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  1. Book ; Online ; E-Book: Perinatal stem cells

    Han, Zhong Chao / Takahashi, Tsuneo A. / Han, Zhibo / Li, Zongjin

    biology, manufacturing and translational medicine

    2019  

    Author's details Zhong Chao Han, Tsuneo A. Takahashi, Zhibo Han, Zongjin Li editors
    Language English
    Size 1 Online-Ressource (vi, 173 Seiten), Illustrationen
    Publisher Springer
    Publishing place Singapore
    Publishing country Singapore
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT020019201
    ISBN 978-981-13-2703-2 ; 9789811327025 ; 981-13-2703-3 ; 9811327025
    DOI 10.1007/978-981-13-2703-2
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Article: [Comparative Study of the Two High-Efficient Strategies for

    Wang, Ti-Er / Sun, Yun-Yan / Han, Zhong-Chao / Zhang, Lei-Sheng / Shi, Ming-Xia

    Zhongguo shi yan xue ye xue za zhi

    2023  Volume 31, Issue 2, Page(s) 553–561

    Abstract: Objective: To explore the similarities and variations of biological phenotype and cytotoxicity of human umbilical cord blood natural killer cells (hUC- NK) after human umbilical cord blood-derived mononuclear cells (hUC-MNC) activated and expanded by ... ...

    Abstract Objective: To explore the similarities and variations of biological phenotype and cytotoxicity of human umbilical cord blood natural killer cells (hUC- NK) after human umbilical cord blood-derived mononuclear cells (hUC-MNC) activated and expanded by two
    Methods: Umbilical cord blood mononuclear cells (MNC) from healthy donor were enriched by Ficoll-based density gradient centrifugation. Then, the phenotype, subpopulations, cell viability and cytotoxicity of NK cells derived from Miltenyi medium (denoted as M-NK) and X-VIVO 15 (denoted as X-NK) were compared using a "3IL" strategy.
    Results: After a 14-day's culture, the contents of CD3
    Conclusion: The two strategies were adequate for high-efficient generation of NK cells with high level of activation
    MeSH term(s) Humans ; Fetal Blood ; Killer Cells, Natural ; T-Lymphocytes ; Leukocytes, Mononuclear/metabolism ; Cell Proliferation ; CD56 Antigen/metabolism
    Chemical Substances CD56 Antigen
    Language Chinese
    Publishing date 2023-04-25
    Publishing country China
    Document type English Abstract ; Journal Article
    ZDB-ID 2404306-0
    ISSN 1009-2137
    ISSN 1009-2137
    DOI 10.19746/j.cnki.issn.1009-2137.2023.02.035
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Heterogeneity of Human Mesenchymal Stromal/Stem Cells.

    Wang, Weiqiang / Han, Zhong Chao

    Advances in experimental medicine and biology

    2019  Volume 1123, Page(s) 165–177

    Abstract: Increasing evidence has shown that mesenchymal stem cells (MSCs) isolated from body tissues are heterogeneous while being examined in vitro and in vivo. Besides some common characteristics, MSCs derived from different tissues exhibit unique biological ... ...

    Abstract Increasing evidence has shown that mesenchymal stem cells (MSCs) isolated from body tissues are heterogeneous while being examined in vitro and in vivo. Besides some common characteristics, MSCs derived from different tissues exhibit unique biological properties. In addition, the therapeutic effects of MSCs may vary widely due to their heterogeneity and the technical differences in large-scale ex vivo expansion. In this chapter, the heterogeneity of MSCs will be discussed in three levels: the individual donors, the tissue sources, and the cell surface markers.
    MeSH term(s) Bone Marrow Cells/cytology ; Cell Differentiation ; Humans ; Membrane Proteins ; Mesenchymal Stem Cells/cytology
    Chemical Substances Membrane Proteins
    Language English
    Publishing date 2019-04-23
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2214-8019 ; 0065-2598
    ISSN (online) 2214-8019
    ISSN 0065-2598
    DOI 10.1007/978-3-030-11096-3_10
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Therapeutic prospects of mesenchymal stem/stromal cells in COVID-19 associated pulmonary diseases: From bench to bedside.

    Zhang, Lei-Sheng / Yu, Yi / Yu, Hao / Han, Zhong-Chao

    World journal of stem cells

    2021  Volume 13, Issue 8, Page(s) 1058–1071

    Abstract: The ongoing outbreak of coronavirus disease 2019 (COVID-19) caused by the novel severe acute respiratory syndrome coronavirus 2 has become a sudden public emergency of international concern and seriously threatens millions of people's life health. Two ... ...

