Author: tcnhat

  • Embryonic Stem Cells – Recent Advances in Pluripotent Stem Cell-Based Regenerative Medicine

    Embryonic Stem Cells – Recent Advances in Pluripotent Stem Cell-Based Regenerative Medicine

     embryonic stem cell
    Edited by: Craig Atwood

    ISBN 978-953-307-198-5, Hard cover, 410 pages
    Publisher: InTech
    Publication date: April 2011
    Subject: Stem Cells

    Pluripotent stem cells have the potential to revolutionise medicine, providing treatment options for a wide range of diseases and conditions that currently lack therapies or cures. This book describes recent advances in the generation of tissue specific cell types for regenerative applications, as well as the obstacles that need to be overcome in order to recognize the potential of these cells.

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  • Embryonic Stem Cells – Basic Biology to Bioengineering

    Embryonic Stem Cells – Basic Biology to Bioengineering

    embryonic stem cell
    Edited by: Michael S. Kallos
    ISBN 978-953-307-278-4, Hard cover, 478 pages
    Publisher: InTech
    Publication date: September 2011
    Subject: Stem Cells

    Embryonic stem cells are one of the key building blocks of the emerging multidisciplinary field of regenerative medicine, and discoveries and new technology related to embryonic stem cells are being made at an ever increasing rate. This book provides a snapshot of some of the research occurring across a wide range of areas related to embryonic stem cells, including new methods, tools and technologies; new understandings about the molecular biology and pluripotency of these cells; as well as new uses for and sources of embryonic stem cells. The book will serve as a valuable resource for engineers, scientists, and clinicians as well as students in a wide range of disciplines.

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  • Embryonic Stem Cells – Differentiation and Pluripotent Alternatives

    Embryonic Stem Cells – Differentiation and Pluripotent Alternatives

    embryonic stem cellEdited by: Michael S. Kallos

    ISBN 978-953-307-632-4, Hard cover, 506 pages
    Publisher: InTech
    Publication date: October 2011
    Subject: Stem Cells

    The ultimate clinical implementation of embryonic stem cells will require methods and protocols to turn these unspecialized cells into the fully functioning cell types found in a wide variety of tissues and organs. In order to achieve this, it is necessary to clearly understand the signals and cues that direct embryonic stem cell differentiation. This book provides a snapshot of current research on the differentiation of embryonic stem cells to a wide variety of cell types, including neural, cardiac, endothelial, osteogenic, and hepatic cells. In addition, induced pluripotent stem cells and other pluripotent stem cell sources are described. The book will serve as a valuable resource for engineers, scientists, and clinicians as well as students in a wide range of disciplines.

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  • Stem Cells in Clinic and Research

    Stem Cells in Clinic and Research

     stem cell technologiesEdited by: Ali Gholamrezanezhad

    ISBN 978-953-307-797-0, Hard cover, 804 pages
    Publisher: InTech
    Publication date: August 2011
    Subject: Stem Cells

    Based on our current understanding of cell biology and strong supporting evidence from previous experiences, different types of human stem cell populations are capable of undergoing differentiation or trans-differentiation into functionally and biologically active cells for use in therapeutic purposes. So far, progress regarding the use of both in vitro and in vivo regenerative medicine models already offers hope for the application of different types of stem cells as a powerful new therapeutic option to treat different diseases that were previously considered to be untreatable. Remarkable achievements in cell biology resulting in the isolation and characterization of various stem cells and progenitor cells has increased the expectation for the development of a new approach to the treatment of genetic and developmental human diseases. Due to the fact that currently stem cells and umbilical cord banks are so strictly defined and available, it seems that this mission is investigationally more practical than in the past. On the other hand, studies performed on stem cells, targeting their conversion into functionally mature tissue, are not necessarily seeking to result in the clinical application of the differentiated cells; In fact, still one of the important goals of these studies is to get acquainted with the natural process of development of mature cells from their immature progenitors during the embryonic period onwards, which can produce valuable results as knowledge of the developmental processes during embryogenesis. For example, the cellular and molecular mechanisms leading to mature and adult cells developmental abnormalities are relatively unknown. This lack of understanding stems from the lack of a good model system to study cell development and differentiation. Hence, the knowledge reached through these studies can prove to be a breakthrough in preventing developmental disorders. Meanwhile, many researchers conduct these studies to understand the molecular and cellular basis of cancer development. The fact that cancer is one of the leading causes of death throughout the world, highlights the importance of these researches in the fields of biology and medicine.

