Name: Splitting of Murine Retina for Immunofluorescence Analysis
Uploaded: 2024-01-16T11:00:00
Duration: 1 min 52 s
Description: Watch this Scientific Journal Video about Splitting of Murine Retina for Immunofluorescence Analysis at JoVE.com

splitting of murine retina for immunofluorescence analysis

マウス分裂網膜における双極性および水平神経細胞の研究

The retina is a thin neural tissue located in the posterior eye where light is intercepted and processed into an electrochemical signal that can be interpreted by the brain. At the back of the retina, rod and cone photoreceptors are stimulated by light, which reduces the tonic release rate of the neurotransmitter, glutamate1. The first neurons to experience and respond to this light-induced change in glutamate concentration are the bipolar cells (BCs) and horizontal cells (HCs), whose somas reside in the outermost region of the inner nuclear layer (INL). These second-order neurons perform the first stage of signal processing in the retina and shape critical features of vision such as light adaptation, contrast sensitivity, and spatial/color opponency2. While these functions have been ascribed to BCs and HCs, the circuitry and biochemical mechanisms underlying these processes are not fully understood3. Therefore, the advancement of tools and methods for exploring BC and HC physiology is of paramount importance.
Vertical (transverse) retina sections have long&#160;proven the most practical model for studying BCs and HCs; however, certain aspects of BC and HC physiology are inaccessible to the experimenter under this model. Direct recordings from HCs or indirect measurements of their effects on BCs do not reflect the retina&#39;s endogenous connectivity since the lateral processes of these cells are severed during slicing. Whole mount retina preparations circumvent this issue by preserving these lateral processes, but the surrounding retinal layers pose a challenge for accessing these cells4. While there are abundant examples of immunostaining5,6,7,8 and patch clamp recordings9 from INL neurons in whole mount retinas, there is an opportunity to expedite and simplify the collection of these data. The inherent limitations of transverse sections and the challenges of the whole mount model thus inspired the development of this alternative flatmount retina preparation.
The following work describes a protocol for easily removing the photoreceptor layer from live, flatmount retinas to enhance access to BCs and HCs for simplified patch clamping and faster, more efficient immunolabeling. Peeling apart two pieces of nitrocellulose membrane attached to either side of an isolated retina tears the tissue through the photoreceptor axons, leaving a split retina that retains the outer plexiform layer (OPL) and all inner retinal layers. While others have described protocols for mechanically separating layers of the retina, these methods are either poorly suited to patch clamping and microscopy applications or require tedious manipulation of the tissue. Several of these methods require frozen or lyophilized tissue for layer separation, making them incompatible with electrophysiology experiments10,11,12. Others are designed for live tissue, but necessitate 5-15 sequential peels with filter paper4,11 or treatment with trypsin13 to remove the photoreceptors. The technique described here improves upon its predecessors by simplifying the photoreceptor removal procedure and expanding the repertoire of downstream applications.

著者スポットライト:Split Retina技術を使用してアクセスを強化し、実験を加速する 

脊椎動物の網膜の内核層ニューロンを研究するための改良されたフラットマウント調製としてのスプリット網膜

Our group is interested in the neuronal circuitry and synaptic mechanisms underlying visual processing in the retina. The Morgans Lab is investigating molecular mechanisms of light adaptation in bipolar cells, and the Sivyer Lab is interested in how inner retinal neurons contribute to ganglion cell function. Accessing internuclear layer neurons in whole mount retina is a challenge for both anatomical and physiological studies.Internuclear layer neurons are accessible in vertical sections, but they're very few neurons in the field of view. Furthermore, slicing severs lateral processes and connections which can impact physiological studies. The removal of the photoreceptors in the split retina technique dramatically improves antibody diffusion into the inner retina, which makes immunolabeling of inner retinal targets over 20 times faster when compared to traditional whole mount retina.The split retina also greatly improves access to internuclear layer neurons during patch clamp electrophysiology. The split retina technique will open doors to new approaches and accelerate the pace of our experiments. For example, we plan to use this technique to study bipolar cell inputs to melanopsin ganglion cells by expressing channelrhodopsin in the bipolar cells.

Watch this Scientific Journal Video about Splitting of Murine Retina for Immunofluorescence Analysis at JoVE.com

Splitting of Murine Retina for Immunofluorescence Analysis  

免疫蛍光分析のためのマウス網膜の分割

まず、マウスの網膜が入ったペトリ皿のエイム培地を、新しいカーボゲン化エイムズと交換します。広口トランスファーピペットを使用して、解剖したマウス網膜の一部を、神経節細胞側を上にしてスライドガラスに置きます。デリケートなタスクワイプで余分な液体を取り除き、平らにします。必要に応じて、細い先端の絵筆を使用して、解剖顕微鏡の下で網膜の端をそっと引っ張ります。鉗子を使用して、乾燥したニトロセルロース膜を網膜に配置し、神経節細胞側に接着します。網膜を裏返してスライドガラスにニトロセルロースを置き、網膜の感光体側に別の乾燥膜片を置きます。次に、絵筆の先端をエイムズメディアで濡らします。上膜に穏やかな下向きの圧力をかけて、均一な接着を助けます。次に、1対の鉗子で下膜をガラスに固定します。次に、別のペアを慎重に使用して、ゆっくりと安定した動きで上膜をはがします。視細胞を含む上膜を廃棄します。最後に、内側の網膜を含む下膜を炭化エーム培地に戻します。

splitting-of-murine-retina-for-immunofluorescence-analysis

Research

JoVE Journal

Neuroscience

Splitting of Murine Retina for Immunofluorescence Analysis

Split Retina as an Improved Flatmount Preparation for Studying Inner Nuclear Layer Neurons in Vertebrate Retina

Bipolar cells and horizontal cells of the vertebrate retina are the first neurons to process visual information after photons are detected by photoreceptors. They perform fundamental operations such as light adaptation, contrast sensitivity, and spatial and color opponency. A complete understanding of the precise circuitry and biochemical mechanisms that govern their behavior will advance visual neuroscience research and ophthalmological medicine. However, current preparations for examining bipolar and horizontal cells (retinal whole mounts and vertical slices) are limited in their capacity to capture the anatomy and physiology of these cells. In this work, we present a method for removing photoreceptor cell bodies from live, flatmount mouse retinas, providing enhanced access to bipolar and horizontal cells for efficient patch clamping and rapid immunolabeling. Split retinas are prepared by sandwiching an isolated mouse retina between two pieces of nitrocellulose, then gently peeling them apart. The separation splits the retina just above the outer plexiform layer to yield two pieces of nitrocellulose, one containing the photoreceptor cell bodies and another containing the remaining inner retina. Unlike vertical retina slices, the split retina preparation does not sever the dendritic processes of inner retinal neurons, allowing for recordings from bipolar and horizontal cells that integrate the contributions of gap junction-coupled networks and wide-field amacrine cells. This work demonstrates the versatility of this preparation for the study of horizontal and bipolar cells in electrophysiology, immunohistochemistry, and in situ hybridization experiments.

This work presents an alternative flatmount retina preparation in which the removal of photoreceptor cell bodies enables faster antibody diffusion and improved patch pipette access to inner retinal neurons for immunohistochemistry, in situ hybridization, and electrophysiology experiments.