    Abstract The ongoing outbreak of coronavirus disease 2019 (COVID-19) caused by the novel severe acute respiratory syndrome coronavirus 2 has become a sudden public emergency of international concern and seriously threatens millions of people's life health. Two current studies have indicated a favorable role for mesenchymal stem/stromal cells (MSCs) in clinical remission of COVID-19 associated pulmonary diseases, yet the systematical elaboration of the therapeutics and underlying mechanism is far from satisfaction. In the present review, we summarize the therapeutic potential of MSCs in COVID-19 associated pulmonary diseases such as pneumonia induced acute lung injury, acute respiratory distress syndrome, and pulmonary fibrosis. Furthermore, we review the underlying mechanism of MSCs including direct- and trans-differentiation, autocrine and paracrine anti-inflammatory effects, homing, and neovascularization, as well as constitutive microenvironment. Finally, we discuss the prospects and supervision of MSC-based cytotherapy for COVID-19 management before large-scale application in clinical practice. Collectively, this review supplies overwhelming new references for understanding the landscapes of MSCs in the remission of COVID-19 associated pulmonary diseases.
    Language English
    Publishing date 2021-09-03
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2583482-4
    ISSN 1948-0210
    ISSN 1948-0210
    DOI 10.4252/wjsc.v13.i8.1058
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Clinical Efficacy of an Indwelling Transanal Tube for the Prevention of Anastomotic Leakage After Hirschsprung's Disease: A Single Center Experience with Chinese Patients.

    Wang, Yun-Jin / Han, Zhong-Chao / Chen, Liu / He, Yuan-Bin / Lin, Yu / Zhou, Chao-Ming

    Journal of laparoendoscopic & advanced surgical techniques. Part A

    2021  Volume 32, Issue 3, Page(s) 342–346

    Abstract: Background: ...

    Abstract Background:
    MeSH term(s) Anal Canal/surgery ; Anastomotic Leak/epidemiology ; Anastomotic Leak/etiology ; Anastomotic Leak/prevention & control ; Child ; China/epidemiology ; Digestive System Surgical Procedures/methods ; Hirschsprung Disease/surgery ; Humans ; Infant ; Postoperative Complications/prevention & control ; Retrospective Studies ; Treatment Outcome
    Language English
    Publishing date 2021-11-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1381909-4
    ISSN 1557-9034 ; 1092-6429
    ISSN (online) 1557-9034
    ISSN 1092-6429
    DOI 10.1089/lap.2021.0644
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Intravenously transplanted mesenchymal stromal cells: a new endocrine reservoir for cardioprotection.

    Huang, Anan / Liu, Yue / Qi, Xin / Chen, Shang / Huang, Haoyan / Zhang, Jun / Han, Zhibo / Han, Zhong-Chao / Li, Zongjin

    Stem cell research & therapy

    2022  Volume 13, Issue 1, Page(s) 253

    Abstract: Background: Intravenous administration of mesenchymal stromal cells (MSCs) has an acknowledged competence of cardiac repair, despite a lack of systematic description of the underlying biological mechanisms. The lung, but not the heart, is the main ... ...

    Abstract Background: Intravenous administration of mesenchymal stromal cells (MSCs) has an acknowledged competence of cardiac repair, despite a lack of systematic description of the underlying biological mechanisms. The lung, but not the heart, is the main trapped site for intravenously transplanted MSCs, which leaves a spatial gap between intravenously transplanted MSCs and the injured myocardium. How lung-trapped MSCs after intravenous transplantation rejuvenate the injured myocardium remains unknown.
    Methods: MSCs were isolated from human placenta tissue, and DF-MSCs or Gluc-MSCs were generated by transduced with firefly luciferase (Fluc)/enhanced green fluorescence protein (eGFP) or Gaussia luciferase (Gluc) lactadherin fusion protein. The therapeutic efficiency of intravenously transplanted MSCs was investigated in a murine model of doxorubicin (Dox)-induced cardiotoxicity. Trans-organ communication from the lung to the heart with the delivery of blood was investigated by testing the release of MSC-derived extracellular vesicles (MSC-EVs), and the potential miRNA inner MSC-EVs were screened out and verified. The potential therapeutic miRNA inner MSC-EVs were then upregulated or downregulated to assess the further therapeutic efficiency RESULTS: Dox-induced cardiotoxicity, characterized by cardiac atrophy, left ventricular dysfunction, and injured myocardium, was alleviated by consecutive doses of MSCs. These cardioprotective effects might be attributed to suppressing GRP78 triggering endoplasmic reticulum (ER) stress-induced apoptosis in cardiomyocytes. Our results confirmed that miR-181a-5p from MSCs-derived EVs (MSC-EVs) inhibited GRP78. Intravenous DF-MSCs were trapped in lung vasculature, secreted a certain number of EVs into serum, which could be confirmed by the detection of eGFP
    Conclusions: This study identifies intravenously transplanted MSCs, as an endocrine reservoir, to secrete cardioprotective EVs into blood continuously and gradually to confer the trans-organ communication that relieves Dox-induced cardiotoxicity.
    MeSH term(s) Animals ; Cardiotoxicity/therapy ; Disease Models, Animal ; Doxorubicin/pharmacology ; Extracellular Vesicles/metabolism ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stem Cells/metabolism ; Mice ; MicroRNAs/genetics ; MicroRNAs/metabolism
    Chemical Substances MicroRNAs ; Doxorubicin (80168379AG)
    Language English
    Publishing date 2022-06-17
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2548671-8
    ISSN 1757-6512 ; 1757-6512
    ISSN (online) 1757-6512
    ISSN 1757-6512
    DOI 10.1186/s13287-022-02922-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Genetically engineered mesenchymal stem cells as a nitric oxide reservoir for acute kidney injury therapy.

