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  1. Article ; Online: The piRNAs present in the developing testes of Chinese indigenous Xiang pigs.

    Ma, Xinrui / Niu, Xi / Huang, Shihui / Li, Sheng / Ran, Xueqin / Wang, Jiafu / Dai, Xinlan

    Theriogenology

    2022  Volume 189, Page(s) 92–106

    Abstract: ... tissues of animals and contributes to post-transcriptional regulation of genes. Xiang pigs present ... plays in the development of Xiang pigs is currently not understood. In this study, we sequenced and ... analyzed piRNAs expressed in the testes of Xiang pigs at four different ages, and identified endogenous ...

    Abstract The piRNA pathway plays an essential role in defense against transposable elements in the germline tissues of animals and contributes to post-transcriptional regulation of genes. Xiang pigs present an earlier sexual maturation compared with most European pig breeds, but the role that the piRNA pathway plays in the development of Xiang pigs is currently not understood. In this study, we sequenced and analyzed piRNAs expressed in the testes of Xiang pigs at four different ages, and identified endogenous piRNAs which were highly abundant at each time point. The lengths of the identified piRNAs ranged from 24 to 34 nucleotides (nt), with the most abundant length being 29 nt. Additionally, there was a strong bias for uracil at the first position, a slight bias for adenine at position 10 and frequent 5'-10 nt complementary sequences, suggesting that ping-pong-mediated silencing is present in the Xiang pig germline. We observed that the piRNA composition changed from TE-associated piRNAs in two- and three-month-old testes to predominantly gene-derived and intergenic piRNAs in six- and twelve-month-old testes, with a gradual increase in the expression level of piRNAs over the course of testis development. And more than half of piRNA reads mapped to just a few of 473 predicted piRNA clusters. Additionally, we found that several genes were highly enriched by piRNA reads, including CYP19A1, PRMT8, SUZ12, WWOX, SGSM1 and MIF. The functions of these genes are primarily associated with steroidogenesis and histone modification. Changes in piRNA composition and widespread expression patterns during spermatid development indicate that these small ncRNAs may be responsible not only for transposon suppression but also for post-transcriptional regulation of several protein-coding genes essential for normal spermatogenesis.
    MeSH term(s) Animals ; China ; DNA Transposable Elements/genetics ; Male ; RNA, Small Interfering/genetics ; Spermatogenesis/genetics ; Swine/genetics ; Testis/metabolism
    Chemical Substances DNA Transposable Elements ; RNA, Small Interfering
    Language English
    Publishing date 2022-06-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 189232-0
    ISSN 1879-3231 ; 0093-691X
    ISSN (online) 1879-3231
    ISSN 0093-691X
    DOI 10.1016/j.theriogenology.2022.05.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: The piRNAs present in the developing testes of Chinese indigenous Xiang pigs

    Ma, Xinrui / Niu, Xi / Huang, Shihui / Li, Sheng / Ran, Xueqin / Wang, Jiafu / Dai, Xinlan

    Theriogenology. 2022 Sept. 01, v. 189

    2022  

    Abstract: ... tissues of animals and contributes to post-transcriptional regulation of genes. Xiang pigs present ... plays in the development of Xiang pigs is currently not understood. In this study, we sequenced and ... analyzed piRNAs expressed in the testes of Xiang pigs at four different ages, and identified endogenous ...

    Abstract The piRNA pathway plays an essential role in defense against transposable elements in the germline tissues of animals and contributes to post-transcriptional regulation of genes. Xiang pigs present an earlier sexual maturation compared with most European pig breeds, but the role that the piRNA pathway plays in the development of Xiang pigs is currently not understood. In this study, we sequenced and analyzed piRNAs expressed in the testes of Xiang pigs at four different ages, and identified endogenous piRNAs which were highly abundant at each time point. The lengths of the identified piRNAs ranged from 24 to 34 nucleotides (nt), with the most abundant length being 29 nt. Additionally, there was a strong bias for uracil at the first position, a slight bias for adenine at position 10 and frequent 5′-10 nt complementary sequences, suggesting that ping-pong-mediated silencing is present in the Xiang pig germline. We observed that the piRNA composition changed from TE-associated piRNAs in two- and three-month-old testes to predominantly gene-derived and intergenic piRNAs in six- and twelve-month-old testes, with a gradual increase in the expression level of piRNAs over the course of testis development. And more than half of piRNA reads mapped to just a few of 473 predicted piRNA clusters. Additionally, we found that several genes were highly enriched by piRNA reads, including CYP19A1, PRMT8, SUZ12, WWOX, SGSM1 and MIF. The functions of these genes are primarily associated with steroidogenesis and histone modification. Changes in piRNA composition and widespread expression patterns during spermatid development indicate that these small ncRNAs may be responsible not only for transposon suppression but also for post-transcriptional regulation of several protein-coding genes essential for normal spermatogenesis.
    Keywords adenine ; animal reproduction ; germ cells ; histone code ; nucleotides ; sexual maturity ; spermatogenesis ; steroidogenesis ; swine ; testes ; transposons ; type I protein arginine methyltransferase ; uracil
    Language English
    Dates of publication 2022-0901
    Size p. 92-106.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 189232-0
    ISSN 1879-3231 ; 0093-691X
    ISSN (online) 1879-3231
    ISSN 0093-691X
    DOI 10.1016/j.theriogenology.2022.05.028
    Database NAL-Catalogue (AGRICOLA)

