The video outlines a procedure for processing DRG tissue from a mouse's spinal cord. It details steps for fixing the tissue in formaldehyde, embedding it in OCT compound, and using a cryostat to cut the tissue into 30-micrometer slices for further analysis, ensuring proper orientation and embedding techniques.

dorsal root ganglion (drg) sample preparation for cryosectioning

小鼠背根神经节冷冻切片

The dorsal root ganglion (DRG) contains the primary sensory neurons, the tissue macrophages, and the satellite cells that surround the primary sensory neurons1,2,3,4. It is a key anatomic structure in processing innocuous and noxious signals, and plays critical roles in pain, itch, and various peripheral nerve disorders5,6,7,8,9,10,11,12,13. Although several methods have been developed to dissect DRG tissue from the mouse spinal cord14,15,16, cryosectioning of the DRG tissue remains challenging as the DRG tissue is quite small, and cryostat sections of DRG samples tend to curve into rolls, making it difficult to properly transfer the cryostat sections onto glass slides. However, proper cryosectioning of the DRG tissue is crucial for immunohistochemistry studies and the structure of DRG sensory neurons17,18,19,20,21,22,23. Moreover, as single-cell RNA sequencing results have revealed the remarkable heterogeneity of DRG sensory neurons in both humans24 and mice25, proper cryosectioning of DRG tissue is critical for investigating the functional role of different DRG cells in various physiological and pathological conditions.
Although the tissue-clearing technique has been applied to investigate the 3D reconstruction of the DRG26 as an alternative technique of cryosectioning the DRG, the tissue-clearing technique is time- and labor-consuming. In comparison, cryosectioning of the DRG is quick and relatively easy to perform, and thus it remains to be a key technique for immunohistochemistry and structure studies of the DRG and other regions of the central nervous system. However, obtaining high-quality, intact, and flat cryostat sections onto glass slides remains to be a challenge in neuroscience research because of the tiny sample size of tissues, like the DRG and certain brain regions, and there is no article describing the optimal protocol at this point for cryosectioning small-sized tissue samples, such as mouse DRGs.
This protocol provides an easy, step-by-step technique for cryostat sectioning of the mouse DRG to reliably obtain as many high-quality DRG sections on the slides for subsequent DRG studies. While specifically designed for cryosectioning DRG samples, this technique can potentially be used for cryosectioning various other tissues with a small sample size.

作者聚焦：小鼠背根神经节冷冻切片程序  

小鼠背根神经节冷冻切片的程序

Watch this Scientific Journal Video about Dorsal Root Ganglion DRG Sample Preparation for Cryosectioning at JoVE.com

Dorsal Root Ganglion (DRG) Sample Preparation for Cryosectioning  

用于冷冻切片的背根神经节 （DRG） 样品制备

首先在室温下将麻醉小鼠脊髓中解剖的DRG组织在4%甲醛中固定3小时。然后，将组织在 30% 蔗糖的 PBS 中，在 4 摄氏度下孵育过夜。接下来，通过添加 OCT 化合物并覆盖铝块的顶面来准备基础 OCT。将覆盖的铝块在零下 20 摄氏度下冷冻 5 到 10 分钟。使用低温恒温器切掉 30 微米厚的 OCT 顶部，直到其表面与底座 OCT 一样平坦。 在将铝块从低温恒温器上取下之前，在 6：00 位置标记底座 OCT 的底部。要进行DRG的OCT包埋，请将DRG组织放在干燥的培养皿上，然后用干燥的镊子将其从一个位置移动到另一个位置两到三次，从而干燥DRG组织。然后，使用干镊子将干燥的 DRG 放在 12：00 位置的 OCT 底座上。确保 DRG 的上边缘和基础 OCT 的上边缘之间至少保持 5 毫米的距离，背部在 12：00 位置，腹侧在 6：00 位置。接下来，将 OCT 添加为圆形或椭圆形，以嵌入整个 DRG 组织，并将 DRG 置于中心。将覆盖的OCT和DRG样品在零下20摄氏度下冷冻5分钟。完成后，切掉 30 微米厚的盖子 OCT 顶部，直到 DRG 可见。

dorsal-root-ganglion-drg-sample-preparation-for-cryosectioning

Research

JoVE Journal

Neuroscience

Dorsal Root Ganglion (DRG) Sample Preparation for Cryosectioning

689 次观看. 首先在室温下将麻醉小鼠脊髓中解剖的DRG组织在4%甲醛中固定3小时。然后，将组织在 30% 蔗糖的 PBS 中，在 4 摄氏度下孵育过夜。接下来，通过添加 OCT 化合物并覆盖铝块的顶面来准备基础 OCT。将覆盖的铝块在零下 20 摄氏度下冷冻 5 到 10 分钟。使用低温恒温器切掉 30 微米厚的 OCT 顶部，直到其表面与底座 OCT 一样平坦。 在将铝块从低温恒温器上取下之前，在 6：00 位置?...

视频: Dorsal Root Ganglion (DRG) Sample Preparation for Cryosectioning  

A Procedure for Mouse Dorsal Root Ganglion Cryosectioning

High-quality mouse dorsal root ganglion (DRG) cryostat sections are crucial for proper immunochemistry staining and RNAscope studies in the research of inflammatory and neuropathic pain, itch, as well as other peripheral neurological conditions. However, it remains a challenge to consistently obtain high-quality, intact, and flat cryostat sections onto glass slides because of the tiny sample size of the DRG tissue. So far, there is no article describing an optimal protocol for DRG cryosectioning. This protocol presents a step-by-step method to resolve the frequently encountered difficulties associated with DRG cryosectioning. The presented article explains how to remove the surrounding liquid from the DRG tissue samples, place the DRG sections on the slide facing the same orientation, and flatten the sections on the glass slide without curving up. Although this protocol has been developed for cryosectioning the DRG samples, it can be applied for the cryosectioning of many other tissues with a small sample size.

Presented here is the development for consistently acquiring high-quality dorsal root ganglion cryostat sections.

High-quality mouse dorsal root ganglion (DRG) cryostat sections are crucial for proper immunochemistry staining and RNAscope studies in the research of ...