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  1. AU="Mo, Jinping"
  2. AU="Lui, Wen"
  3. AU="Strati, V."
  4. AU="Dixon, Matthew W.A"
  5. AU=da Mata Kanzaki Elida C G
  6. AU="ElenaTourkina"
  7. AU="Chu, Yaojuan"
  8. AU="Bakker, Michiel A."
  9. AU=Hill W Cary AU=Hill W Cary
  10. AU="Hand, Marissa"
  11. AU="Guerra, Giselle"
  12. AU="Allouch, Asma"

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  1. Artikel ; Online: Advanced-platelet-rich fibrin extract promotes adipogenic and osteogenic differentiation of human adipose-derived stem cells in a dose-dependent manner in vitro.

    Liang, Zhijie / Huang, Donglin / Nong, Wenhai / Mo, Jinping / Zhu, Dandan / Wang, Mengxin / Chen, Maojian / Wei, Changyuan / Li, Hongmian

    Tissue & cell

    2021  Band 71, Seite(n) 101506

    Abstract: Advanced platelet-rich fibrin (A-PRF) is an autogenous biological material obtained from peripheral blood. A-PRF extract (A-PRFe) contains a high concentration of various cytokines that are increasingly appreciated for their roles in improving stem cell ... ...

    Abstract Advanced platelet-rich fibrin (A-PRF) is an autogenous biological material obtained from peripheral blood. A-PRF extract (A-PRFe) contains a high concentration of various cytokines that are increasingly appreciated for their roles in improving stem cell repairing function during tissue regeneration. However, the optimal A-PRFe concentration to stimulate stem cells is unknown. This study aimed to identify the optimal concentrations of A-PRFe to promote adipogenic and osteogenic differentiation of human adipose-derived stem cells (ASCs). We produced A-PRFe from A-PRF clots by centrifuging fresh peripheral blood samples and isolated and identified ASCs using surface CD markers and multilineage differentiation potential. Enzyme-linked immunosorbent assay (ELISA) showed the concentrations of several cytokines, including b-FGF, PDGF-BB, and others, increased gradually, peaked on day 7 and then decreased. Cell proliferation assays showed A-PRFe significantly stimulated ASC proliferation, and proliferation significantly increased at higher A-PRFe doses. The degree of adipogenic and osteogenic differentiation increased at higher A-PRFe concentrations in the culture medium, as determined by oil red O and alizarin red staining. Reverse transcription polymerase chain reaction (RT-PCR) showed that expression levels of genes related to adipogenic/osteogenic differentiation (PPARγ2, C/EBPα, FABP4, Adiponectin, and ALP, OPN, OCN, RUNX2), paracrine (HIF-1α, VEGF, IGF-2) and immunoregulation (HSP70, IL-8) function were higher in groups with a higher concentration of A-PRFe than in lower concentration groups. This study demonstrates that A-PRFe is ideal for use in ASC applications in regenerative medicine because it improves biological functions, including proliferation, adipogenic/osteogenic differentiation, and paracrine function in a dose-dependent manner.
    Mesh-Begriff(e) Adipogenesis/drug effects ; Cell Differentiation/drug effects ; Complex Mixtures/chemistry ; Complex Mixtures/pharmacology ; Dose-Response Relationship, Drug ; Humans ; Mesenchymal Stem Cells/metabolism ; Osteogenesis/drug effects ; Platelet-Rich Fibrin/chemistry
    Chemische Substanzen Complex Mixtures
    Sprache Englisch
    Erscheinungsdatum 2021-02-05
    Erscheinungsland Scotland
    Dokumenttyp Journal Article
    ZDB-ID 204424-9
    ISSN 1532-3072 ; 0040-8166
    ISSN (online) 1532-3072
    ISSN 0040-8166
    DOI 10.1016/j.tice.2021.101506
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: The J bs-5YP peptide can alleviate dementia in senile mice by restoring the transcription of Slc40a1 to secrete the excessive iron from brain.

    Zou, Zhenyou / Wu, Fengyao / Chen, Liguan / Yao, Hua / Wang, Zengxian / Chen, Yongfeng / Qi, Ming / Jiang, Yang / Tang, Longhua / Gan, Xinying / Kong, Lingjia / Yang, Zhicheng / Huang, Xiaolan / Shu, Wei / Li, Bixue / Tan, Xinyu / Huang, Liwen / Bai, Shi / Wu, Lijuan /
    Mo, Jinping / Hu, Huilin / Liu, Huihua / Zou, Ruyi / Wei, Yuhua

    Journal of advanced research

    2024  

    Abstract: Introduction: With age and ATP decrease in the body, the transcription factors hypophosphorylation weakens the transcription of Slc40a1 and hinders the expression of the iron discharger ferroportin. This may lead to iron accumulation in the brain and ... ...

    Abstract Introduction: With age and ATP decrease in the body, the transcription factors hypophosphorylation weakens the transcription of Slc40a1 and hinders the expression of the iron discharger ferroportin. This may lead to iron accumulation in the brain and the catalysis of free radicals that damage cerebral neurons and eventually lead to Alzheimer's disease (AD).
    Objectives: To prevent AD caused by brain iron excretion disorders and reveal the mechanism of J bs-5YP peptide restoring ferroportin.
    Methods: We prepared J bs-YP peptide and administered it to the senile mice with dementia. Then, the intelligence of the mice was tested using a Morris Water Maze. The ATP content in the body was detected using the ATP hydrophysis and Phosphate precipitation method. The activation of Slc40a1 transcription was assayed with ATAC seq and the ferroportin, as well as the phosphorylation levels of Ets1 in brain were detected by Western Blot.
    Results: The phosphorylation level of Ets1in brain was enhanced, and subsequently, the transcription of Slc40a1 was activated and ferroportin was increased in the brain, the levels of iron and free radicals were reduced, with the neurons protection, and the dementia was ultimately alleviated in the senile mice.
    Conclusion: J bs-5YP can recover the expression of ferroportin to excrete excessive iron in the brain of senile mice with dementia by enhancing the transcription of Slc40a1 via phosphorylating Ets1, revealing the potential of J bs-5YP as a drug to alleviate senile dementia.
    Sprache Englisch
    Erscheinungsdatum 2024-03-23
    Erscheinungsland Egypt
    Dokumenttyp Journal Article
    ZDB-ID 2541849-X
    ISSN 2090-1224 ; 2090-1224
    ISSN (online) 2090-1224
    ISSN 2090-1224
    DOI 10.1016/j.jare.2024.03.014
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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