     

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  • Research on in vitro culture and inducing nacre crystal formation of freshwater pearl mussel…

    Pham Van Phuc, Pham Quoc Viet, Nguyen Minh Hoang, Nguyen Thanh Tam and Phan Kim Ngoc (2011). Research on in vitro culture and inducing nacre crystal formation of freshwater pearl mussel mantle epithelial cell Sinohyriopsis cumingii. International Journal of Fisheries and Aquaculture 3(6):104- 112.

    International Journal of Fisheries and Aquaculture Vol. 3(6), pp.105- 113, June 2011

    ISSN 2006-9839 ©2011 Academic Journals

     

    Full Length Research Paper

     

    Research on in vitro culture and inducing nacre crystal formation of freshwater pearl mussel mantle epithelial cell Sinohyriopsis cumingii

    Pham Van Phuc*, Pham Quoc Viet, Nguyen Minh Hoang, Nguyen Thanh Tam and Phan Kim Ngoc

     

    Laboratory of Stem Cell Research and Application University of Science, Vietnam National University, Ho Chi Minh, Vietnam.

     

    *Corresponding author: E-mail: pvphuc@hcmuns.edu.vn.

     

    Accepted 28 March, 2011

    Abstract

    The foundation of natural pearl formation by mussels is calcium carbonate in the form of aragonite crystals, secreted essentially by the epithelial cells of mantle tissue as nacre. The in vitro explant culture of nacre secreting pallial mantle explants of freshwater pearl mussel was a vital step in the approach to the establishment of quality of pearl mussel species, by screening pearl mussel species that are able to form pearls with high efficiency. Moreover, the results of this research provide knowledge for the future in vitro colored pearl production. The aims of this research were to culture freshwater pearl mussel mantle epithelial cells and to investigate the capacity of their nacre-secretion when they were induced by some specific factors such as Ca2+, FGF-2 and EGF. In this research, mantle epithelial cells were cultured in four different kinds of medium (DMEM/F12, L15-M199, IMDM, TCM) and temperature [(4, 24°C and room temperature (28°C)] to select the suitable environment for pearl mussel mantle epithelial cell culture for at least one month. After that, old medium was changed by fresh medium supplemented with three inducers (Ca2+, FGF, EGF). Nacre secretion of these cells was evaluated via the nacre formation in culture medium. The results showed that the mantle epithelial cells may be cultured in vitro and secrete nacre in DMEM/F12 medium supplemented with 10% FBS, but the efficiency of secretion was independent with different inducers investigated. DMEM/F12 medium is the best for growing of mantle epithelial cells while IMDM medium is suitable for heamocyte –like cells.

    Key words: DMEM/F12, Ca2+, EGF, FGF, Freshwater mussel, mantle epithelial cells, nacre secretion.

  • Regeneration of Pancreatic B Cells of Type 1 Diabetic Mouse by Stem Cell Transplatation

    Pham Van Phuc, Pham Le Buu Truc, Duong Thanh Thuy, Truong Hai Nhung and Doan Chinh Chung, Phan Kim Ngoc. Regeneration of Pancreatic B Cells of Type 1 Diabetic Mouse by Stem Cell Transplatation. IFMBE Proceedings, 1, Volume 27, The Third International Conference on the Development of Biomedical Engineering in Vietnam, Part 5, Pages 163-166.

