Effects of Panaxadiol Saponins Component as A New Chinese Patent Medicine on Proliferation, Differentiation and Corresponding Gene Expression Profile of Megakaryocytes
Objective: To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gone expression profile of megakaryocytes. Methods: Bone marrow culture of colony forming assay of megakaryocytic progenito...
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| Published in | Chinese journal of integrative medicine Vol. 22; no. 1; pp. 28 - 35 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
Beijing
Chinese Association of Traditional and Western Medicine
01.01.2016
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1672-0415 1993-0402 |
| DOI | 10.1007/s11655-015-1970-3 |
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| Abstract | Objective: To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gone expression profile of megakaryocytes. Methods: Bone marrow culture of colony forming assay of megakaryocytic progenitor cells (CFU-MK) was observed for the promoting proliferation mediated by PDS-C, and differentiation of megakaryocytic blasts caused by PDS-C was analyzed with flow cytometry in CHRF-288 and Meg-01 cells, as well as proliferation, differentiation-related genes expression profile and protein expression levels were detected by human gone expression microarray and western blot. Results: In response to PDS-C 10, 20 and 50 mg/L, CFU-MK from 10 human bone marrow samples was increased by 28.9± 2.7%, 41.0% ± 3.2% and 40.5% ± 2.6% over untreated control, respectively (P〈0.01, each). Flow cytometry analysis showed that PDS-C treated CHRF-288 cells and Meg-01 cells significantly increased in CD42b, CD41, TSP and CD36 positive ratio, respectively. PDS-C induced 29 genes up-regulated more than two-fold commonly in both cells detected by human expression microarray representing 4000 known genes. The protein expression levels of ZNF91, c-Fos, BTF3a, GATA-1, RGS2, NDRG2 and RUNX1 were increased with western blot in correspond to microarray results. Conclusion: PDS-C as an effective component for hematopoiesis, play the role to enhance proliferation and differentiation of megakaryocytes, also up-regulated expression of proliferation, differentiation-related genes and proteins in vitro. KEYWORDS panaxadiol saponins, megakaryocyte, gone expression profile, proliferation, differentiation |
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| AbstractList | To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gene expression profile of megakaryocytes.
Bone marrow culture of colony forming assay of megakaryocytic progenitor cells (CFU-MK) was observed for the promoting proliferation mediated by PDS-C, and differentiation of megakaryocytic blasts caused by PDS-C was analyzed with flow cytometry in CHRF-288 and Meg-01 cells, as well as proliferation, differentiation-related genes expression profile and protein expression levels were detected by human gene expression microarray and western blot.
In response to PDS-C 10, 20 and 50 mg/L, CFU-MK from 10 human bone marrow samples was increased by 28.9%±2.7%, 41.0%±3.2% and 40.5%±2.6% over untreated control, respectively (P <0.01, each). Flow cytometry analysis showed that PDS-C treated CHRF-288 cells and Meg-01 cells significantly increased in CD42b, CD41, TSP and CD36 positive ratio, respectively. PDS-C induced 29 genes up-regulated more than two-fold commonly in both cells detected by human expression microarray representing 4000 known genes. The protein expression levels of ZNF91, c-Fos, BTF3a, GATA-1, RGS2, NDRG2 and RUNX1 were increased with western blot in correspond to microarray results.
PDS-C as an effective component for hematopoiesis, play the role to enhance proliferation and differentiation of megakaryocytes, also up-regulated expression of proliferation, differentiation-related genes and proteins in vitro. Objective: To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gone expression profile of megakaryocytes. Methods: Bone marrow culture of colony forming assay of megakaryocytic progenitor cells (CFU-MK) was observed for the promoting proliferation mediated by PDS-C, and differentiation of megakaryocytic blasts caused by PDS-C was analyzed with flow cytometry in CHRF-288 and Meg-01 cells, as well as proliferation, differentiation-related genes expression profile and protein expression levels were detected by human gone expression microarray and western blot. Results: In response to PDS-C 10, 20 and 50 mg/L, CFU-MK from 10 human bone marrow samples was increased by 28.9± 2.7%, 41.0% ± 3.2% and 40.5% ± 2.6% over untreated control, respectively (P〈0.01, each). Flow cytometry analysis showed that PDS-C treated CHRF-288 cells and Meg-01 cells significantly increased in CD42b, CD41, TSP and CD36 positive ratio, respectively. PDS-C induced 29 genes up-regulated more than two-fold commonly in both cells detected by human expression microarray representing 4000 known genes. The protein expression levels of ZNF91, c-Fos, BTF3a, GATA-1, RGS2, NDRG2 and RUNX1 were increased with western blot in correspond to microarray results. Conclusion: PDS-C as an effective component for hematopoiesis, play the role to enhance proliferation and differentiation of megakaryocytes, also up-regulated expression of proliferation, differentiation-related genes and proteins in vitro. KEYWORDS panaxadiol saponins, megakaryocyte, gone expression profile, proliferation, differentiation Objective To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gene expression profile of megakaryocytes. Methods Bone marrow culture of colony forming assay of megakaryocytic progenitor cells (CFU-MK) was observed for the promoting proliferation mediated by PDS-C, and differentiation of megakaryocytic blasts caused by PDS-C was analyzed with flow cytometry in CHRF-288 and Meg-01 cells, as well as proliferation, differentiation-related