stem cell-based drug discovery and drug rescue Search Results


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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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BioMimetic Therapeutics mesenchymal stem cell-based drug delivery strategy
Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Progenitor Cell Therapy Inc ipsc-derived dopamine progenitor cell therapy
Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Figure 1. Nuclear pattern <t>of</t> <t>Cajal</t> bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 <t>mESCs</t> and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.
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Image Search Results


Figure 1. Nuclear pattern of Cajal bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 mESCs and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.

Journal: Nucleus (Austin, Tex.)

Article Title: Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies.

doi: 10.4161/nucl.29229

Figure Lengend Snippet: Figure 1. Nuclear pattern of Cajal bodies in several cell types. (A) Cajal body (green) morphology was studied in mouse embryonic fibroblasts (MEFs), multiple myeloma cells (OPM2 and MOLP8), K562 leukemia cells, and U2OS human osteosarcoma cells. (B) Nuclear distribution of coilin in embryonic stem cells. Coilin was homogeneously distributed in interphase nuclei of human ESCs, or accumulated into body-like structures (Cajal bodies) in hESCs. (C) Cajal bodies were observed in pluripotent mouse ESCs (line D3), and in GOWT1 mESCs and in their differentiated counterparts. (D) Morphological association between Cajal bodies (green) and γ-H2AX-positive foci (red) in non-irradiated and γ-irradiated U2OS cells.

Article Snippet: We analyzed the nuclear pattern of Cajal bodies in mouse embryonic stem cells (mESCs) (line D3, ATCC), in GOWT1 cells (gift from Dr Hitoshi Niwa), and in human ESCs (hESCs).31 Differentiation of mouse ESCs was induced by alltrans retinoic acid according to previously published protocols.32 We also used HeLa cells stably expressing GFP-colin (a generous gift from the laboratory of Prof Angus Lamond, University of Dundee16).

Techniques: Irradiation

Figure 5. Recruitment of coilin to UVA-induced DNA lesions. (A) In live U2OS cells transiently expressing GFP-coilin and HeLa cells stably expressing GFP-coilin. Coilin was recruited to micro-irradiated genomic regions. This was also observed in transiently transfected D3 mESCs. These experiments were performed with BrdU pre-sensitization. (B) Recruitment of coilin to UVA-induced DNA lesions in HeLa cells stably expressing GFP-coilin, but lacking CBs. (C) Cells were locally irradiated using a UVA-laser in defined regions of interest (ROI) and endogenous coilin was analyzed under conditions of (a) BrdU pre-sensitization or (b) without BrdU pre-sensitization. (c) CPDs were analyzed without BrdU pre-sensitization. CPDs were visualized by red fluorescence and CBs as green. Experiments were performed in HeLa cells stably expressing GFP-coilin (green). The cell nuclei were clearly visible before local micro- irradiation, and GFP fluorescence was maintained after formaldehyde fixation and immunostaining. To assess endogenous coilin levels, HeLa cells were micro-irradiated and endogenous coilin and CPDs were visual- ized using antibodies (panel Cc).

Journal: Nucleus (Austin, Tex.)

Article Title: Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies.

doi: 10.4161/nucl.29229

Figure Lengend Snippet: Figure 5. Recruitment of coilin to UVA-induced DNA lesions. (A) In live U2OS cells transiently expressing GFP-coilin and HeLa cells stably expressing GFP-coilin. Coilin was recruited to micro-irradiated genomic regions. This was also observed in transiently transfected D3 mESCs. These experiments were performed with BrdU pre-sensitization. (B) Recruitment of coilin to UVA-induced DNA lesions in HeLa cells stably expressing GFP-coilin, but lacking CBs. (C) Cells were locally irradiated using a UVA-laser in defined regions of interest (ROI) and endogenous coilin was analyzed under conditions of (a) BrdU pre-sensitization or (b) without BrdU pre-sensitization. (c) CPDs were analyzed without BrdU pre-sensitization. CPDs were visualized by red fluorescence and CBs as green. Experiments were performed in HeLa cells stably expressing GFP-coilin (green). The cell nuclei were clearly visible before local micro- irradiation, and GFP fluorescence was maintained after formaldehyde fixation and immunostaining. To assess endogenous coilin levels, HeLa cells were micro-irradiated and endogenous coilin and CPDs were visual- ized using antibodies (panel Cc).

