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Public release date: 1-Feb-2013[ | E-mail |
Share ] Contact: Jillian Hurst
press_releases@the-jci.org
Journal of Clinical Investigation
A gut feeling about neural stem cells
Proper function of the digestive system requires coordinated contraction of the muscle in the wall of the intestinal tract, regulated by the enteric nervous system. Damage or loss of these neurons can result in intestinal motility disorders, such as Hirschsprung's disease, for which there is a dearth of effective treatments. In principle, disorders of the enteric nervous system could be treated by cell therapy, but it was previously unknown whether transplanted stem cells could migrate to the appropriate location in the gut and then become neurons that could properly innervate the bowel. In this issue of the Journal of Clinical Investigation, Heather Young and colleagues at the University of Melbourne, isolated neural stem cells from mice, cultured them to promote the formation of neural precursor cells, and implanted them into the muscle in the colons of recipient mice. Young and colleagues found that these cells were able to migrate away from the transplantation site and develop into neurons that provided stimulation to the portions of the gut the regulate motility. These findings suggest that the transplantation of neural stem cells is a promising therapeutic avenue for the treatment of gastrointestinal motility disorders.
TITLE:
Transplanted progenitors generate functional enteric neurons in the postnatal colon
AUTHOR CONTACT:
Heather Young
University of Melbourne, Parkville, UNK, AUS
Phone: +61383440007; E-mail: h.young@unimelb.edu.au
View this article at: http://www.jci.org/articles/view/65963?key=022ab1c35b2caee56d0e
A cellular adhesion protein protects against inflammation
Cellular inflammation is mediated by a group of proteins known as the inflammasome. In this issue of the Journal of Clinical Investigation, Ziad Mallat and colleagues at Addenbrooke's Hospital in Cambridge, England, identified a protein, MFGE8, that blocks inflammasome activity. Using a mouse model of stroke, Mallat and colleagues determined that expression of MFGE8 inhibited the production of pro-inflammatory products and limited the area of injury after stroke. These results identify MFGE8 as an important regulator of inflammation that could potentially serve as a useful therapeutic target in inflammatory disease.
TITLE:
MFGE8 inhibits inflammasome-induced IL-1? production and limits post-ischemic cerebral injury
AUTHOR CONTACT:
Ziad Mallat
University of Cambridge, Cambridge, GBR
Phone: +44 (0)1223 746720; E-mail: zm255@medschl.cam.ac.uk
View this article at: http://www.jci.org/articles/view/65167?key=9c368b2173b91a4a0e01
ALSO IN THIS ISSUE
TITLE:
IQGAP1 suppresses T?RII-mediated myofibroblastic activation and metastatic growth in liver
AUTHOR CONTACT:
Ningling Kang
Mayo Clinic in Rochester, Rochester, MN, USA
Phone: 5075387552; E-mail: kang.ningling@mayo.edu
View this article at: http://www.jci.org/articles/view/64742?key=5c508faefc60a69bb7a1
TITLE:
Virus-induced hepatocellular carcinomas cause antigen-specific local tolerance
AUTHOR CONTACT:
Thomas Blankenstein
Max Delbrck Center for Molecular Medicine, Berlin, DEU
Phone: 49-30-9406-2816; Fax: 49-30-9406-2453; E-mail: tblanke@mdc-berlin.de
View this article at: http://www.jci.org/articles/view/64742?key=5c508faefc60a69bb7a1
TITLE:
Host immunity contributes to the anti-melanoma activity of BRAF inhibitors
AUTHOR CONTACT:
Mark J. Smyth
Peter MacCallum Cancer Institute, Victoria, AUS
Phone: 61 3 96563728; Fax: 61 3 92561411; E-mail: Mark.Smyth@petermac.org
View this article at: http://www.jci.org/articles/view/66236?key=b2940314699742354322
TITLE:
Adeno-associated virus capsid antigen presentation is dependent on endosomal escape
AUTHOR CONTACT:
R. Jude Samulski
The Gene Therapy Center, Chapel Hill, NC, USA
Phone: 919.962.3285; Fax: 919-966-0907; E-mail: rjs@med.unc.edu
View this article at: http://www.jci.org/articles/view/66611?key=2230ec7324c7af802573
TITLE:
Two-photon imaging of phagocyte-mediated T cell activation in the CNS
AUTHOR CONTACT:
Naoto Kawakami
*Ludwig Maximilians Universitt Mnchen, Institute of Clinical Neuroimmunol, Munich, DEU
Phone: +49 89 7095 8386; Fax: +49 89 7095 8380; E-mail: Naoto.Kawakami@med.uni-muenchen.de
View this article at: http://www.jci.org/articles/view/67233?key=e9bf7e5b2d653d95812f
TITLE:
p53 centrosomal localization diagnoses ataxia-telangiectasia homozygotes and heterozygotes
AUTHOR CONTACT:
Silvia Soddu
Regina Elena Cancer Institute, Rome, ITA
Phone: +39 065266 2492; Fax: +39 065266 2505; E-mail:soddu@ifo.it
View this article at: http://www.jci.org/articles/view/67289?key=e370c09cca244ec50c53>http://www.jci.org/articles/view/67289?key=e370c09cca244ec50c53
###
[ | E-mail | Share ] ?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Public release date: 1-Feb-2013[ | E-mail |
Share ] Contact: Jillian Hurst
press_releases@the-jci.org
Journal of Clinical Investigation
A gut feeling about neural stem cells
Proper function of the digestive system requires coordinated contraction of the muscle in the wall of the intestinal tract, regulated by the enteric nervous system. Damage or loss of these neurons can result in intestinal motility disorders, such as Hirschsprung's disease, for which there is a dearth of effective treatments. In principle, disorders of the enteric nervous system could be treated by cell therapy, but it was previously unknown whether transplanted stem cells could migrate to the appropriate location in the gut and then become neurons that could properly innervate the bowel. In this issue of the Journal of Clinical Investigation, Heather Young and colleagues at the University of Melbourne, isolated neural stem cells from mice, cultured them to promote the formation of neural precursor cells, and implanted them into the muscle in the colons of recipient mice. Young and colleagues found that these cells were able to migrate away from the transplantation site and develop into neurons that provided stimulation to the portions of the gut the regulate motility. These findings suggest that the transplantation of neural stem cells is a promising therapeutic avenue for the treatment of gastrointestinal motility disorders.
