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RevGel-seq:使用可逆水凝胶进行细胞特异性标记的无仪器单细胞 RNA 测序。

RevGel-seq: instrument-free single-cell RNA sequencing using a reversible hydrogel for cell-specific barcoding.

机构信息

Scipio Bioscience, Paris, France.

Skyhawk Therapeutics, Basel, Switzerland.

出版信息

Sci Rep. 2023 Mar 24;13(1):4866. doi: 10.1038/s41598-023-31915-y.

DOI:10.1038/s41598-023-31915-y
PMID:36964177
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10039079/
Abstract

Progress in sample preparation for scRNA-seq is reported based on RevGel-seq, a reversible-hydrogel technology optimized for samples of fresh cells. Complexes of one cell paired with one barcoded bead are stabilized by a chemical linker and dispersed in a hydrogel in the liquid state. Upon gelation on ice the complexes are immobilized and physically separated without requiring nanowells or droplets. Cell lysis is triggered by detergent diffusion, and RNA molecules are captured on the adjacent barcoded beads for further processing with reverse transcription and preparation for cDNA sequencing. As a proof of concept, analysis of PBMC using RevGel-seq achieves results similar to microfluidic-based technologies when using the same original sample and the same data analysis software. In addition, a clinically relevant application of RevGel-seq is presented for pancreatic islet cells. Furthermore, characterizations carried out on cardiomyocytes demonstrate that the hydrogel technology readily accommodates very large cells. Standard analyses are in the 10,000-input cell range with the current gelation device, in order to satisfy common requirements for single-cell research. A convenient stopping point after two hours has been established by freezing at the cell lysis step, with full preservation of gene expression profiles. Overall, our results show that RevGel-seq represents an accessible and efficient instrument-free alternative, enabling flexibility in terms of experimental design and timing of sample processing, while providing broad coverage of cell types.

摘要

报道了基于 RevGel-seq 的 scRNA-seq 样本制备进展,这是一种针对新鲜细胞样本优化的可逆水凝胶技术。一个细胞与一个带有条形码的珠子的复合物通过化学连接剂稳定,并在液态下分散在水凝胶中。在冰上凝胶化时,复合物被固定并物理分离,而无需纳米孔或液滴。通过去污剂扩散触发细胞裂解,RNA 分子被捕获在相邻的带有条形码的珠子上,用于进一步进行逆转录和 cDNA 测序准备。作为概念验证,使用 RevGel-seq 对 PBMC 的分析在使用相同原始样本和相同数据分析软件时,可获得与微流控技术相似的结果。此外,还提出了 RevGel-seq 在胰岛细胞方面的临床相关应用。此外,对心肌细胞进行的表征表明,水凝胶技术可以轻松容纳非常大的细胞。在当前的凝胶化设备中,标准分析可达到 10,000 个输入细胞的范围,以满足单细胞研究的常见要求。通过在细胞裂解步骤中冷冻建立了一个方便的两小时停止点,同时充分保留基因表达谱。总体而言,我们的结果表明 RevGel-seq 代表了一种易于获得且高效的无仪器替代方案,在实验设计和样本处理时间方面具有灵活性,同时提供了广泛的细胞类型覆盖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/af4533ed0cfb/41598_2023_31915_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/283331cb1f01/41598_2023_31915_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/1ac6c907a7e1/41598_2023_31915_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/fa618b066251/41598_2023_31915_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/bde769f986b2/41598_2023_31915_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/af4533ed0cfb/41598_2023_31915_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/283331cb1f01/41598_2023_31915_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/1ac6c907a7e1/41598_2023_31915_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/fa618b066251/41598_2023_31915_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/bde769f986b2/41598_2023_31915_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ed/10039079/af4533ed0cfb/41598_2023_31915_Fig5_HTML.jpg

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