    IFMBE Proceedings, 2010, Volume 27, Part 5, 163-166, DOI: 10.1007/978-3-642-12020-6_40

    Regeneration of Pancreatic B Cells of Type 1 Diabetic Mouse by Stem Cell Transplatation

    Pham Van Phuc, Pham Le Buu Truc, Duong Thanh Thuy, Truong Hai Nhung, Doan Chinh Chung, Nguyen Khac Toan, Ma Kien Phuc and Phan Kim Ngoc

    Abstract

    Type 1 diabetes is the result of an autoimmune attack against the insulin-producing β cells of the pancreas. Current treatment for patients with type 1 diabetes typically involves a rigorous and invasive regimen of testing blood glucose levels many times a day along with injections of recombinant insulin. Islet transplantation is still not indicated for pediatric patients. Many recent researches have shown that stem cell therapy can be the best choice for treatment this disease. The aims of this research were investigating regeneration of pancreatic β cells of type 1 diabetic mouse after stem cell transplantation. Diabetic mice were induced by streptozocin. Some different kinds of stem cell such as mesenchymal stem cells and nucleated cells derived from human umbilical cord blood; mesenchymal stem cells and hematopoietic stem cells and mononuclear cells derived from murine bone marrow; insulin-secreting cells differentiated from mesenchymal stem cells were used to transplant into diabetic mice. Each diabetic mouse was transplanted with 5×106 cells by one of two ways: inject into pancreas or inject into tail portal vein. Regeneration of β cells was confirmed by decreasing blood glucose level, increasing insulin concentration in blood, body weight and the number of islets of Langerhans in the pancreas. The results showed that transplanting different kinds of stem cells as well as injection methods would give different results for regeneration of β cells. The best result achieved when transplanting insulin producing cells derived from mesenchymal stem cells into diabetic mice by directly injecting into pancreas.

    Keywords diabetic mouse – mesenchymal stem cell – bone marrow – stem cell therapy – type 1 diabetes

    * Author for correspondence: Tel: 84-8-38397719; Fax: 84-8-38967365; E-mail: pvphuc@hcmuns.edu.vn

  • Results of Curing Some Diseases by Stem Cell Transplantation at Stem Cell R&D Laboratory

    Phan Kim Ngoc and Pham Van Phuc. Results of Curing Some Diseases by Stem Cell Transplantation at Stem Cell R&D Laboratory. IFMBE Proceedings, 1, Volume 27, The Third International Conference on the Development of Biomedical Engineering in Vietnam, Part 5, Pages 167-170.

    IFMBE Proceedings, 2010, Volume 27, Part 5, 167-170, DOI: 10.1007/978-3-642-12020-6_41

    Results of Curing Some Diseases by Stem Cell Transplantation at Stem Cell R&D Laboratory

    Phan Kim Ngoc and Pham Van Phuc

    Stem cell therapy in curing dangerous diseases usually is main target of many researches about stem cells. In the world, researching and applying stem cells to cure diseases got some great achievements while there is a few in Viet Nam. In recently years, Laboratory of Stem cell R&D, University of Science, VNU HCM city carried out some researches about preclinical treatment diseases using stem cell therapy. We used some different kinds of stem cells such as mesenchymal stem cells derived from umbilical cord blood to cure bone marrow failure syndrome and bone broken. The results showed that efficiency of cure was different when various methods and kinds of stem cell were applied. These results were bases for developing novel approaches and applying clinical treatment.

    * Author for correspondence: Tel: 84-8-38397719; Fax: 84-8-38967365; E-mail: pvphuc@hcmuns.edu.vn

  • Isolation and characterization of breast cancer stem cells from malignant tumours in Vietnamese…

    Pham Van Phuc, Tran Thi Thanh Khuong, Le Van Dong, Truong Dinh Kiet, Tran Tung Giang and Phan Kim Ngoc (2010). Isolation and characterization of breast cancer stem cells from malignant tumours in Vietnamese women. Journal of Cell and Animal Biology 4(12):163–16.

    Journal of Cell and Animal Biology Vol. 4(12), pp. 163–169, December 2010

    ISSN 1996-0867 ©2010 Academic Journals

    Full Length Research Paper


    Isolation and characterization of breast cancer stem cells from malignant tumours in Vietnamese women


    Pham Van Phuc1*, Tran Thi Thanh Khuong1, Le Van Dong2, Truong Dinh Kiet3, Tran Tung Giang4 and Phan Kim Ngoc1


    1Laboratory of Stem cell Research and Application, University of Science, VNU-HCM, Vietnam.

    2Military Medical University, Ha Noi, Vietnam.

    3University of Medicine – Pharmacy, HCM city, Vietnam.

