LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 25

Search options

  1. Article ; Online: An Alternative Cell Therapy for Cancers

    Li-Jie Hsu / Chao-Lin Liu / Ming-Ling Kuo / Chia-Ning Shen / Chia-Rui Shen

    Biomedicines, Vol 9, Iss 1323, p

    Induced Pluripotent Stem Cell (iPSC)-Derived Natural Killer Cells

    2021  Volume 1323

    Abstract: Cell therapy is usually defined as the treatment or prevention of human disease by supplementation with cells that have been selected, manipulated, and pharmacologically treated or altered outside the body (ex vivo). Induced pluripotent stem cells (iPSCs) ...

    Abstract Cell therapy is usually defined as the treatment or prevention of human disease by supplementation with cells that have been selected, manipulated, and pharmacologically treated or altered outside the body (ex vivo). Induced pluripotent stem cells (iPSCs), with their unique characteristics of indefinite expansion in cultures and genetic modifications, represent an ideal cell source for differentiation into specialized cell types. Cell therapy has recently become one of the most promising therapeutic approaches for cancers, and different immune cell types are selected as therapeutic platforms. Natural killer (NK) cells are shown to be effective tumor cell killers and do not cause graft-vs-host disease (GVHD), making them excellent candidates for, and facilitating the development of, “off-the-shelf” cell therapies. In this review, we summarize the progress in the past decade in the advent of iPSC technology and review recent developments in gene-modified iPSC-NK cells as readily available “off-the-shelf” cellular therapies.
    Keywords induced pluripotent stem cells (iPSCs) ; natural killer cells (NK cells) ; cell therapy ; Biology (General) ; QH301-705.5
    Subject code 610
    Language English
    Publishing date 2021-09-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  2. Article ; Online: Transparent tissue in solid state for solvent-free and antifade 3D imaging

    Fu-Ting Hsiao / Hung-Jen Chien / Ya-Hsien Chou / Shih-Jung Peng / Mei-Hsin Chung / Tzu-Hui Huang / Li-Wen Lo / Chia-Ning Shen / Hsiu-Pi Chang / Chih-Yuan Lee / Chien-Chia Chen / Yung-Ming Jeng / Yu-Wen Tien / Shiue-Cheng Tang

    Nature Communications, Vol 14, Iss 1, Pp 1-

    2023  Volume 12

    Abstract: Abstract Optical clearing with high-refractive-index (high-n) reagents is essential for 3D tissue imaging. However, the current liquid-based clearing condition and dye environment suffer from solvent evaporation and photobleaching, causing difficulties ... ...

    Abstract Abstract Optical clearing with high-refractive-index (high-n) reagents is essential for 3D tissue imaging. However, the current liquid-based clearing condition and dye environment suffer from solvent evaporation and photobleaching, causing difficulties in maintaining the tissue optical and fluorescent features. Here, using the Gladstone-Dale equation [(n−1)/density=constant] as a design concept, we develop a solid (solvent-free) high-n acrylamide-based copolymer to embed mouse and human tissues for clearing and imaging. In the solid state, the fluorescent dye-labeled tissue matrices are filled and packed with the high-n copolymer, minimizing scattering in in-depth imaging and dye fading. This transparent, liquid-free condition provides a friendly tissue and cellular environment to facilitate high/super-resolution 3D imaging, preservation, transfer, and sharing among laboratories to investigate the morphologies of interest in experimental and clinical conditions.
    Keywords Science ; Q
    Language English
    Publishing date 2023-06-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article ; Online: Generation of three induced pluripotent stem cell lines from type 2 diabetic patients with ocular complications

    Edward Po-Fan Chu / Candy Hsin-Hua Cho / Wen-Jane Lee / I-Te Lee / I-Fen Cheng / Tzu-Chien Kuo / Ruei-Ying Chen / Wayne Huey-Herng Sheu / Chia-Ning Shen

    Stem Cell Research, Vol 49, Iss , Pp 102109- (2020)

    2020  

    Abstract: Retinopathy is a well-known ocular complication that occurs in patients with type 2 diabetes (T2D). Recent evidence also indicates that diabetic patients have an increased prevalence of dry eye syndrome. However, the etiologies of both diabetic ... ...

