Name: Wide-Field Calcium Imaging of Mouse Superior Colliculus Neurons
Uploaded: 2023-04-21T15:00:00
Description: Watch this Scientific Journal Video about Wide-Field Calcium Imaging of Mouse Superior Colliculus Neurons at JoVE.com

wide-field calcium imaging of mouse superior colliculus neurons

सुपीरियर कोलिकुलस में दो-फोटॉन और वाइड-फील्ड कैल्शियम इमेजिंग

The superior colliculus (SC) is an important visual center in all vertebrates. In mammals, it receives direct inputs from the retina and the visual cortex1. While optical recording has been widely applied to the cortex2,3,4,5, its application in the SC is hindered by poor optical accesss6,7,8,9,10,11,12,13,14,15,16,17,18,19. The goal of this protocol is to provide details about two complementary methods for optical recording of the neural activity in the SC.
The SC is located beneath the cortex and transverse sinus, which limits optical access to the collicular neurons. One approach to overcome this limitation is to aspirate the overlaying cortex and expose the anterior-lateral SC7,9,10,13,14,19. However, because the SC receives cortical inputs, such an operation might affect how the SC neurons respond to visual stimuli. To overcome this limitation, we detail here an alternative protocol to image the superficial layer of the posterior-medial SC with a silicon plug, while leaving the cortex intact8,11. Specifically, to achieve single-cell resolution, we applied two-photon microscopy to image calcium responses in the posterior-medial SC of wild-type mice. In addition, to achieve broad coverage, we applied wide-field microscopy to image the entire SC of a mutant mouse whose posterior cortex has not developed20.
The two methods described in this protocol are complementary to each other. The two-photon calcium imaging without ablating the cortex is appropriate for recording neural activity at&#160;single-cell resolution with intact cortical inputs. The wide-field calcium imaging is appropriate for recording neural activity in the entire SC while sacrificing spatial resolution.

लेखक स्पॉटलाइट: सुपीरियर कोलिकुलस में तंत्रिका कोडिंग और दृश्य प्रसंस्करण के तंत्र का अनावरण 

माउस सुपीरियर कोलिकुलस में कैल्शियम इमेजिंग

My research focuses on neural coding and mechanisms for visual processing. We are trying to answer how various information is encoded in the brain, especially in the superior colliculus under the underlying neuro-mechanisms. To understand visual processing, scientists combine various approaches, including neuronal morphology, antegrade and retrograde tracing, IL sequencing, neuro modeling, machine learning, is understood well.The challenge is to remove the skull over the SSA, cutting and left in the bone in one larger piece, is likely to fail because the bone is attached to the dura. By combining two photo on a wide field calcium image, our recent work revealed the function architecture of motion direction in the mouse SC at both single cell resolution and a global scale. We found that neurons with similar preference form patches up to 500 micrometer under global to the upward on the nasal motion.With our protocol, we are addressing two research gaps. First, researchers can perform long-term cast imaging in mouse SC at a single cell resolution without breaking the cortex. Secondly, researchers can record the neuroactivity across the entire SC using widefield microscoping.Our protocol provides a measure to image the posterior medial SC at single cell resolution with a intact cortex in mice. Also, we use a biocompatible plug to expose the SC, which reduces infection for chronic imaging. Our results provide a way to study the neural coding of visual information across a large visual field.Combined with optogenetics, one can study half inputs from different brain regions modulating the neuroactivity in SC.

Watch this Scientific Journal Video about Wide-Field Calcium Imaging of Mouse Superior Colliculus Neurons at JoVE.com

Wide-Field Calcium Imaging of Mouse Superior Colliculus Neurons  

माउस सुपीरियर कोलिकुलस न्यूरॉन्स की वाइड-फील्ड कैल्शियम इमेजिंग

शुरू करने के लिए, एससी के प्रत्येक तरफ के केंद्र में 200 माइक्रोमीटर की गहराई पर जीसीएएमपी 6 एम को व्यक्त करने वाले एएवी के 100 नैनोलीटर को उत्परिवर्ती माउस में इंजेक्ट करें, जिसका पिछला कॉर्टेक्स विकसित करने में विफल रहा है। लगभग तीन सप्ताह के बाद, एससी के ऊपर पांच मिलीमीटर व्यास की कवर स्लिप प्रत्यारोपित करें। कवर स्लिप को ठीक करने के बाद, 10 हर्ट्ज पर उत्सर्जन फिल्टर पास करने के बाद सीएमओए कैमरे का उपयोग करके चित्र प्राप्त करें। आंशिक कॉर्टेक्स उत्परिवर्ती माउस से एससी न्यूरॉन्स की कैल्शियम प्रतिक्रियाओं को वाइड-फील्ड माइक्रोस्कोपी का उपयोग करके चित्रित किया गया था।अधिग्रहित छवि को मूल आकार के एक चौथाई तक नमूना दिया गया था, और नेत्रहीन कैल्शियम प्रतिक्रियाएं दिखाई गई हैं।

Research

JoVE Journal

Neuroscience

Wide-Field Calcium Imaging of Mouse Superior Colliculus Neurons

Calcium Imaging in Mouse Superior Colliculus

The superior colliculus (SC), an evolutionarily conserved midbrain structure in all vertebrates, is the most sophisticated visual center before the ...

Preparation of a Suction Cup and Plugs for Calcium Imaging in Mouse

माउस में कैल्शियम इमेजिंग के लिए एक सक्शन कप और प्लग की तैयारी

Viral Construct (AAV) Injection in Mouse Superior Colliculus for Calcium Imaging

कैल्शियम इमेजिंग के लिए माउस सुपीरियर कोलिकुलस में वायरल कंस्ट्रक्ट (एएवी) इंजेक्शन

Implantation of the Headplate in Mouse for Calcium Imaging 

कैल्शियम इमेजिंग के लिए माउस में हेडप्लेट का प्रत्यारोपण 

Implanting the Plug in the Mouse for Calcium Imaging

कैल्शियम इमेजिंग के लिए माउस में प्लग प्रत्यारोपित करना

Two-Photon Calcium Imaging of Mouse Superior Colliculus Neurons

माउस सुपीरियर कोलिकुलस न्यूरॉन्स के दो-फोटॉन कैल्शियम इमेजिंग