A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq

Abstract Purpose To overcome the risk of cellular damage and RNA degradation caused by high temperatures and cellular damage induced by laser capture microdissection (LCM) during plant single cell or small cell cluster isolation, we developed a rapid and simple method for single-cell separation and...

Full description

Saved in:
Bibliographic Details
Main Authors: Ruoshi Li, Mengmeng Wu, Shunlu Chen, Lan Huang, Can Wang, Zhiyin Yu, Feng Huang, Xiaofen Liu, Nianyin Zhu, Chi Song, Guihua Jiang, Xianmei Yin
Format: Article
Language:English
Published: BMC 2025-08-01
Series:Plant Methods
Subjects:
Online Access:https://doi.org/10.1186/s13007-025-01425-1
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849333553851006976
author Ruoshi Li
Mengmeng Wu
Shunlu Chen
Lan Huang
Can Wang
Zhiyin Yu
Feng Huang
Xiaofen Liu
Nianyin Zhu
Chi Song
Guihua Jiang
Xianmei Yin
author_facet Ruoshi Li
Mengmeng Wu
Shunlu Chen
Lan Huang
Can Wang
Zhiyin Yu
Feng Huang
Xiaofen Liu
Nianyin Zhu
Chi Song
Guihua Jiang
Xianmei Yin
author_sort Ruoshi Li
collection DOAJ
description Abstract Purpose To overcome the risk of cellular damage and RNA degradation caused by high temperatures and cellular damage induced by laser capture microdissection (LCM) during plant single cell or small cell cluster isolation, we developed a rapid and simple method for single-cell separation and trace RNA extraction. The extracted RNA can be used for Smart-seq analysis, enabling comprehensive studies of various cell types. Method We used the secretory cells of Ligusticum chuanxiong Hort. fibrous root. First, we performed paraffin embedding to maintain RNA stability, and then examined the optimal slice thickness to obtain intact secretory cells. We compared the RNA quality of secretory cells isolated by LCM versus manual dissection under a microscope with a scalpel. Finally, xylene was introduced into the lysis buffer, followed by rapid shaking to achieve simultaneous dewaxing and cell lysis, and the xylene layer was then removed by centrifugation. Result A slice thickness of $$20\,\mu \text {m}$$ 20 μ m best preserved the integrity of secretory cells. Compared with LCM, this method yielded higher quality RNA. The obtained transcriptomic data showed an average Q30 score exceeding 91% and a genome mapping rate surpassing 86%. Conclusion This method can yield high-quality trace RNA suitable for Smart-seq analysis. Moreover, the significant differences in the transcriptomes of various small cell clusters types demonstrate the effectiveness and specificity of our manual dissection method.
format Article
id doaj-art-3bd650c5d0c84adbaa3f3fc4b41816f0
institution Kabale University
issn 1746-4811
language English
publishDate 2025-08-01
publisher BMC
record_format Article
series Plant Methods
spelling doaj-art-3bd650c5d0c84adbaa3f3fc4b41816f02025-08-20T03:45:49ZengBMCPlant Methods1746-48112025-08-0121111210.1186/s13007-025-01425-1A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seqRuoshi Li0Mengmeng Wu1Shunlu Chen2Lan Huang3Can Wang4Zhiyin Yu5Feng Huang6Xiaofen Liu7Nianyin Zhu8Chi Song9Guihua Jiang10Xianmei Yin11State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineInstitute of Herbgenomics, Chengdu University of Traditional Chinese MedicineInstitute of Herbgenomics, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineInstitute of Herbgenomics, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineState Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese MedicineAbstract Purpose To overcome the risk of cellular damage and RNA degradation caused by high temperatures and cellular damage induced by laser capture microdissection (LCM) during plant single cell or small cell cluster isolation, we developed a rapid and simple method for single-cell separation and trace RNA extraction. The extracted RNA can be used for Smart-seq analysis, enabling comprehensive studies of various cell types. Method We used the secretory cells of Ligusticum chuanxiong Hort. fibrous root. First, we performed paraffin embedding to maintain RNA stability, and then examined the optimal slice thickness to obtain intact secretory cells. We compared the RNA quality of secretory cells isolated by LCM versus manual dissection under a microscope with a scalpel. Finally, xylene was introduced into the lysis buffer, followed by rapid shaking to achieve simultaneous dewaxing and cell lysis, and the xylene layer was then removed by centrifugation. Result A slice thickness of $$20\,\mu \text {m}$$ 20 μ m best preserved the integrity of secretory cells. Compared with LCM, this method yielded higher quality RNA. The obtained transcriptomic data showed an average Q30 score exceeding 91% and a genome mapping rate surpassing 86%. Conclusion This method can yield high-quality trace RNA suitable for Smart-seq analysis. Moreover, the significant differences in the transcriptomes of various small cell clusters types demonstrate the effectiveness and specificity of our manual dissection method.https://doi.org/10.1186/s13007-025-01425-1Laser capture microdissectionSmart-seqParaffin sectionCell IsolationLigusticum chuanxiong Hort
spellingShingle Ruoshi Li
Mengmeng Wu
Shunlu Chen
Lan Huang
Can Wang
Zhiyin Yu
Feng Huang
Xiaofen Liu
Nianyin Zhu
Chi Song
Guihua Jiang
Xianmei Yin
A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
Plant Methods
Laser capture microdissection
Smart-seq
Paraffin section
Cell Isolation
Ligusticum chuanxiong Hort
title A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
title_full A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
title_fullStr A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
title_full_unstemmed A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
title_short A cell isolation method from Ligusticum chuanxiong Hort. suitable for obtaining high-quality RNA for Smart-seq
title_sort cell isolation method from ligusticum chuanxiong hort suitable for obtaining high quality rna for smart seq
topic Laser capture microdissection
Smart-seq
Paraffin section
Cell Isolation
Ligusticum chuanxiong Hort
url https://doi.org/10.1186/s13007-025-01425-1
work_keys_str_mv AT ruoshili acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT mengmengwu acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT shunluchen acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT lanhuang acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT canwang acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT zhiyinyu acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT fenghuang acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT xiaofenliu acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT nianyinzhu acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT chisong acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT guihuajiang acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT xianmeiyin acellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT ruoshili cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT mengmengwu cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT shunluchen cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT lanhuang cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT canwang cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT zhiyinyu cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT fenghuang cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT xiaofenliu cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT nianyinzhu cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT chisong cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT guihuajiang cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq
AT xianmeiyin cellisolationmethodfromligusticumchuanxionghortsuitableforobtaininghighqualityrnaforsmartseq