Mental disease, including schizophrenia, depression and autism spectrum disorders, are still poorly understood, although it is clear that they mostly represent cortical disorders. The cortex is the primary site of higher mental functions, and despite extensive research, there is still no unified theory of how the cortex works. This is partly due to the fact that neuroscientists have traditionally relied on microelectrodes to record the activity of individual cells. However, cortical circuits are composed of millions of neurons and it is conceivable that single cell measurements alone will not be sufficient to unravel function of the brain. Optical imaging techniques tackle this emergent level of neuronal circuit activity and enable to image the activity of neuronal ensembles, in vitro and in vivo, while preserving single cell resolution, something that brain imaging techniques such as MRI or PET, cannot do. Moreover, the development of genetically encoded photosensitive proteins (optogenetics) and optochemical (caged) compounds offers the opportunity to not only image the activity of many neurons but also to optically control them. Advances in optogenetics has led to the development of two-photon microscopes combined with spatial light modulators (SLM), that allow the customer to split the laser beam into a holographic pattern that can be used to image activity or photoactivate neurons simultaneously in 3D. Multiple commercially available microscopes are now offered. Additionally researchers are customizing their own microscopes as a low cost alternative to purchasing new commercially available microscopes. The Meadowlark Optics (MLO) SLM is preferentially utilized due to the unprecedented response time a factor of 8 faster than competing SLMs, enabling more complex studies of brain function. However, the limited resolution of the SLM leads to studies over a smaller volume, and low fill factor leads to optical losses. To address these concerns MLO is proposing the development of a high speed (142 Hz to 500 Hz), high fill factor (95%), high resolution SLM. To reduce cost, and time to market MLO proposes to utilize an existing backplane, representing a total savings of $1M, and 1 year of development. Meadowlark will realize a prototype system within the Phase I, and will utilize internal funds to complete the product.
Public Health Relevance Statement: Project Narrative Microscopy with spatial light modulators (SLMs) enables use of optical techniques to study neuronal circuit activity, to both monitor and manipulate the activity of neuronal ensembles, in vitro and in vivo. As a result of successful worldwide research in this field, suppliers of commercial two photon microscopes feel there is extensive product potential. As such, six major microscope suppliers have either licensed or are negotiating the patents to existing IP filed by Columbia University regarding use of photostimulation and adaptive optics in microscopy. The Meadowlark Optics SLM as a key component in these commercial microscopes used to create the volume of foci for 3D, scan-less, multi-site, programmable excitation. Development of a high resolution, high speed (142 Hz to 500 Hz) SLM will provide commercial suppliers with a second generation microscope that matches the field of view that the SLM can excite to the field of view and resolution of commercial microscopes. Additionally the SLM can be sold as a stand-alone product addressing a wide range of markets.
Project Terms: abstracting; adaptive optics; Address; Affect; autism spectrum disorder; Biological Assay; Brain; Brain imaging; Bypass; Calcium; Cells; Communication; Complex; Computer software; cost; Dendrites; design; Development; Devices; Disease; disparity reduction; Etiology; feeding; Functional disorder; Functional Magnetic Resonance Imaging; Funding; Generations; Image; Imaging Techniques; In Vitro; in vivo; Individual; Joints; Lasers; Lateral; Legal patent; Letters; Licensing; Light; liquid crystal; Location; Long-Term Effects; Magnetic Resonance Imaging; Marketing; Measurement; Mediation; meetings; Mental Depression; mental function; Microelectrodes; Microscope; Microscopy; Molecular; Monitor; neuronal circuitry; Neurons; Neurosciences; optic imaging; Optics; optogenetics; Outcome; palliative; patch clamp; Pattern; Phase; Physiologic pulse; Population; Positron-Emission Tomography; programs; Proteins; prototype; Psyche structure; Reaction Time; Research; Research Personnel; research study; Resolution; response; Rights; Savings; Scanning; Scheme; Schizophrenia; Shapes; Site; Source; Speed; stem; Structure; Synapses; System; Techniques; Technology; Testing; theories; Therapeutic; Thick; Time; tool; two-photon; Universities; Update; Work