    Huang, Haoyan / Qian, Meng / Liu, Yue / Chen, Shang / Li, Huifang / Han, Zhibo / Han, Zhong-Chao / Chen, Xiang-Mei / Zhao, Qiang / Li, Zongjin

    eLife

    2023  Volume 12

    Abstract: Nitric oxide (NO), as a gaseous therapeutic agent, shows great potential for the treatment of many kinds of diseases. Although various NO delivery systems have emerged, the immunogenicity and long-term toxicity of artificial carriers hinder the potential ...

    Abstract Nitric oxide (NO), as a gaseous therapeutic agent, shows great potential for the treatment of many kinds of diseases. Although various NO delivery systems have emerged, the immunogenicity and long-term toxicity of artificial carriers hinder the potential clinical translation of these gas therapeutics. Mesenchymal stem cells (MSCs), with the capacities of self-renewal, differentiation, and low immunogenicity, have been used as living carriers. However, MSCs as gaseous signaling molecule (GSM) carriers have not been reported. In this study, human MSCs were genetically modified to produce mutant β-galactosidase (β-GAL
    MeSH term(s) Mice ; Animals ; Humans ; Nitric Oxide ; Mesenchymal Stem Cells ; Stem Cells ; Genetic Engineering ; Acute Kidney Injury/therapy
    Chemical Substances Nitric Oxide (31C4KY9ESH)
    Language English
    Publishing date 2023-09-11
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.84820
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Superior protective effects of PGE2 priming mesenchymal stem cells against LPS-induced acute lung injury (ALI) through macrophage immunomodulation.

    Hezam, Kamal / Wang, Chen / Fu, Enze / Zhou, Manqian / Liu, Yue / Wang, Hui / Zhu, Lihong / Han, Zhibo / Han, Zhong-Chao / Chang, Ying / Li, Zongjin

    Stem cell research & therapy

    2023  Volume 14, Issue 1, Page(s) 48

    Abstract: Background: Mesenchymal stem cells (MSCs) have demonstrated remarkable therapeutic promise for acute lung injury (ALI) and its severe form, acute respiratory distress syndrome (ARDS). MSC secretomes contain various immunoregulatory mediators that ... ...

    Abstract Background: Mesenchymal stem cells (MSCs) have demonstrated remarkable therapeutic promise for acute lung injury (ALI) and its severe form, acute respiratory distress syndrome (ARDS). MSC secretomes contain various immunoregulatory mediators that modulate both innate and adaptive immune responses. Priming MSCs has been widely considered to boost their therapeutic efficacy for a variety of diseases. Prostaglandin E2 (PGE2) plays a vital role in physiological processes that mediate the regeneration of injured organs.
    Methods: This work utilized PGE2 to prime MSCs and investigated their therapeutic potential in ALI models. MSCs were obtained from human placental tissue. MSCs were transduced with firefly luciferase (Fluc)/eGFP fusion protein for real-time monitoring of MSC migration. Comprehensive genomic analyses explored the therapeutic effects and molecular mechanisms of PGE2-primed MSCs in LPS-induced ALI models.
    Results: Our results demonstrated that PGE2-MSCs effectively ameliorated lung injury and decreased total cell numbers, neutrophils, macrophages, and protein levels in bronchoalveolar lavage fluid (BALF). Meanwhile, treating ALI mice with PGE2-MSCs dramatically reduced histopathological changes and proinflammatory cytokines while increasing anti-inflammatory cytokines. Furthermore, our findings supported that PGE2 priming improved the therapeutic efficacy of MSCs through M2 macrophage polarization.
    Conclusion: PGE2-MSC therapy significantly reduced the severity of LPS-induced ALI in mice by modulating macrophage polarization and cytokine production. This strategy boosts the therapeutic efficacy of MSCs in cell-based ALI therapy.
    MeSH term(s) Pregnancy ; Female ; Mice ; Humans ; Animals ; Lipopolysaccharides/toxicity ; Dinoprostone/metabolism ; Mesenchymal Stem Cell Transplantation/methods ; Placenta/metabolism ; Acute Lung Injury/chemically induced ; Acute Lung Injury/therapy ; Acute Lung Injury/metabolism ; Mesenchymal Stem Cells/metabolism ; Cytokines/metabolism ; Immunomodulation ; Macrophages/metabolism ; Immunity ; Lung/pathology
    Chemical Substances Lipopolysaccharides ; Dinoprostone (K7Q1JQR04M) ; Cytokines
    Language English
    Publishing date 2023-03-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2548671-8
    ISSN 1757-6512 ; 1757-6512
    ISSN (online) 1757-6512
    ISSN 1757-6512
    DOI 10.1186/s13287-023-03277-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Human umbilical cord-derived mesenchymal stem cells treatment for refractory uveitis: a case series.