    4The University of New South Wales, Sydney, Australia.


    *Corresponding author. E-mail: pvphuc@hcmuns.edu.vnphamvanphuc2308@gmail.com. Tel: (84.8)38397719. Fax: (84.8) 38350096.


    Accepted 17 November, 2010


    Abstract

    Cancer stem cells are the origin of tumors and have been isolated successfully from different kinds of tumors. Breast cancer stem cells have been recently identified in breast carcinoma with markers CD44+/CD24-/dim. This population can cause tumor and display stem cell-like properties. However, direct evidences that breast cancer stem cells can be propagated in vitro is still lacking. This research was carried out to isolate and propagate in vitro breast cancer stem cells from tumor biopsy. Breast tumor biopsy was used to isolate breast cancer cells by primary tissue culture. As such, breast cancer stem cells were isolated from breast cancer cells by catcher-tube based cell sorter on flow cytometter machine. These cells were propagated by an in vitro culture in a free serum specific medium. The results showed that the CD44+CD24-/dim cell population that were maintained, were capable of self-renewal and extensive proliferation as clonal non-adherent spherical clusters. Interestingly, cultured cells were CD44+CD24-/dim expressed by the putative stem cell marker Oct-4, resistant with verapamil at 50 µg/ml, and gave rise to new tumors when as few as 1000 cells were injected into the mammary fat pad of immune-deficient mice. This population was a suitable in vitro model to study breast cancer stem cells and develop therapeutic strategies to treat breast cancer.


    Key words: Breast cancer, breast tumor, cancer stem cell, CD44+CD24-/dim

  • Effects of breast cancer stem cell extract primed dendritic cell transplantation on breast cancer…

    Pham Van Phuc, Chi Jee Hou, Nguyen Thi Minh Nguyet, Duong Thanh Thuy, Le Van Dong, Truong Dinh Kiet and Phan Kim Ngoc. Effects of breast cancer stem cell extract primed dendritic cell transplantation on breast cancer tumor murine models. Annual Review & Research in Biology 1(1):1-13, 2011.

    Annual Review & Research in Biology, ISSN: 2231-4776


    Research Paper



    Effects of Breast Cancer Stem Cell Extract Primed Dendritic Cell Transplantation on Breast Cancer Tumor Murine Models


    Pham Van Phuc1*, Chi Jee Hou1, Nguyen Thi Minh Nguyet1, Duong Thanh Thuy1, Le Van Dong2, Truong Dinh Kiet1 and Phan Kim Ngoc1

    1Laboratory of Stem Cell Research and Application, University of Science, Vietnam National University, Ho Chi Minh City, Vietnam;
    2Military Medical University, Ha Noi, Vietnam;

    Abstract

    Cancer stem cells are considered as an origin of cancer. Cancer stem cells can cause tumors in mice models. Recent studies proved the efficacy of some promising therapies to treat cancers. Dendritic cell (DC) therapy is one of the best promising therapies to treat cancer. In recent years, DC therapy is performed by using primed cancer cell antigens of DC to immune organism body. This research aims to combine DC therapy with cancer stem cell antigen for treating breast cancer in murine models. DCs were derived from mouse bone marrow monocytes. Then they were primed with the breast cancer cell antigen prior to employ into the tumor mice model. This was performed to determine whether the DCs would capture and eventually migrate, be present in the spleen and present the cancer antigens to autologous CD8 T cells; induce the activation of the CTL response. The existence of tumors in mice was evaluated after 15-60 days from transplantation. The results showed that 40% mice of the experimental group, with injected breast cancer stem cell antigen loaded DCs, got tumors after 18 transplantation days. But in control group 100% mice got tumors after 15 transplantation days. It is also noticed that transplanted DCs could migrate into spleen, stimulate CD8 T cells and CD45 T cells proliferation. Specially, the ratio of CD8 T cells strongly increased in comparison to control or normal mice. These results are important and provides most required initial platform to do further experiment. Results of this study also established a promising novel targeting therapy for cancer, especially for breast cancer.