    Abstract Retinopathy is a well-known ocular complication that occurs in patients with type 2 diabetes (T2D). Recent evidence also indicates that diabetic patients have an increased prevalence of dry eye syndrome. However, the etiologies of both diabetic retinopathy (DR) and dry eye disease are complex, and their associations with T2D remains to be fully understood. Patient-derived human induced pluripotent stem cells (hiPSCs) enable the generation of disease-specific retinal tissues such as retinal pigment epithelium and lacrimal gland to model disease pathogenesis. Here, we describe the establishment of three hiPSC lines from T2D patients with PDR or dry eye disease.
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article ; Online: Correction

    Amani Al-Adsani / Zoë D Burke / Daniel Eberhard / Katherine L Lawrence / Chia-Ning Shen / Anil K Rustgi / Hiroshi Sakaue / J Mark Farrant / David Tosh

    PLoS ONE, Vol 14, Iss 7, p e

    Dexamethasone Treatment Induces the Reprogramming of Pancreatic Acinar Cells to Hepatocytes and Ductal Cells.

    2019  Volume 0219419

    Abstract: This corrects the article DOI:10.1371/journal.pone.0013650.]. ...

    Abstract [This corrects the article DOI:10.1371/journal.pone.0013650.].
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  5. Article ; Online: Establishment of three human induced pluripotent stem cell lines from a type 1 diabetic family harboring sequence variants associated with autoimmunity

    Edward Po-Fan Chu / Chia-Hung Lin / Candy Hsin-Hua Cho / I-Fen Cheng / Tzu-Chien Kuo / Ruei-Ying Chen / Chia-Nan Liao / Jen-Chien Cheng / Jason Isheng Tsai / Po-Chuan Wang / Shing-Jyh Chang / Chia-Ning Shen

    Stem Cell Research, Vol 49, Iss , Pp 102029- (2020)

    2020  

    Abstract: Type 1 diabetes (T1D) is characterized by the autoimmune destruction of insulin-producing β cells. Genetic studies have identified > 60 T1D risk loci that harbor genes with disease-causative alleles. However, determining the biological effects of such ... ...

    Abstract Type 1 diabetes (T1D) is characterized by the autoimmune destruction of insulin-producing β cells. Genetic studies have identified > 60 T1D risk loci that harbor genes with disease-causative alleles. However, determining the biological effects of such loci is often difficult due to limited tissue availability. Disease-specific human induced pluripotent stem cells (hiPSCs) are a valuable resource for modeling T1D pathogenesis. In particular, families with complete disease penetrance offer an opportunity to further dissect T1D risk loci. Here, we describe the generation of three hiPSC lines from a T1D family with sequence variants associated with autoimmunity.
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  6. Article ; Online: Lumenal Galectin-9-Lamp2 interaction regulates lysosome and autophagy to prevent pathogenesis in the intestine and pancreas

    Janaki N. Sudhakar / Hsueh-Han Lu / Hung-Yu Chiang / Ching-Shu Suen / Ming-Jing Hwang / Sung-Yu Wu / Chia-Ning Shen / Yao-Ming Chang / Fu-An Li / Fu-Tong Liu / Jr-Wen Shui

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 17

    Abstract: Galectins are carbohydrate binding proteins previously implicated in sensing and repairing damaged lysosomes. Here, the authors show that galectin-9 has specific lysosomal roles in autophagy and contributes to cell degeneration and apoptosis in colitis ... ...

    Abstract Galectins are carbohydrate binding proteins previously implicated in sensing and repairing damaged lysosomes. Here, the authors show that galectin-9 has specific lysosomal roles in autophagy and contributes to cell degeneration and apoptosis in colitis and pancreatitis in mice.
    Keywords Science ; Q
    Language English
    Publishing date 2020-08-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Article ; Online: Ex Vivo Expansion and Drug Sensitivity Profiling of Circulating Tumor Cells from Patients with Small Cell Lung Cancer

    Hsin-Lun Lee / Jeng-Fong Chiou / Peng-Yuan Wang / Long-Sheng Lu / Chia-Ning Shen / Han-Lin Hsu / Thierry Burnouf / Lai-Lei Ting / Pai-Chien Chou / Chi-Li Chung / Kai-Ling Lee / Her-Shyong Shiah / Yen-Lin Liu / Yin-Ju Chen

    Cancers, Vol 12, Iss 3394, p

    2020  Volume 3394

    Abstract: Small cell lung cancer (SCLC) represents one of the most aggressive malignancies among cancer types. Not only tumor sample availability is limited, but also the ability for tumor cells to rapidly acquire drug resistance are the rate-limiting bottlenecks ... ...

