[InlineMediaObject not available: see fulltext.] In focus in HCB

[InlineMediaObject not available: see fulltext.] In focus in HCB Histochem Cell Biol (2017) 148:217–218 DOI 10.1007/s00418-017-1598-9 EDITORIAL In focus in HCB 1 2 Douglas J. Taatjes  · Jürgen Roth   Accepted: 12 July 2017 / Published online: 19 July 2017 © Springer-Verlag GmbH Germany 2017 New system for monitoring brain neuronal activity thus offers a novel means to monitor and image fluores - cently labeled neurons in deep regions of an awake and in moving rats active rat. One of the great challenges in live animal imaging is the accurate recording of brain neuronal activity in a free-mov- Rotenone effect on peroxisomal dynamics ing animal. Although multiphoton confocal microscopy has been used successfully to image more peripheral regions mediated by microtubules of the brain (Kerr et al. 2005), deeper regions remain inac- cessible. Iijima et al. (2017) have now developed a system Redox biology is an area of great interest for cell biologi- cal responses in health and disease (Little et al. 2017). Two consisting of (1) a single optical fiber for recording neu - ronal activity via eGFP expression (linked to gonadotropin major cellular organelles involved in reactive oxygen spe- cies (ROS) signaling are mitochondria and peroxisomes. releasing hormone), and (2) a newly designed animal cage whereby the floor rotates in response to head movements, Like many intracellular http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Histochemistry and Cell Biology Springer Journals

[InlineMediaObject not available: see fulltext.] In focus in HCB

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Publisher
Springer Berlin Heidelberg
Copyright
Copyright © 2017 by Springer-Verlag GmbH Germany
Subject
Biomedicine; Biomedicine, general; Cell Biology; Biochemistry, general; Developmental Biology
ISSN
0948-6143
eISSN
1432-119X
D.O.I.
10.1007/s00418-017-1598-9
Publisher site
See Article on Publisher Site

Abstract

Histochem Cell Biol (2017) 148:217–218 DOI 10.1007/s00418-017-1598-9 EDITORIAL In focus in HCB 1 2 Douglas J. Taatjes  · Jürgen Roth   Accepted: 12 July 2017 / Published online: 19 July 2017 © Springer-Verlag GmbH Germany 2017 New system for monitoring brain neuronal activity thus offers a novel means to monitor and image fluores - cently labeled neurons in deep regions of an awake and in moving rats active rat. One of the great challenges in live animal imaging is the accurate recording of brain neuronal activity in a free-mov- Rotenone effect on peroxisomal dynamics ing animal. Although multiphoton confocal microscopy has been used successfully to image more peripheral regions mediated by microtubules of the brain (Kerr et al. 2005), deeper regions remain inac- cessible. Iijima et al. (2017) have now developed a system Redox biology is an area of great interest for cell biologi- cal responses in health and disease (Little et al. 2017). Two consisting of (1) a single optical fiber for recording neu - ronal activity via eGFP expression (linked to gonadotropin major cellular organelles involved in reactive oxygen spe- cies (ROS) signaling are mitochondria and peroxisomes. releasing hormone), and (2) a newly designed animal cage whereby the floor rotates in response to head movements, Like many intracellular

Journal

Histochemistry and Cell BiologySpringer Journals

Published: Jul 19, 2017

References

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