    Yang, Jing / Ren, Xin-Jun / Chen, Xi-Teng / Jiang, Yuan-Feng / Han, Zhi-Bo / Han, Zhong-Chao / Li, Xiao-Rong / Zhang, Xiao-Min

    International journal of ophthalmology

    2021  Volume 14, Issue 11, Page(s) 1784–1790

    Abstract: Aim: To evaluate therapeutic outcomes of human umbilical cord-derived mesenchymal stem cells (HUC-MSCs) treatment in patients with refractory uveitis.: Methods: A retrospective and noncomparative review was performed on four patients with refractory ... ...

    Abstract Aim: To evaluate therapeutic outcomes of human umbilical cord-derived mesenchymal stem cells (HUC-MSCs) treatment in patients with refractory uveitis.
    Methods: A retrospective and noncomparative review was performed on four patients with refractory uveitis from December 2013 to December 2017. HUC-MSCs were administered intravenously at a dose of 1×10
    Results: All four patients presented with responses to HUC-MSCs treatment, with three males and one female. The numbers of uveitis attacks per year after the HUC-MSCs treatment (0, 2, 0, 0 respectively) all decreased compared with the numbers before the treatment (3, 6, 4, 4 respectively). The oral steroid and immunosuppressive agents were tapered in all patients without recrudescence of ocular inflammation, and three patients discontinued their oral medicine at the last visit. The best corrected visual acuity (BCVA) of 3 patients was improved to varying degrees, and the BCVA of 1 patient remained at 20/20 (Snellen chart) from the first to the last consultation.
    Conclusion: The study provides an effective therapy of HUC-MSCs in maintaining remission in patients affected by uveitis refractory to previous immunosuppressant treatments.
    Language English
    Publishing date 2021-11-18
    Publishing country China
    Document type Journal Article
    ZDB-ID 2663246-9
    ISSN 2227-4898 ; 2222-3959
    ISSN (online) 2227-4898
    ISSN 2222-3959
    DOI 10.18240/ijo.2021.11.20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: [Vascular differentiation of hematopoietic stem cells and possible application in the treatment of limb ischemic diseases].

    Han, Zhong-chao

    Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae

    2005  Volume 27, Issue 6, Page(s) 782–785

    Abstract: Hematopoietic stem cell (HSC) is the first discovered and well studied tissue stem cell. HSC transplantation has been successfully applied to cure a variety of diseases of hematological and immunological systems. It has long believed that HSC and ... ...

    Abstract Hematopoietic stem cell (HSC) is the first discovered and well studied tissue stem cell. HSC transplantation has been successfully applied to cure a variety of diseases of hematological and immunological systems. It has long believed that HSC and angioblast come from the common stem cell, the hemangioblast. Recently, HSC has been demonstrated to be able to differentiate into vascular endothelial cells. In animal in vivo models, HSC transplantation can promote angiogenesis and improve limb ischemia. Several pilot clinical studies have shown that transplantation of bone marrow and granulocyte colony stimulating factor mobilized peripheral blood HSC promoted vascular reconstitution in ischemic limbs. Umbilical cord blood has been an important source of HSC for clinical transplantation. Animal studies have demonstrated the efficiency of cord blood HSC transplantation in improving critical limb ischemia. These studies have provided evidences that HSC can be used for the treatment of vascular diseases.
    MeSH term(s) Animals ; Cell Differentiation ; Extremities/blood supply ; Hematopoietic Stem Cell Mobilization/methods ; Hematopoietic Stem Cell Transplantation/methods ; Hematopoietic Stem Cells/cytology ; Humans ; Ischemia/therapy
    Language Chinese
    Publishing date 2005-12
    Publishing country China
    Document type English Abstract ; Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 604853-5
    ISSN 1000-503X
    ISSN 1000-503X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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