    Abstract Small cell lung cancer (SCLC) represents one of the most aggressive malignancies among cancer types. Not only tumor sample availability is limited, but also the ability for tumor cells to rapidly acquire drug resistance are the rate-limiting bottlenecks for overall survival in current clinical settings. A liquid biopsy capable of capturing and enriching circulating tumor cells (CTCs), together with the possibility of drug screening, is a promising solution. Here, we illustrate the development of a highly efficient ex vivo CTC expansion system based on binary colloidal crystals substrate. Clinical samples were enrolled from 22 patients with SCLC in the study. The CTCs were enriched and expanded from the collected peripheral blood samples. Expanded cells were analyzed for protein expression and observed for drug sensitivity with the use of immunofluorescence and ATP titer evaluation, respectively. Successful CTC spheroid proliferation was established after 4 weeks within 82% of all the collected peripheral blood samples from enrolled patients. Upon immunofluorescence analysis, the enriched cells showed positive markers for EpCAM, TTF-1, synaptophysin and negative for CD45. Additionally, the expanded CTCs demonstrated marked heterogeneity in the expression of E-cadherin and N-cadherin. In a preliminary case series, the drug sensitivity of patient-derived CTC to cisplatin and etoposide was studied to see the correlation with the corresponding therapeutic outcome. In conclusion, our study demonstrates that it is possible to efficiently expand CTCs from SCLC within a clinically relevant time frame; the biomarker information generated from enriched CTCs can assist the selection of effective drugs and improve disease outcome.
    Keywords small cell lung cancer ; circulating tumor cells ; primary cell culture ; liquid biopsy ; personalized medicine ; Neoplasms. Tumors. Oncology. Including cancer and carcinogens ; RC254-282
    Subject code 610
    Language English
    Publishing date 2020-11-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Lumenal Galectin-9-Lamp2 interaction regulates lysosome and autophagy to prevent pathogenesis in the intestine and pancreas

    Janaki N. Sudhakar / Hsueh-Han Lu / Hung-Yu Chiang / Ching-Shu Suen / Ming-Jing Hwang / Sung-Yu Wu / Chia-Ning Shen / Yao-Ming Chang / Fu-An Li / Fu-Tong Liu / Jr-Wen Shui

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 17

    Abstract: Galectins are carbohydrate binding proteins previously implicated in sensing and repairing damaged lysosomes. Here, the authors show that galectin-9 has specific lysosomal roles in autophagy and contributes to cell degeneration and apoptosis in colitis ... ...

    Abstract Galectins are carbohydrate binding proteins previously implicated in sensing and repairing damaged lysosomes. Here, the authors show that galectin-9 has specific lysosomal roles in autophagy and contributes to cell degeneration and apoptosis in colitis and pancreatitis in mice.
    Keywords Science ; Q
    Language English
    Publishing date 2020-08-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  9. Article: All-trans retinoic acid ameliorates glycemic control in diabetic mice via modulating pancreatic islet production of vascular endothelial growth factor-A

    Chien, Chiao-Yun / Tze-An Yuan / Candy Hsin-Hua Cho / Fang-Pei Chang / Wan-Yu Mao / Ruei-Ren Wu / Hsuan-Shu Lee / Chia-Ning Shen

    Biochemical and biophysical research communications. 2016,

    2016  

    Abstract: Patients with type 1 diabetes mellitus are associated with impairment in vitamin A metabolism. This study evaluated whether treatment with retinoic acid, the biologically active metabolite of vitamin A, can ameliorate diabetes. All-trans retinoic acid ( ... ...

