TY - JOUR
T1 - Circuit mechanisms of neurodegenerative diseases
T2 - A new frontier with miniature fluorescence microscopy
AU - Werner, Craig T.
AU - Williams, Christopher J.
AU - Fermelia, Mercedes R.
AU - Lin, Da Ting
AU - Li, Yun
N1 - Funding Information:
This research was supported by grants from NIH NIDA IRP, COBRE NIGMS (grant no. 5P20GM121310-03), and NINDS (grant nos. 1R61NS115161-01 and 1UG3NS115608-01).
Publisher Copyright:
© 2019 Werner, Williams, Fermelia, Lin and Li.
PY - 2019
Y1 - 2019
N2 - Neurodegenerative diseases (NDDs), such as Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD), are devastating age-associated brain disorders. Significant efforts have been made to uncover the molecular and cellular pathogenic mechanisms that underlie NDDs. However, our understanding of the neural circuit mechanisms that mediate NDDs and associated symptomatic features have been hindered by technological limitations. Our inability to identify and track individual neurons longitudinally in subcortical brain regions that are preferentially targeted in NDDs has left gaping holes in our knowledge of NDDs. Recent development and advancement of the miniature fluorescence microscope (miniscope) has opened up new avenues for examining spatially and temporally coordinated activity from hundreds of cells in deep brain structures in freely moving rodents. In the present mini-review, we examine the capabilities of current and future miniscope tools and discuss the innovative applications of miniscope imaging techniques that can push the boundaries of our understanding of neural circuit mechanisms of NDDs into new territories.
AB - Neurodegenerative diseases (NDDs), such as Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD), are devastating age-associated brain disorders. Significant efforts have been made to uncover the molecular and cellular pathogenic mechanisms that underlie NDDs. However, our understanding of the neural circuit mechanisms that mediate NDDs and associated symptomatic features have been hindered by technological limitations. Our inability to identify and track individual neurons longitudinally in subcortical brain regions that are preferentially targeted in NDDs has left gaping holes in our knowledge of NDDs. Recent development and advancement of the miniature fluorescence microscope (miniscope) has opened up new avenues for examining spatially and temporally coordinated activity from hundreds of cells in deep brain structures in freely moving rodents. In the present mini-review, we examine the capabilities of current and future miniscope tools and discuss the innovative applications of miniscope imaging techniques that can push the boundaries of our understanding of neural circuit mechanisms of NDDs into new territories.
KW - Deep brain imaging
KW - In vivo calcium imaging
KW - Longitudinal recording
KW - Miniature fluorescence microscopy
KW - Miniscope
KW - Neurodegenerative disorders
UR - http://www.scopus.com/inward/record.url?scp=85075024561&partnerID=8YFLogxK
U2 - 10.3389/fnins.2019.01174
DO - 10.3389/fnins.2019.01174
M3 - Article
AN - SCOPUS:85075024561
SN - 1662-4548
VL - 13
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
IS - OCT
M1 - 1174
ER -