1.Adult stem cells and possible mechanisms of its differentiation--editorial.
Zhuo-Yan ZHOU ; Mo YANG ; Yue-Hua JIANG
Journal of Experimental Hematology 2005;13(3):353-357
Adult stem cells are the multi-potential cells, which exist in fetal and adult tissues. It can reproduce itself (undergo self-renewal) or give rise to more specialized (differentiated) cells. Under certain inducing conditions, adult stem cells can acquire the ability to differentiate into different tissue cells. Multipotent adult progenitor cells (MAPC), an alternative name of adult stem cell given by Catherine Verfaillie, existing in bone marrow, can differentiate into cells with characteristics of mesodermal, neuroectodermal, and endodermal lineages in vitro at the single-cell level. MAPC can also contribute to most cell types when injected into the blastocyst. Adult stem cell differentiation implies that different cell lineages are derived from a single initial cell; all differentiated cell types are functional in vitro and in vivo; and engraftment is robust and persistent in the physiological and pathological situations. The possible mechanisms may underlie the differentiation: various tissue-specific stem cells are present in different organs; adult stem cells would be reprogrammed when removed from their usual microenvironment and introduced into a different niche that imparts signals to activate a novel genetic program needed for the new cell fate. And true multi-potential stem cells persist in postnatal life. In the future, multi-potent adult stem cells might then be used for therapies of degenerative or genetic disorders of multiple different organs.
Adult Stem Cells
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cytology
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Cell Differentiation
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Humans
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Multipotent Stem Cells
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cytology
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Stem Cell Transplantation
2.MHC Antigen Expressions in Human Embryonic Neural Stem Cells and Adult Breast Epithelial Stem Cells.
Eun Mi LEE ; Jae Young KIM ; Donghee KIM ; Bum Rae CHO ; Hyun Sook KOH ; Jae Seok YANG ; Jung Sang LEE ; Curie AHN
The Journal of the Korean Society for Transplantation 2003;17(2):105-112
PURPOSE: Due to their unique capacity to self-renew and for multiple differentiation, stem cells are considered potent candidates for cell replacement therapy in many devastating diseases. However, studies on immune rejection, which is a major problem facing successful stem cell therapy, are rare. Thus, we examined MHC expression of human stem cells and effects of IFN-gamma on the MHC class I expression of the cells in order to determine whether human stem cells might be rejected after transplantation. METHODS: The MHC antigen expressions of human embryonic neural stem cell line (HB1.F3) and human breast epithelial stem cell line (M13SV1) were examined by RT-PCR and FACS. The effects of varying concentrations of IFN-gamma and of varying incubation times with IFN-gamma on the expression of MHC class I antigens in these stem cell lines were also examined by FACS. RESULTS: The results show low expression levels of MHC class I antigens on surfaces of these cells. A dramatic induction of MHC class I expression was observed when the cells were treated with IFN-gamma. Maximal induction of MHC class I antigen expression in HB1.F3 and M13SV1 cells was observed at above the concentrations of 20 ng/mL and 5 ng/mL of IFN-gamma 48 h after treatment, respectively. Elevated MHC class I levels in HB1.F3 and M13SV1 cells were sustained for 48 h and 72 h after withdrawing IFN-gamma, respectively. CONCLUSION: These results suggest that human stem cells express high levels of MHC class I antigens, and thus may be rejected on transplantation unless they are modified. Therefore, in addition to studies on stem cell differentiation, studies on overcoming the immunological barriers to stem cell transplantation are prerequisite for successful clinical application of stem cell therapy.
Adult*
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Breast*
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Histocompatibility Antigens Class I
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Humans*
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Neural Stem Cells*
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Stem Cell Transplantation
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Stem Cells*
3.Stem Cell Properties of Therapeutic Potential.
The Korean Journal of Gastroenterology 2011;58(3):125-132
Stem cell research is a innovative technology that focuses on using undifferentiated cells able to self-renew through the asymmetrical or symmetrical divisions. Three types of stem cells have been studied in laboratory including embryonic stem cell, adult stem cells and induced pluripotent stem cells. Embryonic stem cells are pluripotent stem cells derived from the inner cell mass and it can give rise to any fetal or adult cell type. Adult stem cells are multipotent, have the ability to differentiate into a limited number of specialized cell types, and have been obtained from the bone marrow, umbilical cord blood, placenta and adipose tissue. Stem cell therapy is the most promising therapy for several degenerative and devastating diseases including digestive tract disease such as liver failure, inflammatory bowel disease, Celiac sprue, and pancreatitis. Further understanding of biological properties of stem cells will lead to safe and successful stem cell therapies.