Article Snippet: We analyzed the nuclear pattern of Cajal bodies in mouse embryonic stem cells (mESCs) (line D3, ATCC), in GOWT1 cells (gift from Dr Hitoshi Niwa), and in human ESCs (hESCs).31 Differentiation of mouse ESCs was induced by alltrans retinoic acid according to previously published protocols.32 We also used HeLa cells stably expressing GFP-colin (a generous gift from the laboratory of Prof Angus Lamond, University of Dundee16).

Techniques: Expressing, Stable Transfection, Irradiation, Transfection, Fluorescence, Immunostaining

Figure 9. Localized movement of Cajal bodies. (A) Average enclosing ellipses (yellow) calculated for Cajal bodies in HeLa cells, D3 mESCs, and U2OS cells. Non-treated cells were used as control cell population, and data were compared with average enclosing ellipse of Cajal bodies in cells irradiated by 5 Gy of γ-rays. Tracking of ellipse centroids is shown in blue. Selected ellipses are enlarged in individual frames. Small red dots represent the starting points of tracking analysis. (B) Data represent average enclosing ellipse areas in non-irradiated and γ-irradiated HeLa cells, D3 mESCs, and U2OS cells. (C) Average enclosing ellipse area per Cajal body area in HeLa cells, D3 mESCs, and U2OS cells. Data in panels B and C represent mean ± standard error (S.E.). Asterisks in panels (B) and (C) show statistically significant differences from control values at P ≤ 0.05. Analysis was performed by Student’s t test.

Journal: Nucleus (Austin, Tex.)

Article Title: Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies.

doi: 10.4161/nucl.29229

Figure Lengend Snippet: Figure 9. Localized movement of Cajal bodies. (A) Average enclosing ellipses (yellow) calculated for Cajal bodies in HeLa cells, D3 mESCs, and U2OS cells. Non-treated cells were used as control cell population, and data were compared with average enclosing ellipse of Cajal bodies in cells irradiated by 5 Gy of γ-rays. Tracking of ellipse centroids is shown in blue. Selected ellipses are enlarged in individual frames. Small red dots represent the starting points of tracking analysis. (B) Data represent average enclosing ellipse areas in non-irradiated and γ-irradiated HeLa cells, D3 mESCs, and U2OS cells. (C) Average enclosing ellipse area per Cajal body area in HeLa cells, D3 mESCs, and U2OS cells. Data in panels B and C represent mean ± standard error (S.E.). Asterisks in panels (B) and (C) show statistically significant differences from control values at P ≤ 0.05. Analysis was performed by Student’s t test.

Article Snippet: We analyzed the nuclear pattern of Cajal bodies in mouse embryonic stem cells (mESCs) (line D3, ATCC), in GOWT1 cells (gift from Dr Hitoshi Niwa), and in human ESCs (hESCs).31 Differentiation of mouse ESCs was induced by alltrans retinoic acid according to previously published protocols.32 We also used HeLa cells stably expressing GFP-colin (a generous gift from the laboratory of Prof Angus Lamond, University of Dundee16).

Techniques: Control, Irradiation

Figure 8. FRAP analysis of coilin diffusion in various nuclear regions. Kinetics of GFP-coilin were studied in nucleoli, DNA lesions, nucleoplasm, and non-irradiated Cajal bodies in (A) D3 mESCs; (B) U2OS cells; and (C) HeLa cells. FRAP data were normalized to 1, and data represent means ± standard error (S.E.).

Journal: Nucleus (Austin, Tex.)

Article Title: Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies.

doi: 10.4161/nucl.29229

Figure Lengend Snippet: Figure 8. FRAP analysis of coilin diffusion in various nuclear regions. Kinetics of GFP-coilin were studied in nucleoli, DNA lesions, nucleoplasm, and non-irradiated Cajal bodies in (A) D3 mESCs; (B) U2OS cells; and (C) HeLa cells. FRAP data were normalized to 1, and data represent means ± standard error (S.E.).

Article Snippet: We analyzed the nuclear pattern of Cajal bodies in mouse embryonic stem cells (mESCs) (line D3, ATCC), in GOWT1 cells (gift from Dr Hitoshi Niwa), and in human ESCs (hESCs).31 Differentiation of mouse ESCs was induced by alltrans retinoic acid according to previously published protocols.32 We also used HeLa cells stably expressing GFP-colin (a generous gift from the laboratory of Prof Angus Lamond, University of Dundee16).

Techniques: Diffusion-based Assay, Irradiation