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  3. Article: A Comprehensive Analysis of the Myocardial Transcriptome in ZBED6-Knockout Bama Xiang Pigs

    Wang, Shengnan / Tian, Wenjie / Pan, Dengke / Liu, Ling / Xu, Cheng / Ma, Yuehui / Wang, Dandan / Jiang, Lin

    Genes. 2022 Aug. 01, v. 13, no. 8

    2022  

    Abstract: ... of mRNAs and lncRNAs in myocardial tissue obtained from Bama Xiang pigs in the ZBED6 knockout group (ZBED6 ...

    Abstract The ZBED6 gene is a transcription factor that regulates the expression of IGF2 and affects muscle growth and development. However, its effect on the growth and development of the heart is still unknown. Emerging evidence suggests that long noncoding RNAs (lncRNAs) can regulate genes at the epigenetic, transcriptional, and posttranscriptional levels and play an important role in the development of eukaryotes. To investigate the function of ZBED6 in the cardiac development of pigs, we constructed the expression profiles of mRNAs and lncRNAs in myocardial tissue obtained from Bama Xiang pigs in the ZBED6 knockout group (ZBED6-KO) and the wild-type group (ZBED6-WT). A total of 248 differentially expressed genes (DEGs) and 209 differentially expressed lncRNAs (DELs) were detected, and 105 potential cis target genes of DELs were identified. The functional annotation analysis based on the Gene Ontology (GO) and Kyoto Encyclopaedia of Genes and Genomes (KEGG) databases revealed two GO items related to muscle development by the cis target genes of DELs. Moreover, IGF2 was the direct target gene of ZBED6 by ChIP-PCR experiment. Our results explored the mechanism and expression profile of mRNAs and lncRNAs of ZBED6 gene knockout on myocardium tissue development, mining the key candidate genes in that process like IGF2.
    Keywords epigenetics ; eukaryotic cells ; gene expression regulation ; gene ontology ; gene targeting ; genes ; growth and development ; muscle development ; muscles ; myocardium ; transcription (genetics) ; transcription factors ; transcriptome
    Language English
    Dates of publication 2022-0801
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2527218-4
    ISSN 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes13081382
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Mu-Xiang-You-Fang protects PC12 cells against OGD/R-induced autophagy via the AMPK/mTOR signaling pathway.

    Ma, Hui-Xia / Hou, Fan / Chen, Ai-Ling / Li, Ting-Ting / Zhu, Ya-Fei / Zhao, Qi-Peng

    Journal of ethnopharmacology

    2020  Volume 252, Page(s) 112583

    Abstract: Ethnopharmacological relevance: Mu-Xiang-You-Fang (MXYF) is a classic prescription of Hui medicine ...

