This is most recent lab
work, activated microglia surrounding amyloid plaques and dense core
stained by Thio-S
Coded murine behavior analysis, Ethovision raw data with MATLAB ploting
Illustration of various behavior modality analysis
Cre-dependent AAV-ChETA was injected in the PFC, followed by TAM
injection to induce activity-dependent cre (TRAP2 mice line). In BLA,
PFC terminals were stimulated with
blue light, which cleads
to time locked action potentials. In addition, similar approaches were
used for inhibitory opsins, where yellow light leads to
silencing of activity or hyperpolarization.
Juvenile social isolation induced labeling of activated neurons
throughout the brain.
USV is a measure of
communications, used in autism mouse models, we used machine learning to
categorize the call types and automatic analysis/plotting
One pending ABRC grant application work
graphic abstract of Aim 2 - synaptic physiology and LSPS circuit mapping
graphic abstract of Aim 3 - optogenetics and cocaine self administration
Measuring neuronal activity using GCaMP6 and fiber photometry
Multichannel in vivo recording, spikes, LFPs, phase locking
MATLAB coded analysis for sorted spikes
Fast
scanning cyclic voltametry
FSCV(https://en.wikipedia.org/wiki/Fast-scan_cyclic_voltammetry)
was used to measure fast dopamine dynamics in brain slices. This can be
useful to measure the evoked dopamine release in grafted DA neurons
following gene therapy. Carbon fiber electrode was placed in dorsal
striatum, with stimulating electrode close by. stimulation leads to DA
relase. Typical redox potential of DA is shown below.
Measure dopamine levels in brain slices using dLight DA sensor
AAV-dLight (https://pubmed.ncbi.nlm.nih.gov/33087905/) was injected into nucleus accumbens, acute slices were made, electrode stimulation leads to dynamic changes of dopamine signals. Captured at 20fps.
Using an Intan board, we recorded mouse EEG and EMG, establishing a
proof of principle for the sleep related studies. MATLAB FMAtools
toolbox is used to characterize sleep state (wakeful, quite, REM,
Non-REM, etc).
For a video, see (https://www.youtube.com/watch?v=GMrS99ddK4A). Gorgenous
‘twinkle’ of dendritics spines represent calcium changes (miniature
events) at spines.
Recent single cell RNAseq work - illustration of workflow of the 10X Genomics pipeline
A and B. Illustration of
LSPS mapping technique; C. LSPS applied to map local excitatory inputs
onto L5 projection neurons. D. Sample responses of soma,
synaptic/excitatory, and inhibitory responses. G, H. LSPS applied to map
hippocampus circuits.
Neuronal morphology analysis, spines, dendrite, IHC staining
This is a published NCBI
dataset, mild traumatic brain injury.
Our group published the first paper (https://pubmed.ncbi.nlm.nih.gov/22934102/) on single
neuron RNAseq in brain slices using patch seq in 2012. This has been
used in a few large dataset where neuronal morphology and ephys property
are explored jointly.