     

    Keywords : Breast cancer stem cell, cancer stem cell, dendritic cell, dendritic cell therapy, immunotherapy;

    * Author for correspondence: Tel: 84-8-38397719; Fax: 84-8-38967365; E-mail: pvphuc@hcmuns.edu.vn

  • Stem Cell Therapy for Islet Regeneration

    Stem Cells in Clinic and Research

    Book edited by Ali Gholamrezanezhad

    ISBN 978-953-307-797-0, Hard cover, 804 pages

    Published: August 23, 2011 under CC BY-NC-SA 3.0 license.

    Chapter 22: Stem Cell Therapy for Islet Regeneration

     By Phuc Pham Van
    DOI: 10.5772/17588

    Based on our current understanding of cell biology and strong supporting evidence from previous experiences, different types of human stem cell populations are capable of undergoing differentiation or trans-differentiation into functionally and biologically active cells for use in therapeutic purposes. So far, progress regarding the use of both in vitro and in vivo regenerative medicine models already offers hope for the application of different types of stem cells as a powerful new therapeutic option to treat different diseases that were previously considered to be untreatable. Remarkable achievements in cell biology resulting in the isolation and characterization of various stem cells and progenitor cells has increased the expectation for the development of a new approach to the treatment of genetic and developmental human diseases. Due to the fact that currently stem cells and umbilical cord banks are so strictly defined and available, it seems that this mission is investigationally more practical than in the past. On the other hand, studies performed on stem cells, targeting their conversion into functionally mature tissue, are not necessarily seeking to result in the clinical application of the differentiated cells; In fact, still one of the important goals of these studies is to get acquainted with the natural process of development of mature cells from their immature progenitors during the embryonic period onwards, which can produce valuable results as knowledge of the developmental processes during embryogenesis. For example, the cellular and molecular mechanisms leading to mature and adult cells developmental abnormalities are relatively unknown. This lack of understanding stems from the lack of a good model system to study cell development and differentiation. Hence, the knowledge reached through these studies can prove to be a breakthrough in preventing developmental disorders. Meanwhile, many researchers conduct these studies to understand the molecular and cellular basis of cancer development. The fact that cancer is one of the leading causes of death throughout the world, highlights the importance of these researches in the fields of biology and medicine.

    Introduction

    Diabetes mellitus is an endocrine disorder characterised by inadequate production or use of insulin, resulting in abnormally high blood glucose levels. High blood glucose leads to the formation of reactive advanced glycation end-products (Feldman et al., 1997), which are responsible for complications such as blindness, kidney failure, cardiovascular disease, stroke, neuropathy and vascular dysfunction. Diabetes mellitus is classified as either type 1 or type 2. Type 1 diabetes mellitus (insulin-dependent diabetes mellitus) results from the autoimmune destruction of the pancreatic beta cells, whereas type 2 diabetes mellitus (non-insulin-dependent diabetes mellitus) results from insulin resistance and impaired glucose tolerance.

    Approximately 7.8% (23.6 million people) of the US population has been diagnosed with diabetes mellitus, and another 57 million people are likely to develop diabetes mellitus in the coming years (American Diabetes Association, 2007). The number of people with diabetes mellitus is set to continue to rapidly increase between now and 2030, especially in developing countries.

    Over the last decade, a new form of treatment called islet transplantation therapy was thought to provide good patient outcomes; however, few islets are available for transplantation. Typically, the pooled islets isolated from two pancreases are enough to treat a single patient. Since the enormous potential of stem cells was discovered, it was hoped that they would provide the most effective treatment for diabetes mellitus. Over the past two decades, hundreds of studies have looked at the potential of stem cell therapy for treating diabetes mellitus. Successful stem cell therapy would eliminate the cause of the disease and lead to stable, long-term results; hence, the term “pancreatic regeneration” was coined. The hypothesis was that stem cells could regenerate the damaged pancreas. After careful consideration of the aetiology of diabetes mellitus, scientists have put forward two general treatment strategies: stem cell therapy to treat the autoimmune aspect of the disease, and stem cell therapy to treat the degenerative aspect of the disease. In this review, we focus on stem cell-based therapies aimed at islet regeneration through stem cell or insulin-producing cell (IPC) transplantation. We will also discuss the latest strategies for treating both type 1 and type 2 diabetes mellitus using stem cell therapy, along with the (initially promising) results.