TITLE:
Transplanted progenitors generate functional enteric neurons in the postnatal colon
AUTHOR CONTACT:
Heather Young
University of Melbourne, Parkville, UNK, AUS
Phone: +61383440007; E-mail: h.young@unimelb.edu.au
View this article at: http://www.jci.org/articles/view/65963?key=022ab1c35b2caee56d0e
A cellular adhesion protein protects against inflammation
Cellular inflammation is mediated by a group of proteins known as the inflammasome. In this issue of the Journal of Clinical Investigation, Ziad Mallat and colleagues at Addenbrooke's Hospital in Cambridge, England, identified a protein, MFGE8, that blocks inflammasome activity. Using a mouse model of stroke, Mallat and colleagues determined that expression of MFGE8 inhibited the production of pro-inflammatory products and limited the area of injury after stroke. These results identify MFGE8 as an important regulator of inflammation that could potentially serve as a useful therapeutic target in inflammatory disease.
TITLE:
MFGE8 inhibits inflammasome-induced IL-1? production and limits post-ischemic cerebral injury
AUTHOR CONTACT:
Ziad Mallat
University of Cambridge, Cambridge, GBR
Phone: +44 (0)1223 746720; E-mail: zm255@medschl.cam.ac.uk
View this article at: http://www.jci.org/articles/view/65167?key=9c368b2173b91a4a0e01
ALSO IN THIS ISSUE
TITLE:
IQGAP1 suppresses T?RII-mediated myofibroblastic activation and metastatic growth in liver
AUTHOR CONTACT:
Ningling Kang
Mayo Clinic in Rochester, Rochester, MN, USA
Phone: 5075387552; E-mail: kang.ningling@mayo.edu
View this article at: http://www.jci.org/articles/view/64742?key=5c508faefc60a69bb7a1
TITLE:
Virus-induced hepatocellular carcinomas cause antigen-specific local tolerance
AUTHOR CONTACT:
Thomas Blankenstein
Max Delbrck Center for Molecular Medicine, Berlin, DEU
Phone: 49-30-9406-2816; Fax: 49-30-9406-2453; E-mail: tblanke@mdc-berlin.de
View this article at: http://www.jci.org/articles/view/64742?key=5c508faefc60a69bb7a1
TITLE:
Host immunity contributes to the anti-melanoma activity of BRAF inhibitors
AUTHOR CONTACT:
Mark J. Smyth
Peter MacCallum Cancer Institute, Victoria, AUS
Phone: 61 3 96563728; Fax: 61 3 92561411; E-mail: Mark.Smyth@petermac.org
View this article at: http://www.jci.org/articles/view/66236?key=b2940314699742354322
TITLE:
Adeno-associated virus capsid antigen presentation is dependent on endosomal escape
AUTHOR CONTACT:
R. Jude Samulski
The Gene Therapy Center, Chapel Hill, NC, USA
Phone: 919.962.3285; Fax: 919-966-0907; E-mail: rjs@med.unc.edu
View this article at: http://www.jci.org/articles/view/66611?key=2230ec7324c7af802573
TITLE:
Two-photon imaging of phagocyte-mediated T cell activation in the CNS
AUTHOR CONTACT:
Naoto Kawakami
*Ludwig Maximilians Universitt Mnchen, Institute of Clinical Neuroimmunol, Munich, DEU
Phone: +49 89 7095 8386; Fax: +49 89 7095 8380; E-mail: Naoto.Kawakami@med.uni-muenchen.de
View this article at: http://www.jci.org/articles/view/67233?key=e9bf7e5b2d653d95812f
TITLE:
p53 centrosomal localization diagnoses ataxia-telangiectasia homozygotes and heterozygotes
AUTHOR CONTACT:
Silvia Soddu
Regina Elena Cancer Institute, Rome, ITA
Phone: +39 065266 2492; Fax: +39 065266 2505; E-mail:soddu@ifo.it
View this article at: http://www.jci.org/articles/view/67289?key=e370c09cca244ec50c53>http://www.jci.org/articles/view/67289?key=e370c09cca244ec50c53
###
[ | E-mail | Share ] ?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Source: http://www.eurekalert.org/pub_releases/2013-02/joci-jet012513.php
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