    Abstract Patients with type 1 diabetes mellitus are associated with impairment in vitamin A metabolism. This study evaluated whether treatment with retinoic acid, the biologically active metabolite of vitamin A, can ameliorate diabetes. All-trans retinoic acid (atRA) was used to treat streptozotocin (STZ)-induced diabetic mice which revealed atRA administration ameliorated blood glucose levels of diabetic mice. This hyperglycemic amelioration was accompanied by an increase in the amount of β cells co-expressed Pdx1 and insulin and by restoration of the vascular laminin expression. The atRA-induced production of vascular endothelial growth factor-A from the pancreatic islets was possibly the key factor that mediated the restoration of islet vascularity and recovery of β−cell mass. Furthermore, the combination of islet transplantation and atRA administration significantly rescued hyperglycemia in diabetic mice. These findings suggest that vitamin A derivatives can potentially be used as a supplementary treatment to improve diabetes management and glycemic control.
    Keywords animal disease models ; blood glucose ; disease control ; glycemic control ; hyperglycemia ; insulin ; insulin-dependent diabetes mellitus ; islets of Langerhans ; laminin ; metabolites ; mice ; patients ; retinoic acid ; streptozotocin ; vascular endothelial growth factor A ; vitamin A ; vitamin metabolism ; All-trans retinoic acid ; Vascular endothelial growth factor ; Islet vascularization ; Type 1 diabetes mellitus ; AtRA ; STZ ; T1DM ; VEGF-A ; RAR
    Language English
    Size p. .
    Publishing place Elsevier Inc.
    Document type Article
    Note Pre-press version
    ZDB-ID 205723-2
    ISSN 0006-291X ; 0006-291X
    ISSN (online) 0006-291X
    ISSN 0006-291X
    DOI 10.1016/j.bbrc.2016.06.151
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  10. Article: Maternal vitamin A deficiency during pregnancy affects vascularized islet development

    Chien, Chiao-Yun / Candy Hsin-Hua Cho / Chia-Ning Shen / David Tosh / Hsuan-Shu Lee / Kuo-I Lin / Ruei-Ren Wu / Wan-Yu Mao

    Journal of nutritional biochemistry. 2016 Oct., v. 36

    2016  

    Abstract: Vitamin A deficiency is known to affect 20 million pregnant women worldwide. However, the prenatal effects of maternal vitamin A deficiency on pancreas development have not been clearly determined. The present study examined how maternal vitamin A ... ...

    Abstract Vitamin A deficiency is known to affect 20 million pregnant women worldwide. However, the prenatal effects of maternal vitamin A deficiency on pancreas development have not been clearly determined. The present study examined how maternal vitamin A deficiency affects fetal islet development. Vitamin A-deficient mice were generated by feeding female mice with a chemically defined diet lacking vitamin A prior to mating as well as during pregnancy. We found that maternal vitamin A deficiency during pregnancy affected fetal pancreas development. Although the exocrine differentiation appeared normal, development of islet tissue was impaired. In the pancreas of neonatal mice, only a few endocrine cell clusters were formed, and these cell clusters lacked capillary endothelial cells. To further determine how vitamin A metabolites, such as retinoic acid, regulate vascularized islet development, ex vivo culture of embryonic pancreas either in the presence of 4-diethylaminobenzaldehyde (DEAB; an inhibitor of retinaldehyde dehydrogenase), all-trans retinoic acid (atRA) or retinoic acid receptor agonist (E)-4-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylenyl)-1-propenyl] benzoic acid (TTNPB) was carried out. We found that the addition of DEAB blocked vascularization and suppressed β-cell differentiation. Conversely, atRA or TTNPB promoted β-cell differentiation accompanied by enhanced expression of vascular basement component, laminin. We further demonstrated that atRA regulated vascularization via upregulating vascular endothelial growth factor-A (VEGF-A) secretion in embryonic pancreas and treatment with VEGF-A was able to partially rescue vascularization and β-cell differentiation in DEAB-treated embryonic pancreas cultures. The findings explain why maternal vitamin A deficiency affects fetal islet development and support an essential role of retinoid signaling in regulating vascularized islet development.
    Keywords agonists ; diet ; endothelial cells ; females ; islets of Langerhans ; laminin ; maternal effect ; metabolites ; mice ; neonates ; pregnancy ; retinoic acid ; secretion ; vascular endothelial growth factor A ; vitamin A ; vitamin A deficiency
    Language English
    Dates of publication 2016-10
    Size p. 51-59.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 1014929-6
    ISSN 1873-4847 ; 0955-2863
    ISSN (online) 1873-4847
    ISSN 0955-2863
    DOI 10.1016/j.jnutbio.2016.07.010
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

To top