin; Lize Xiong; Lichao Hou; Shaoyang Chen; Hui Zhang; Xiaoling Zhu; Lixian Xu
Journal:  Cell Mol Neurobiol       Date:  2008-08-29       Impact factor: 5.046

Review 2.  Gene activation and protein expression following ischaemic stroke: strategies towards neuroprotection.

Authors:  M Slevin; J Krupinski; P Kumar; J Gaffney; S Kumar
Journal:  J Cell Mol Med       Date:  2005 Jan-Mar       Impact factor: 5.310

3.  Tat-Mediated Peptide Intervention in Analgesia and Anesthesia.

Authors:  Feng Tao; Roger A Johns
Journal:  Drug Dev Res       Date:  2010-04-01       Impact factor: 4.360

4.  Inhibition of Epstein-Barr virus-induced growth proliferation by a nuclear antigen EBNA2-TAT peptide.

Authors:  Christopher J Farrell; Jae Myun Lee; Eui-Cheol Shin; Marek Cebrat; Philip A Cole; S Diane Hayward
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-19       Impact factor: 11.205

5.  Cell-permeable peptide Tat-PSD-95 PDZ2 inhibits chronic inflammatory pain behaviors in mice.

Authors:  Feng Tao; Qingning Su; Roger A Johns
Journal:  Mol Ther       Date:  2008-09-09       Impact factor: 11.454

6.  Single-cell imaging of retinal ganglion cell apoptosis with a cell-penetrating, activatable peptide probe in an in vivo glaucoma model.

Authors:  Edward M Barnett; Xu Zhang; Dustin Maxwell; Qing Chang; David Piwnica-Worms
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-20       Impact factor: 11.205

7.  TAT-mediated intracellular delivery of NPM-derived peptide induces apoptosis in leukemic cells and suppresses leukemogenesis in mice.

Authors:  Yun Zhou; Wei Du; Tara Koretsky; Grover C Bagby; Qishen Pang
Journal:  Blood       Date:  2008-06-23       Impact factor: 22.113

8.  Pathway for polyarginine entry into mammalian cells.

Authors:  Stephen M Fuchs; Ronald T Raines
Journal:  Biochemistry       Date:  2004-03-09       Impact factor: 3.162

9.  Effect of disrupting N-methyl-d-aspartate receptor-postsynaptic density protein-95 interactions on the threshold for halothane anesthesia in mice.

Authors:  Feng Tao; Roger A Johns
Journal:  Anesthesiology       Date:  2008-05       Impact factor: 7.892

10.  Heme Oxygenase-1 Protects Neurons from Ischemic Damage by Upregulating Expression of Cu,Zn-Superoxide Dismutase, Catalase, and Brain-Derived Neurotrophic Factor in the Rabbit Spinal Cord.

Authors:  Hyo Young Jung; Dae Won Kim; Hee Sun Yim; Dae Young Yoo; Jong Whi Kim; Moo-Ho Won; Yeo Sung Yoon; Soo Young Choi; In Koo Hwang
Journal:  Neurochem Res       Date:  2015-11-11       Impact factor: 3.996

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