    Abstract Ethnopharmacological relevance: Mu-Xiang-You-Fang (MXYF) is a classic prescription of Hui medicine. It is composed of five herbs and has been used to treat ischemic stroke for many years. However, the potential pharmacological mechanisms of MXYF remain unclear. The present research is aimed to investigate the protective effect and possible mechanisms of MXYF treatment in an in vitro model of cerebral ischemia-reperfusion injury.
    Materials and methods: An oxygen-glucose deprivation and reperfusion (OGD/R) model of PC12 cells was established. The effect of MXYF on the cell viability after OGD/R injury was determined using a cell counting kit (CCK-8) assay. The colorimetric method was used to determine the lactate dehydrogenase (LDH) leakage rate. The calcium concentration was determined by the chemical fluorescence method, and mitochondrial membrane potential was determined using flow cytometry. Monodansylcadaverine (MDC) staining and electron microscopic analysis were then conducted to detect autophagy after oxygen-glucose deprivation and reperfusion in PC12 cells. Immunofluorescence and western blot analyses were used to detect the expression of proteins associated with autophagy.
    Results: It was found that MXYF (1, 2, 4 μg/mL) could significantly increase cell viability and mitochondrial membrane potential and decrease the calcium concentration and LDH release rate in PC12 cells. After OGD/R injury in PC12 cells, the number of autophagosomes and autophagolysosome significantly increased. MXYF (4 μg/mL) inhibited the autophagy induced by OGD/R and inhibited the expression of LC3, beclin1, p-AMPK, and ULK1. In contrast, the expression of p-mTOR, p-p70s6k, and p62 was significantly enhanced.
    Conclusions: These findings suggest that MXYF inhibits autophagy after OGD/R-induced PC12 cell injury through the AMPK-mTOR pathway. Thus, MXYF might have therapeutic potential in treating ischemic stroke.
    MeSH term(s) AMP-Activated Protein Kinases/metabolism ; Animals ; Autophagy/drug effects ; Cell Hypoxia ; Drugs, Chinese Herbal/pharmacology ; Glucose/deficiency ; Neuroprotective Agents/pharmacology ; Oxygen ; PC12 Cells ; Rats ; Reperfusion Injury/drug therapy ; Reperfusion Injury/metabolism ; Signal Transduction/drug effects ; TOR Serine-Threonine Kinases/metabolism
    Chemical Substances Drugs, Chinese Herbal ; Mu-Xiang-You-Fang ; Neuroprotective Agents ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; mTOR protein, rat (EC 2.7.1.1) ; AMP-Activated Protein Kinases (EC 2.7.11.31) ; Glucose (IY9XDZ35W2) ; Oxygen (S88TT14065)
    Language English
    Publishing date 2020-01-22
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2020.112583
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Mu-Xiang-You-Fang protects PC12 cells against OGD/R-induced autophagy via the AMPK/mTOR signaling pathway

    Ma, Hui-xia / Chen, Ai-ling / Hou, Fan / Li, Ting-ting / Zhao, Qi-peng / Zhu, Ya-fei

    Journal of ethnopharmacology. 2020 Apr. 24, v. 252

    2020  

    Abstract: Mu-Xiang-You-Fang (MXYF) is a classic prescription of Hui medicine. It is composed of five herbs ...

    Abstract Mu-Xiang-You-Fang (MXYF) is a classic prescription of Hui medicine. It is composed of five herbs and has been used to treat ischemic stroke for many years. However, the potential pharmacological mechanisms of MXYF remain unclear. The present research is aimed to investigate the protective effect and possible mechanisms of MXYF treatment in an in vitro model of cerebral ischemia-reperfusion injury.An oxygen-glucose deprivation and reperfusion (OGD/R) model of PC12 cells was established. The effect of MXYF on the cell viability after OGD/R injury was determined using a cell counting kit (CCK-8) assay. The colorimetric method was used to determine the lactate dehydrogenase (LDH) leakage rate. The calcium concentration was determined by the chemical fluorescence method, and mitochondrial membrane potential was determined using flow cytometry. Monodansylcadaverine (MDC) staining and electron microscopic analysis were then conducted to detect autophagy after oxygen-glucose deprivation and reperfusion in PC12 cells. Immunofluorescence and western blot analyses were used to detect the expression of proteins associated with autophagy.It was found that MXYF (1, 2, 4 μg/mL) could significantly increase cell viability and mitochondrial membrane potential and decrease the calcium concentration and LDH release rate in PC12 cells. After OGD/R injury in PC12 cells, the number of autophagosomes and autophagolysosome significantly increased. MXYF (4 μg/mL) inhibited the autophagy induced by OGD/R and inhibited the expression of LC3, beclin1, p-AMPK, and ULK1. In contrast, the expression of p-mTOR, p-p70s6k, and p62 was significantly enhanced.These findings suggest that MXYF inhibits autophagy after OGD/R-induced PC12 cell injury through the AMPK-mTOR pathway. Thus, MXYF might have therapeutic potential in treating ischemic stroke.
    Keywords autophagy ; calcium ; cell viability ; colorimetry ; electron microscopy ; flow cytometry ; fluorescence ; fluorescent antibody technique ; herbs ; lactate dehydrogenase ; membrane potential ; mitochondrial membrane ; models ; protective effect ; proteins ; signal transduction ; staining ; stroke ; therapeutics ; traditional medicine ; Western blotting
    Language English
    Dates of publication 2020-0424
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2020.112583
    Database NAL-Catalogue (AGRICOLA)

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  6. Article ; Online: Neuroprotective effect and mechanism of Mu-Xiang-You-Fang on cerebral ischemia-reperfusion injury in rats.