genes expression profile and protein expression levels were detected by human gene expression microarray and western blot. Results In response to PDS-C 10, 20 and 50 mg/L, CFU-MK from 10 human bone marrow samples was increased by 28.9%±2.7%, 41.0%±3.2% and 40.5%±2.6% over untreated control, respectively ( P <0.01, each). Flow cytometry analysis showed that PDS-C treated CHRF-288 cells and Meg-01 cells significantly increased in CD42b, CD41, TSP and CD36 positive ratio, respectively. PDS-C induced 29 genes up-regulated more than two-fold commonly in both cells detected by human expression microarray representing 4000 known genes. The protein expression levels of ZNF91, c-Fos, BTF3a, GATA-1, RGS2, NDRG2 and RUNX1 were increased with western blot in correspond to microarray results. Conclusion PDS-C as an effective component for hematopoiesis, play the role to enhance proliferation and differentiation of megakaryocytes, also up-regulated expression of proliferation, differentiation-related genes and proteins in vitro . |
| Author | 温伟为 孙馨 庄海峰 林筱洁 郑智茵 高瑞兰 尹利明 |
| AuthorAffiliation | The Third People's Hospital of Hangzhou, Hangzhou (310009), China Department of Oncology, Zhejiang Provincial People's Hospital, Hangzhou (310014), China Institution of Hematology Research, the First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou (310006), China |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25917792$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1089_jir_2018_0037 crossref_primary_10_1007_s11655_019_3049_z crossref_primary_10_1007_s11655_017_2754_8 crossref_primary_10_1093_abbs_gmx062 crossref_primary_10_3390_ijms24043168 crossref_primary_10_1007_s11655_021_3283_z crossref_primary_10_12998_wjcc_v10_i14_4425 crossref_primary_10_1016_j_intimp_2023_110131 crossref_primary_10_1007_s11655_019_3031_9 crossref_primary_10_1039_D3FO03572G crossref_primary_10_1016_j_jep_2020_113581 crossref_primary_10_1080_13880209_2020_1844761 |
| Cites_doi | 10.1142/S0192415X09007211 10.4110/in.2011.11.6.348 10.1182/blood-2004-03-0940 10.1126/science.270.5235.467 10.1182/blood-2008-03-145722 10.1002/jcb.22142 10.1111/j.1745-7254.2007.00551.x 10.1007/s11655-012-1306-4 10.1016/j.devcel.2011.04.008 10.1371/journal.pone.0022649 |
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| Copyright | Chinese Association of the Integration of Traditional and Western Medicine and Springer-Verlag Berlin Heidelberg 2016 |
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| Notes | WEN Wei-wei , SUN Xin , ZHUANG Hai-feng ,LIN Xiao-jie, ZHENG Zhi-yin, GAO Rui-lan ,YIN Li-ming (1. The Third People's Hospital of Hangzhou, Hangzhou (310009), China; 2. Department of Oncology, Zhejiang Provincial People's Hospital, Hangzhou (310014), China; 3. Institution of Hematology Research, the First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou (310006), China ) Objective: To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and corresponding gone expression profile of megakaryocytes. Methods: Bone marrow culture of colony forming assay of megakaryocytic progenitor cells (CFU-MK) was observed for the promoting proliferation mediated by PDS-C, and differentiation of megakaryocytic blasts caused by PDS-C was analyzed with flow cytometry in CHRF-288 and Meg-01 cells, as well as proliferation, differentiation-related genes expression profile and protein expression levels were detected by human gone expression microarray and western blot. Results: In response to PDS-C 10, 20 and 50 mg/L, CFU-MK from 10 human bone marrow samples was increased by 28.9± 2.7%, 41.0% ± 3.2% and 40.5% ± 2.6% over untreated control, respectively (P〈0.01, each). Flow cytometry analysis showed that PDS-C treated CHRF-288 cells and Meg-01 cells significantly increased in CD42b, CD41, TSP and CD36 positive ratio, respectively. PDS-C induced 29 genes up-regulated more than two-fold commonly in both cells detected by human expression microarray representing 4000 known genes. The protein expression levels of ZNF91, c-Fos, BTF3a, GATA-1, RGS2, NDRG2 and RUNX1 were increased with western blot in correspond to microarray results. Conclusion: PDS-C as an effective component for hematopoiesis, play the role to enhance proliferation and differentiation of megakaryocytes, also up-regulated expression of proliferation, differentiation-related genes and proteins in vitro. KEYWORDS panaxadiol saponins, megakaryocyte, gone expression profile, proliferation, differentiation 11-4928/R panaxadiol saponins, megakaryocyte, gene expression profile, proliferation, differentiation |
| PMID | 25917792 |
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| Snippet | Objective: To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation,... Objective To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation... To investigate the effects of panaxadiol saponins component (PDS-C) isolated from total saponins of panax ginseng on proliferation, differentiation and... |
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| SubjectTerms | Blotting, Western Bone Marrow Cells - cytology Cell Differentiation - drug effects Cell Proliferation - drug effects Cells, Cultured Colony-Forming Units Assay Drugs, Chinese Herbal - pharmacology Flow Cytometry Gene Expression Profiling Ginsenosides - pharmacology Humans Medicine Medicine & Public Health Megakaryocytes - cytology Megakaryocytes - drug effects Megakaryocytes - metabolism Original Article Patents as Topic Saponins - pharmacology Stem Cells - cytology Stem Cells - drug effects Transcription Factors - metabolism Up-Regulation - drug effects Up-Regulation - genetics 人参二醇 人参总皂苷 体外分化 基因表达谱 巨核细胞 有效成分 流式细胞仪分析 细胞增殖 |
| Title | Effects of Panaxadiol Saponins Component as A New Chinese Patent Medicine on Proliferation, Differentiation and Corresponding Gene Expression Profile of Megakaryocytes |
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