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RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models
ETHNOPHARMACOLOGICAL RELEVANCE: Jian-yan-ling (JYL) is a drug used in traditional Chinese medicine (TCM) prescriptions for the treatment of tumors after radiotherapy and chemotherapy, to effectively alleviate leukocytopenia. However, the genetic mechanisms underlying the function of JYL remain uncle...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213199/ https://www.ncbi.nlm.nih.gov/pubmed/37251843 http://dx.doi.org/10.1016/j.heliyon.2023.e16143 |
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author | Zhang, Xiaobo Zhai, Yunliang Zhang, Dandan Che, Chang Zhang, Yayun Li, Quan Zhang, Xue Zhao, Lingrui |
author_facet | Zhang, Xiaobo Zhai, Yunliang Zhang, Dandan Che, Chang Zhang, Yayun Li, Quan Zhang, Xue Zhao, Lingrui |
author_sort | Zhang, Xiaobo |
collection | PubMed |
description | ETHNOPHARMACOLOGICAL RELEVANCE: Jian-yan-ling (JYL) is a drug used in traditional Chinese medicine (TCM) prescriptions for the treatment of tumors after radiotherapy and chemotherapy, to effectively alleviate leukocytopenia. However, the genetic mechanisms underlying the function of JYL remain unclear. AIM OF THE STUDY: This study aimed to explore the RNA changes and potential biological processes related to the anti-aging or life-extending effects of JYL treatments. MATERIALS AND METHODS: In vivo treatments were performed using Canton-S Drosophila corresponding to three groups: control, low-concentration (low-conc.), and high-concentration (high-conc.) groups. The low-conc. And the high-conc. Groups were treated with 4 mg/mL JYL and 8 mg/mL JYL, respectively. Thirty Drosophila eggs were placed in each vial, and the third instar larvae and adults 7 and 21 days post-eclosion were collected for RNA sequencing, irrespective of the gender. In vitro treatments were conducted using humanized immune cell lines HL60 and Jurkat, which were divided into 3 groups: control (0 μg/mL JYL), low-concentration (40 μg/mL JYL), and high-concentration (80 μg/mL JYL). The cells were collected after 48 h of each JYL drug treatment. Both the Drosophila and cell samples were analyzed using RNA sequencing. RESULTS: The in vivo experiments revealed 74 upregulated genes in the low-concentration group, and CG13078 was a commonly downregulated differential gene, which is involved in ascorbate iron reductase activity. Further analysis of the co-expression map identified the key genes: regulatory particle non-ATPase (RPN), regulatory particle triple-A ATPase (RPT), and tripeptidyl-peptidase II (TPP II). For the in vitro experiments, 19 co-differential genes were compared between different concentrations of the HL 60 cell line, of which three genes were upregulated: LOC107987457 (phostensin-like gene), HSPA1A (heat shock protein family A member 1 A), and H2AC19 (H2A clustered histone 19). In the HL 60 cell line, JYL activated proteasome-related functions. In the Jurkat cell line, there were no common differential genes despite the presence of a dosage-dependent trend. CONCLUSIONS: The RNA-seq results showed that the traditional Chinese medicine JYL has longevity and anti-aging effects, indicating that further investigation is required. |
format | Online Article Text |
id | pubmed-10213199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102131992023-05-27 RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models Zhang, Xiaobo Zhai, Yunliang Zhang, Dandan Che, Chang Zhang, Yayun Li, Quan Zhang, Xue Zhao, Lingrui Heliyon Research Article ETHNOPHARMACOLOGICAL RELEVANCE: Jian-yan-ling (JYL) is a drug used in traditional Chinese medicine (TCM) prescriptions for the treatment of tumors after radiotherapy and chemotherapy, to effectively alleviate leukocytopenia. However, the genetic mechanisms underlying the function of JYL remain unclear. AIM OF THE STUDY: This study aimed to explore the RNA changes and potential biological processes related to the anti-aging or life-extending effects of JYL treatments. MATERIALS AND METHODS: In vivo treatments were performed using Canton-S Drosophila corresponding to three groups: control, low-concentration (low-conc.), and high-concentration (high-conc.) groups. The low-conc. And the high-conc. Groups were treated with 4 mg/mL JYL and 8 mg/mL JYL, respectively. Thirty Drosophila eggs were placed in each vial, and the third instar larvae and adults 7 and 21 days post-eclosion were collected for RNA sequencing, irrespective of the gender. In vitro treatments were conducted using humanized immune cell lines HL60 and Jurkat, which were divided into 3 groups: control (0 μg/mL JYL), low-concentration (40 μg/mL JYL), and high-concentration (80 μg/mL JYL). The cells were collected after 48 h of each JYL drug treatment. Both the Drosophila and cell samples were analyzed using RNA sequencing. RESULTS: The in vivo experiments revealed 74 upregulated genes in the low-concentration group, and CG13078 was a commonly downregulated differential gene, which is involved in ascorbate iron reductase activity. Further analysis of the co-expression map identified the key genes: regulatory particle non-ATPase (RPN), regulatory particle triple-A ATPase (RPT), and tripeptidyl-peptidase II (TPP II). For the in vitro experiments, 19 co-differential genes were compared between different concentrations of the HL 60 cell line, of which three genes were upregulated: LOC107987457 (phostensin-like gene), HSPA1A (heat shock protein family A member 1 A), and H2AC19 (H2A clustered histone 19). In the HL 60 cell line, JYL activated proteasome-related functions. In the Jurkat cell line, there were no common differential genes despite the presence of a dosage-dependent trend. CONCLUSIONS: The RNA-seq results showed that the traditional Chinese medicine JYL has longevity and anti-aging effects, indicating that further investigation is required. Elsevier 2023-05-19 /pmc/articles/PMC10213199/ /pubmed/37251843 http://dx.doi.org/10.1016/j.heliyon.2023.e16143 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Zhang, Xiaobo Zhai, Yunliang Zhang, Dandan Che, Chang Zhang, Yayun Li, Quan Zhang, Xue Zhao, Lingrui RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title | RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title_full | RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title_fullStr | RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title_full_unstemmed | RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title_short | RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models |
title_sort | rnaseq analysis of the drug jian-yan-ling (jyl) using both in vivo and in vitro models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213199/ https://www.ncbi.nlm.nih.gov/pubmed/37251843 http://dx.doi.org/10.1016/j.heliyon.2023.e16143 |
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