Adult Stem Cells/cytology/metabolism/transplantation
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Embryonic Stem Cells/cytology/metabolism/transplantation
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Humans
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Induced Pluripotent Stem Cells/cytology/metabolism/transplantation
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Stem Cells/*cytology/metabolism
4.Successful Chemotherapy Following Autologous Stem Cell Transplantation in Multiple Myeloma and Multi-organ Dysfunction with Infiltration of Eosinophils: A Case Report.
Ho Sup LEE ; Lee Chun PARK ; Seong Hoon SHIN ; Sang Uk LEE ; Hee Kyung CHANG ; Bang HUH ; Gyoo Sik JUNG ; Mi Hyang KIM ; Yang Soo KIM
Cancer Research and Treatment 2011;43(3):199-203
Eosinophils are derived from hematopoietic stem cells. Peripheral blood eosinophilia is defined as an absolute eosinophil count of > or =0.5x10(9)/L. Eosinophilia is classified into primary or clonal eosinophilia, secondary eosinophilia, and idiopathic categories including idiopathic hypereosinophilic syndrome. Both hematopoietic and solid neoplasms may be associated with peripheral blood eosinophilia, but multiple myeloma is rarely associated with eosinophilia. We now report the case of a 31-year-old man with multiple myeloma associated with marked eosinophilia who developed multiple organ dysfunction with infiltration of eosinophils. He recovered after treatment with chemotherapy followed by autologous stem cell transplantation.
Adult
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Eosinophilia
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Eosinophils
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Hematopoietic Stem Cells
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Humans
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Hypereosinophilic Syndrome
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Multiple Myeloma
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Stem Cell Transplantation
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Stem Cells
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Transplantation, Autologous
5.Successful Chemotherapy Following Autologous Stem Cell Transplantation in Multiple Myeloma and Multi-organ Dysfunction with Infiltration of Eosinophils: A Case Report.
Ho Sup LEE ; Lee Chun PARK ; Seong Hoon SHIN ; Sang Uk LEE ; Hee Kyung CHANG ; Bang HUH ; Gyoo Sik JUNG ; Mi Hyang KIM ; Yang Soo KIM
Cancer Research and Treatment 2011;43(3):199-203
Eosinophils are derived from hematopoietic stem cells. Peripheral blood eosinophilia is defined as an absolute eosinophil count of > or =0.5x10(9)/L. Eosinophilia is classified into primary or clonal eosinophilia, secondary eosinophilia, and idiopathic categories including idiopathic hypereosinophilic syndrome. Both hematopoietic and solid neoplasms may be associated with peripheral blood eosinophilia, but multiple myeloma is rarely associated with eosinophilia. We now report the case of a 31-year-old man with multiple myeloma associated with marked eosinophilia who developed multiple organ dysfunction with infiltration of eosinophils. He recovered after treatment with chemotherapy followed by autologous stem cell transplantation.
Adult
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Eosinophilia
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Eosinophils
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Hematopoietic Stem Cells
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Humans
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Hypereosinophilic Syndrome
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Multiple Myeloma
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Stem Cell Transplantation
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Stem Cells
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Transplantation, Autologous
6.Stem cell therapy in pain medicine
Yong Hee HAN ; Kyung Hoon KIM ; Salahadin ABDI ; Tae Kyun KIM
The Korean Journal of Pain 2019;32(4):245-255
Stem cells are attracting attention as a key element in future medicine, satisfying the desire to live a healthier life with the possibility that they can regenerate tissue damaged or degenerated by disease or aging. Stem cells are defined as undifferentiated cells that have the ability to replicate and differentiate themselves into various tissues cells. Stem cells, commonly encountered in clinical or preclinical stages, are largely classified into embryonic, adult, and induced pluripotent stem cells. Recently, stem cell transplantation has been frequently applied to the treatment of pain as an alternative or promising approach for the treatment of severe osteoarthritis, neuropathic pain, and intractable musculoskeletal pain which do not respond to conventional medicine. The main idea of applying stem cells to neuropathic pain is based on the ability of stem cells to release neurotrophic factors, along with providing a cellular source for replacing the injured neural cells, making them ideal candidates for modulating and possibly reversing intractable neuropathic pain. Even though various differentiation capacities of stem cells are reported, there is not enough knowledge and technique to control the differentiation into desired tissues in vivo. Even though the use of stem cells is still in the very early stages of clinical use and raises complicated ethical problems, the future of stem cells therapies is very bright with the help of accumulating evidence and technology.
