Evidence map›Paper›PMID 34717753›Full record

ArticleStem cell research & therapy2021

Single cell Raman spectroscopy to identify different stages of proliferating human hepatocytes for cell therapy.

Chen Ma, Ludi Zhang, Ting He, Huiying Cao, Xiongzhao Ren, Chenhui Ma, Jiale Yang, Ruimin Huang, Guoyu Pan

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chen MaShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ludi ZhangState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China.
Ting HeSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, China.
Huiying CaoShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Xiongzhao RenState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Institute of Biochemistry and Cell Biology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, 200031, China.
Chenhui MaShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Jiale YangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ruimin HuangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. rmhuang@simm.ac.cn.ORCID 0000-0001-9369-0263
Guoyu PanShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. gypan@simm.ac.cn.ORCID 0000-0002-6731-5803

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell therapy provides hope for treatment of advanced liver failure. Proliferating human hepatocytes (ProliHHs) were derived from primary human hepatocytes (PHH) and as potential alternative for cell therapy in liver diseases. Due to the continuous decline of mature hepatic genes and increase of progenitor like genes during ProliHHs expanding, it is challenge to monitor the critical changes of the whole process. Raman microspectroscopy is a noninvasive, label free analytical technique with high sensitivity capacity. In this study, we evaluated the potential and feasibility to identify ProliHHs from PHH with Raman spectroscopy.

methodsRaman spectra were collected at least 600 single spectrum for PHH and ProliHHs at different stages (Passage 1 to Passage 4). Linear discriminant analysis and a two-layer machine learning model were used to analyze the Raman spectroscopy data. Significant differences in Raman bands were validated by the associated conventional kits.

resultsLinear discriminant analysis successfully classified ProliHHs at different stages and PHH. A two-layer machine learning model was established and the overall accuracy was at 84.6%. Significant differences in Raman bands have been found within different ProliHHs cell groups, especially changes at 1003 cm

conclusionsIn brief, Raman spectroscopy was successfully employed to identify different stages of ProliHHs during dedifferentiation process. The approach can simultaneously trace multiple changes of cellular components from somatic cells to progenitor cells.

Indexed as

HepatocytesSpectrum Analysis, RamanCell- and Tissue-Based TherapyDiscriminant AnalysisHumansLiverCell therapyDedifferentiationIdentificationProliferating human hepatocytesRaman spectroscopy

Identifiers

PMID34717753
PMCPMC8556950

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