    Zhao, Qipeng / Cheng, Xiuli / Wang, Xiaobo / Wang, Jing / Zhu, Yafei / Ma, Xueqin

    Journal of ethnopharmacology

    2016  Volume 192, Page(s) 140–147

    Abstract: ... of Mu-Xiang-You-Fang (MXYF), a classic Traditional Chinese Medicine used by Chinese minorities to treat ...

    Abstract Ethnopharmacological relevance: The present study is to investigate the neuroprotective effect of Mu-Xiang-You-Fang (MXYF), a classic Traditional Chinese Medicine used by Chinese minorities to treat stroke, on cerebral ischemia-reperfusion (I/R) injury and the related signaling pathways.
    Materials and methods: Male Sprague-Dawley rats were divided into 6 groups: sham group, I/R group, nimodipine and MXYF (58, 116 and 232mg/kg respectively) groups. Cerebral ischemia model was induced by middle cerebral artery occlusion for 2h followed by reperfusion for 48h. Neurological functional score was evaluated according to the method of Zea longa's score and the infarct area was determined by 2,3,5-triphenyltetrazolium chloride (TTC) staining at 48h after reperfusion. The protein expression of cytochrome c (cyt-c), Bcl-2, Bax, caspase-9, caspase-3 and caspase-7 were analyzed by western blot and the mRNA expression of Caspase-9, Caspase-3 and Caspase-7 were determined by the reverse transcription-polymerase chain reaction.
    Results: Oral administration of MXYF (116 and 232mg/kg) significantly reduced the neurological functional score and attenuated the cerebral infarct area. Western blot analysis showed that the expression of Bcl-2 is enhanced and Bax expression is inhibited after treatment with MXYF (116 and 232mg/kg), leading to significant increase of the ratio between Bcl-2 and Bax. Furthermore, the protein expression of cyt-c, caspase-9, caspase-3 and caspase-7 was significantly inhibited while the mRNA expression of caspase-9, caspase-3 and caspase-7 but not cyt-c was markedly inhibited in the MXYF (116 and 232mg/kg) treatment groups compared with the I/R group.
    Conclusions: The above data suggested that MXYF has potential neuroprotective activities by the regulation of apoptotic pathway, MXYF is a promising agent in treatment of stroke.
    MeSH term(s) Animals ; Apoptosis/drug effects ; Apoptosis Regulatory Proteins/genetics ; Apoptosis Regulatory Proteins/metabolism ; Behavior, Animal/drug effects ; Brain/drug effects ; Brain/metabolism ; Brain/pathology ; Brain/physiopathology ; Cytoprotection ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Drugs, Chinese Herbal/pharmacology ; Gas Chromatography-Mass Spectrometry ; Gene Expression Regulation ; Infarction, Middle Cerebral Artery/drug therapy ; Infarction, Middle Cerebral Artery/genetics ; Infarction, Middle Cerebral Artery/metabolism ; Infarction, Middle Cerebral Artery/pathology ; Male ; Neuroprotective Agents/isolation & purification ; Neuroprotective Agents/pharmacology ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Rats, Sprague-Dawley ; Reperfusion Injury/genetics ; Reperfusion Injury/metabolism ; Reperfusion Injury/pathology ; Reperfusion Injury/prevention & control ; Signal Transduction/drug effects
    Chemical Substances Apoptosis Regulatory Proteins ; Drugs, Chinese Herbal ; Mu-Xiang-You-Fang ; Neuroprotective Agents ; RNA, Messenger
    Language English
    Publishing date 2016-11-04
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2016.07.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Book ; Audio / Video: Xiang shuo jiu shuo

    Ma, Jianfei / Mao, Yue

    han yu kou yu wan quan shou ce = Say it now : a complete handbook of spoken chinese

