1.Hematopoietic Differentiation of Embryoid Bodies Derived from the Human Embryonic Stem Cell Line SNUhES3 in Co-culture with Human Bone Marrow Stromal Cells.
Seok Jin KIM ; Byung Soo KIM ; Suck Won RYU ; Ji Hyun YOO ; Jee Hyun OH ; Chang Hee SONG ; Sun Haeng KIM ; Dong Seop CHOI ; Jae Hong SEO ; Chul Won CHOI ; Sang Won SHIN ; Yeul Hong KIM ; Jun Suk KIM
Yonsei Medical Journal 2005;46(5):693-699
Human embryonic stem (ES) cells can be induced to differentiate into hematopoietic precursor cells via two methods: the formation of embryoid bodies (EBs) and co-culture with mouse bone marrow (BM) stromal cells. In this study, the above two methods have been combined by co-culture of human ES-cell-derived EBs with human BM stromal cells. The efficacy of this method was compared with that using EB formation alone. The undifferentiated human ES cell line SNUhES3 was allowed to form EBs for two days, then EBs were induced to differentiate in the presence of a different serum concentration (EB and EB/high FBS group), or co- cultured with human BM stromal cells (EB/BM co-culture group). Flow cytometry and hematopoietic colony-forming assays were used to assess hematopoietic differentiation in the three groups. While no significant increase of CD34+/CD45- or CD34+/CD38- cells was noted in the three groups on days 3 and 5, the percentage of CD34+/CD45- cells and CD34+/ CD38- cells was significantly higher in the EB/BM co-culture group than in the EB and EB/high FBS groups on day 10. The number of colony-forming cells (CFCs) was increased in the EB/BM co-culture group on days 7 and 10, implying a possible role for human BM stromal cells in supporting hematopoietic differentiation from human ES cell-derived EBs. These results demonstrate that co-culture of human ES-cell-derived EBs with human BM stromal cells might lead to more efficient hematopoietic differentiation from human ES cells cultured alone. Further study is warranted to evaluate the underlying mechanism.
Stromal Cells/physiology
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Stem Cells/*cytology
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Humans
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Hematopoietic Stem Cells/*cytology
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Embryo/*cytology
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Coculture Techniques
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Cells, Cultured
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*Cell Differentiation
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Bone Marrow Cells/*cytology
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Antigens, CD45/analysis
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Antigens, CD38/analysis
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Antigens, CD34/analysis
2.A Case of Non-secretory Myeloma with Crystal-storing Histiocytosis.
Soon Ho PARK ; Jeong Yeal AHN ; Yiel Hea SEO ; Pil Hwan PARK ; Kyung Hee KIM ; Young Hee SONG ; Ji Hun JEONG ; Jae Hoon LEE
The Korean Journal of Laboratory Medicine 2010;30(6):580-584
Crystal-storing histiocytosis (CSH) is a rare event observed in association with lymphoproliferative diseases, and mainly occurrs in plasma cell dyscrasias. It is presumed to be an intra-lysosomal accumulation of the secreted paraproteins. Crystal formation can be seen inside histiocyte-like cells with phagocytosed crystalline inclusions in the bone marrow and extramedullary sites. CSH is a rare morphological entity with poor prognostic implications and may be confused with Gaucher or pseudo-Gaucher cells. Herein we report a case of non-secretory myeloma associated with CSH showing a poor clinical course. A 79-yr-old male presenting with dizziness was evaluated in hematology department for anemia. Laboratory tests revealed Hb of 4.9 g/dL and beta2-microglobulin of 21,000 ng/mL (reference range, 0-370). Presence of monoclonal protein was not detected on protein electrophoresis and immunofixation in serum and urine. However, serum free light chain assay showed an increased kappa-light chain level of 126 mg/L (reference range, 3.3-19.4) resulting in an increased kappa/lambda ratio. The bone marrow touch print showed numerous plasma cells and crystal-laden histiocytes and immunohistochemical stainings on bone marrow biopsy revealed positivity for CD38, CD56 and kappa in the plasma cells and CD68 and kappa in crystal-laden histiocytes.
Aged
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Antigens, CD/metabolism
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Antigens, CD38/metabolism
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Antigens, Differentiation, Myelomonocytic/metabolism
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Bone Marrow Cells/pathology
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Histiocytosis/complications/*diagnosis/radiography
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Humans
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Immunoglobulin kappa-Chains/analysis
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Male
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Multiple Myeloma/complications/*diagnosis/radiography
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Tomography, X-Ray Computed
3.Extramedullary relapse of multiple myeloma presenting as massive upper gastrointestinal bleeding: a rare complication.
Bulent YASAR ; Pembegul GUNES ; Ozgur GULER ; Selma YAGCI ; Dilek BENEK
The Korean Journal of Internal Medicine 2015;30(4):538-539
No abstract available.
Aged
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Antigens, CD38/analysis
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Biomarkers, Tumor/analysis
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Biopsy
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Gastrointestinal Hemorrhage/diagnosis/*etiology/therapy
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Gastroscopy
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Hematemesis/etiology
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Humans
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Immunohistochemistry
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Male
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Melena/etiology
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Membrane Glycoproteins/analysis
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Multiple Myeloma/*complications/immunology/pathology/therapy
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Recurrence
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Stomach Neoplasms/*complications/immunology/pathology/therapy