Lo Shun Qiang

No Thumbnail Available
Last Name
Lo
First Name
Shun Qiang
ORCID

Filters

2013 - 2017 3
3
3
Reset filters

Settings

Search Results

Now showing 1 - 3 of 3
Thumbnail Image
Article

Defining a critical period for inhibitory circuits within the somatosensory cortex

2017-08-04 , Lo, Shun Qiang , Sng, Judy C. G. , Augustine, George J.

Although experience-dependent changes in brain inhibitory circuits are thought to play a key role during the “critical period” of brain development, the nature and timing of these changes are poorly understood. We examined the role of sensory experience in sculpting an inhibitory circuit in the primary somatosensory cortex (S1) of mice by using optogenetics to map the connections between parvalbumin (PV) expressing interneurons and layer 2/3 pyramidal cells. Unilateral whisker deprivation decreased the strength and spatial range of inhibitory input provided to pyramidal neurons by PV interneurons in layers 2/3, 4 and 5. By varying the time when sensory input was removed, we determined that the critical period closes around postnatal day 14. This yields the first precise time course of critical period plasticity for an inhibitory circuit.

View
Thumbnail Image
Article

All-optical mapping of barrel cortex circuits based on simultaneous voltage-sensitive dye imaging and channelrhodopsin-mediated photostimulation

2015-03-31 , Lo, Shun Qiang , Koh, Dawn X. P. , Sng, Judy C. G. , Augustine, George J.

We describe an experimental approach that uses light to both control and detect neuronal activity in mouse barrel cortex slices: blue light patterned by a digital micromirror array system allowed us to photostimulate specific layers and columns, while a red-shifted voltage-sensitive dye was used to map out large-scale circuit activity. We demonstrate that such all-optical mapping can interrogate various circuits in somatosensory cortex by sequentially activating different layers and columns. Further, mapping in slices from whisker-deprived mice demonstrated that chronic sensory deprivation did not significantly alter feedforward inhibition driven by layer 5 pyramidal neurons. Further development of voltage-sensitive optical probes should allow this all-optical mapping approach to become an important and high-throughput tool for mapping circuit interactions in the brain.

View
Thumbnail Image
Article

Next-generation transgenic mice for optogenetic analysis of neural circuits

2013-11-26 , Asrican, Brent , Augustine, George J. , Berglund, Ken , Chen, Susu , Chow, Nick , Deisseroth, Karl , Feng, Guoping , Gloss, Bernd , Hira, Riichiro , Hoffmann, Carolin , Kasai, Haruo , Katarya, Malvika , Kim, Jinsook , Kudolo, John , Lee, Li Ming , Lo, Shun Qiang , Mancuso, James , Matsuzaki, Masanori , Nakajima, Ryuichi , Qiu, Li , Tan, Gregory , Tang, Yanxia , Ting, Jonathan T. , Tsuda, Sachiko , Wen, Lei , Zhang, Xuying , Zhao, Shengli

Here we characterize several new lines of transgenic mice useful for optogenetic analysis of brain circuit function. These mice express optogenetic probes, such as enhanced halorhodopsin or several different versions of channelrhodopsins, behind various neuron-specific promoters. These mice permit photoinhibition or photostimulation both in vitro and in vivo. Our results also reveal the important influence of fluorescent tags on optogenetic probe expression and function in transgenic mice.

View