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Scalable Production of Equine Platelet Lysate for Multipotent Mesenchymal Stromal Cell CultureHagen, A., Lehmann, H., Aurich, S., Bauer, N., Melzer, M., Moellerberndt, J., Patané, V., Schnabel, C.L., Burk, J. 03 April 2023 (has links)
Translation of multipotent mesenchymal stromal cell (MSC)-based therapies is advancing
in human and veterinary medicine. One critical issue is the in vitro culture of MSC before
clinical use. Using fetal bovine serum (FBS) as supplement to the basal medium is still the
gold standard for cultivation of many cell types including equine MSC. Alternatives are
being explored, with substantial success using platelet lysate-supplemented media for
human MSC. However, progress lags behind in the veterinary field. The aim of this study
was to establish a scalable protocol for equine platelet lysate (ePL) production and to test
the ePL in equine MSC culture. Whole blood was harvested into blood collection bags
from 20 healthy horses. After checking sample materials for pathogen contamination,
samples from 19 animals were included. Platelet concentrates were prepared using a
buffy coat method. Platelets, platelet-derived growth factor BB, and transforming growth
factor b1 concentrations were increased in the concentrates compared with whole blood
or serum (p < 0.05), while white blood cells were reduced (p < 0.05). The concentrates
were lysed using freeze/thaw cycles, which eliminated the cells while growth factor
concentrations were maintained. Donor age negatively correlated with platelet and
growth factor concentrations after processing (p < 0.05). Finally, all lysates were pooled
and the ePL was evaluated as culture medium supplement in comparison with FBS,
using adipose-derived MSC from four unrelated donor horses. MSC proliferated well
in 10% FBS as well as in 10% ePL. However, using 5 or 2.5% ePL entailed highly
inconsistent proliferation or loss of proliferation, with significant differences in generation
times and confluencies (p < 0.05). MSC expressed the surface antigens CD90, CD44,
and CD29, but CD73 and CD105 detection was low in all culture media. Adipogenic
and osteogenic differentiation led to similar results in MSC from different culture media.
The buffy coat method is useful to produce equine platelet concentrate with increased
platelet and reduced white blood cell content in large scales. The ePL obtained supports
MSC expansion similar as FBS when used at the same concentration (10%). Further
investigations into equine MSC functionality in culture with ePL should follow.
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Phospholipid Profiles for Phenotypic Characterization of Adipose-Derived Multipotent Mesenchymal Stromal CellsBurk, Janina, Melzer, Michaela, Hagen, Alina, Lips, Katrin Susanne, Trinkaus, Katja, Nimptsch, Ariane, Leopold, Jenny 03 April 2023 (has links)
Multipotent mesenchymal stromal cells (MSC) have emerged as therapeutic tools for a
wide range of pathological conditions. Yet, the still existing deficits regarding MSC
phenotype characterization and the resulting heterogeneity of MSC used in different
preclinical and clinical studies hamper the translational success. In search for novel
MSC characterization approaches to complement the traditional trilineage
differentiation and immunophenotyping assays reliably across species and culture
conditions, this study explored the applicability of lipid phenotyping for MSC
characterization and discrimination. Human peripheral blood mononuclear cells
(PBMC), human fibroblasts, and human and equine adipose-derived MSC were used
to compare different mesodermal cell types and MSC from different species. For MSC,
cells cultured in different conditions, including medium supplementation with either fetal
bovine serum or platelet lysate as well as culture on collagen-coated dishes, were
additionally investigated. After cell harvest, lipids were extracted by chloroform/
methanol according to Bligh and Dyer. The lipid profiles were analysed by an
untargeted approach using liquid chromatography coupled to mass spectrometry (LCMS)
with a reversed phase column and an ion trap mass spectrometer. In all samples,
phospholipids and sphingomyelins were found, while other lipids were not detected with
the current approach. The phospholipids included different species of phosphatidylcholine
(PC), phosphatidylethanolamine (PE), phosphatidylinositol (PI) and phosphatidylserine (PS)
in all cell types, whereas phosphatidylglycerol (PG) species were only present in MSC.
MSC from both species showed a higher phospholipid species diversity than PBMC and
fibroblasts. Few differences were found between MSC from different culture conditions,
except that human MSC cultured with platelet lysate exhibited a unique phenotype in that
they exclusively featured PE O-40:4, PG 38:6 and PG 40:6. In search for specific and
inclusive candidate MSC lipid markers, we identified PE O-36:3 and PG 40:7 as potentially
suitable markers across culture conditions, at which PE O-36:3 might even be used across
species. On that basis, phospholipid phenotyping is a highly promising approach for MSC
characterization, which might condone some heterogeneity within the MSC while still
achieving a clear discrimination even from fibroblasts. Particularly the presence or absence
of PG might emerge as a decisive criterion for future MSC characterization.