Adult
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Adult Stem Cells
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Aging
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Cell Differentiation
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Embryonic Stem Cells
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Humans
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Induced Pluripotent Stem Cells
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Musculoskeletal Pain
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Nerve Growth Factors
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Neuralgia
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Osteoarthritis
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Stem Cell Transplantation
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Stem Cells
7.Regulation of the self-renewal and differentiation of spermatogonial stem cells.
National Journal of Andrology 2013;19(11):963-967
Spermatogonial stem cells (SSCs) play an important role in spermatogenesis and have a unique mode of replication. A single SSC can produce two differentiating cells, or one stem cell and one differentiating cell. The self-renewal and differentiation of SSCs are precisely regulated as relating the niche of SSCs, glial cell line-derived neurotrophic factor, and several signaling pathways. This article reviews the self-renewal and differentiation of SSCs and their regulation mechanisms, which may offer a deeper insight into spermatogenesis and male infertility and pave a theoretical ground for studying testicular tumorigenesis and searching for new potential approaches to the treatment of testicular cancer and other related diseases.
Adult Stem Cells
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cytology
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Cell Differentiation
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Cells, Cultured
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Humans
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Male
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Spermatogenesis
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Spermatogonia
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cytology
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Stem Cell Transplantation
8.Neural Stem Cells for Neurological Disorders.
Jae Kyu ROH ; Manho KIM ; Kon CHU
Journal of the Korean Medical Association 2004;47(10):940-947
Recent progress shows that neurons suitable for transplantation can be generated from neural stem cells (NSCs) in culture, and that the adult brain produces new neurons from its own stem cells in response to injury. In this article, we discuss how the subventricular zone of the forebrain is the most active neurogenetic area and the richest source of NSCs. This review also focuses on the nature and functional properties of NSCs of the adult mammalian brain, and we propose our views on the strategy from bench to the clinic with particular concerns and considerations.
Adult
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Brain
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Humans
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Nervous System Diseases*
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Neural Stem Cells*
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Neurons
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Prosencephalon
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Stem Cells
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Transplantation
9.Factors Influencing Health Related Quality of Life in Adult Survivors of Haematopoietic Stem Cell Transplantation.
Asian Oncology Nursing 2017;17(4):220-228
PURPOSE: The aim of the study is to evaluate the health-related quality of life, psychological symptoms, distress, and sense of coherence in adult haematopoietic stem cell transplantation survivors. METHODS: Fifty two survivors completed four questionnaires after the transplantation. The questionnaires were the Functional Assessment of Cancer Therapy-BMT Scale, the National Cancer Center Psychological Symptom Inventory, the Distress Thermometer, and the Sense of Coherence scale. RESULTS: Quality of life was positively correlated with sense of coherence, whereas sense of coherence was negatively correlated with all psychological symptoms and distress. Hierarchical regression analyses revealed that sense of coherence was the only significant predictor of quality of life after controlling for sex and age at transplantation. Model 2 explained 33.2% of the total variance of quality of life. CONCLUSION: Supporting patients towards improving comprehensibility, manageability and meaningfulness, the three components of sense of coherence, may be beneficial and improve outcomes. Individually pre-transplant and post-transplant assessments of sense of coherence may be of clinical importance, in order to identify patients with unmet needs and to provide rolonged support.
Adult*
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Hematopoietic Stem Cell Transplantation
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Humans
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Quality of Life*
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Sense of Coherence
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Stem Cell Transplantation*
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Stem Cells*
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Survivors*
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Symptom Assessment
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Thermometers
10.New techniques for umbilical cord blood transplantation.
Journal of Southern Medical University 2013;33(12):1839-1843
Umbilical cord blood is an alternative hematopoietic stem cell source for treatment of hematological diseases that can be cured by allogeneic hematopoietic stem cell transplantation. Since the first case of umbilical cord blood transplantation performed successfully in a child with Fanconi anemia, the field of umbilical cord blood transplantation has grown exponentially, and a great progress has been made worldwide in the treatment of children with malignant hematological diseases, including some congenital metabolic disorders. Umbilical cord blood transplantation was initially intended only in the treatment of pediatric patients, given the small volume collected and the low hematopoietic stem cell dose infused. In recent years, the application of new techniques for hematopoietic stem cell transplantation has greatly improved the outcomes of umbilical cord blood transplantation in adult patients. In this review article, we summarize the latest techniques for umbilical cord blood transplantation.
Adult
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Child
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Cord Blood Stem Cell Transplantation
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Fetal Blood
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Hematopoietic Stem Cell Transplantation
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Hematopoietic Stem Cells
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Humans