    2007  

    Author's details Jianfei Ma; Mao Yue
    Language Chinese
    Size MP3 CD-Rom
    Publisher Beijing yu yan da xue chu ban she
    Publishing place Beijing
    Document type Book ; Audio / Video
    ISBN 9787561918227 ; 7561918224
    Database Former special subject collection: coastal and deep sea fishing

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  8. Article: Neuroprotective effect and mechanism of Mu-Xiang-You-Fang on cerebral ischemia-reperfusion injury in rats

    Zhao, Qipeng / Jing Wang / Xiaobo Wang / Xiuli Cheng / Xueqin Ma / Yafei Zhu

    Journal of ethnopharmacology. 2016 Nov. 04, v. 192

    2016  

    Abstract: The present study is to investigate the neuroprotective effect of Mu-Xiang-You-Fang (MXYF ...

    Abstract The present study is to investigate the neuroprotective effect of Mu-Xiang-You-Fang (MXYF), a classic Traditional Chinese Medicine used by Chinese minorities to treat stroke, on cerebral ischemia-reperfusion (I/R) injury and the related signaling pathways.Male Sprague-Dawley rats were divided into 6 groups: sham group, I/R group, nimodipine and MXYF (58, 116 and 232mg/kg respectively) groups. Cerebral ischemia model was induced by middle cerebral artery occlusion for 2h followed by reperfusion for 48h. Neurological functional score was evaluated according to the method of Zea longa’s score and the infarct area was determined by 2,3,5-triphenyltetrazolium chloride (TTC) staining at 48h after reperfusion. The protein expression of cytochrome c (cyt-c), Bcl-2, Bax, caspase-9, caspase-3 and caspase-7 were analyzed by western blot and the mRNA expression of Caspase-9, Caspase-3 and Caspase-7 were determined by the reverse transcription-polymerase chain reaction.Oral administration of MXYF (116 and 232mg/kg) significantly reduced the neurological functional score and attenuated the cerebral infarct area. Western blot analysis showed that the expression of Bcl-2 is enhanced and Bax expression is inhibited after treatment with MXYF (116 and 232mg/kg), leading to significant increase of the ratio between Bcl-2 and Bax. Furthermore, the protein expression of cyt-c, caspase-9, caspase-3 and caspase-7 was significantly inhibited while the mRNA expression of caspase-9, caspase-3 and caspase-7 but not cyt-c was markedly inhibited in the MXYF (116 and 232mg/kg) treatment groups compared with the I/R group.The above data suggested that MXYF has potential neuroprotective activities by the regulation of apoptotic pathway, MXYF is a promising agent in treatment of stroke.
    Keywords 2,3,5-triphenyltetrazolium chloride ; apoptosis ; caspase-3 ; caspase-7 ; caspase-9 ; cytochrome c ; gene expression ; infarction ; ischemia ; messenger RNA ; models ; neuroprotective effect ; Oriental traditional medicine ; protein synthesis ; rats ; staining ; stroke ; Western blotting
    Language English
    Dates of publication 2016-1104
    Size p. 140-147.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2016.07.016
    Database NAL-Catalogue (AGRICOLA)

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  9. Book: Xiang qi miao sha - Mou lüe pian

    Ma, Ge / Wang, Xiaping

    (Kan gu shi xue xiang qi cong shu ; 看故事学象棋丛书)

    2009  

    Author's details Ma Ge ; Wang Xiaping
    Series title Kan gu shi xue xiang qi cong shu
    看故事学象棋丛书
    Keywords Chinesisches Schach
    Language Chinese
    Size getrennte Zählung, graph. Darst.
    Edition 1. Auflage
    Publisher Jiangsu ke xue ji shu chu ban she
    Publishing place Nanjing
    Document type Book
    ISBN 9787534569548 ; 7534569540
    Database Former special subject collection: coastal and deep sea fishing

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  10. Book: Shanghai fei wu zhi wen hua yi chan chuan tong yi yao xiang mu feng cai

    Ma, Junjian

    2014  

    Author's details Ma Junjian zhu bian
    MeSH term(s) Medicine, Chinese Traditional ; Materia Medica
    Keywords China
    Language Chinese
    Size 130 p. :, ill., ports.
    Edition Di 1 ban.
    Publisher Shanghai ke xue ji shu chu ban she
    Publishing place Shanghai
    Document type Book
    ISBN 9787547821503 ; 7547821502
    Database Catalogue of the US National Library of Medicine (NLM)

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