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Combined Experimental and Mathematical Approach for Development of a Microfabrication-Based Model to Investigate Cell-Cell Interaction during MigrationSarkar, Saheli 30 March 2011 (has links)
No description available.
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Prevention of Incisional Hernias Using Mesenchymal Stromal Cells and Platelet-Rich Plasma treated Collagen Matrix TapeDiehl, Michael W. 18 June 2014 (has links)
No description available.
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The Utilization of Multipotent Mesenchymal Stromal Cell Transplantation to Improve Fascia RepairBown, Andre B. J. 19 September 2013 (has links)
No description available.
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T-ALL LEUKEMIA DYSREGULATES STROMAL BONE MARROW ENVIRONMENT AND DISRUPTS NICHE-STEM CELL SIGNALING AXISZimmerman, Grant Robert 03 September 2015 (has links)
No description available.
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Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice / iPS細胞由来間葉系間質細胞の新生仔投与による全身性の6型コラーゲン補充は、6型コラーゲン欠損モデルマウスの組織学的特徴および運動機能を改善するHarada, Aya 23 March 2022 (has links)
京都大学 / 新制・課程博士 / 博士(医学) / 甲第23770号 / 医博第4816号 / 新制||医||1056(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 長船 健二, 教授 安達 泰治, 教授 遊佐 宏介 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
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Selective vulnerability of human-induced pluripotent stem cells to dihydroorotate dehydrogenase inhibition during mesenchymal stem/stromal cell purification / ジヒドロオロト酸デヒドロゲナーゼ阻害剤による間葉系幹/間質細胞からの未分化iPS細胞の選択的除去Ziadoon, Hameed Abed Al-Akashi 25 March 2024 (has links)
京都大学 / 新制・課程博士 / 博士(医学) / 甲第25197号 / 医博第5083号 / 京都大学大学院医学研究科医学専攻 / (主査)教授 齋藤 潤, 教授 斎藤 通紀, 教授 長船 健二 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
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Towards the development of vascularized constructs for bone repairChang-Wai-Ling, Nolanne Arlette January 2013 (has links)
The development of a vasculature within a tissue-engineered construct is one of the largest hurdles to successful bone regeneration. This thesis investigates methods to increase vasculature of such transplanted constructs, based on in vivo transplant studies and in vitro analysis of cell behaviors. A syngeneic mouse model in immunocompetent mice was developed and analyzed for both osteogenesis and hematopoiesis. This study demonstrates that syngeneic bone marrow stromal cells (BMSCs) are not rejected by the host, provided the strain of mice is sufficiently inbred. Additionally, an effective protocol was developed for the isolation of endothelial cells (ECs) from the bone marrow of mice. Two different sets of materials for this study were analyzed, both collagen based, and the GelfoamTM scaffold was found to possess advantages over synthesized collagen or collagen/hydroxyapatite composites, although only for mouse and not human bone transplantation. In order to gain rapid and integrated vasculature formation within the transplant, attempts were made to increase both (de novo) vasculogenesis and angiogenesis (ingrowth) from the surrounding tissue. For the former, transplant studies were combined with in vitro osteogenic calcification studies. Direct co-culture of the BMSCs and ECs increased osteogenic calcification and was monitored by using both alizarin red S quantification and quantitative polymerase chain reaction. Angiogenesis (as assessed by cell migration) was studied by various motility and chemotaxis assays in vitro, as well as through use of a directed in vivo angiogenesis assay. Growth factors, particularly TGF-β1 and BMP-4, were found to increase cell movement in these systems. In conclusion, we show that although much work remains to be done in order to increase the vasculature in bone transplants, systematic combination of in vivo and in vitro assays can elucidate the nature behind this crucial process in this context.
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Adipose-derived human stem/stromal cells: comparative organ specific mitochondrial bioenergy profilesFerng, Alice S., Marsh, Katherine M., Fleming, Jamie M., Conway, Renee F., Schipper, David, Bajaj, Naing, Connell, Alana M., Pilikian, Tia, Johnson, Kitsie, Runyan, Ray, Black, Stephen M., Szivek, John A., Khalpey, Zain 01 December 2016 (has links)
Background: Adipose-derived stem/stromal cells (ASCs) isolated from the stromal vascular fraction are a source of mesenchymal stem cells that have been shown to be beneficial in many regenerative medicine applications. ASCs are an attractive source of stem cells in particular, due to their lack of immunogenicity. This study examines differences between mitochondrial bioenergetic profiles of ASCs isolated from adipose tissue of five peri-organ regions: pericardial, thymic, knee, shoulder, and abdomen. Results: Flow cytometry showed that the majority of each ASC population isolated from the adipose tissue of 12 donors, with an n = 3 for each tissue type, were positive for MSC markers CD90, CD73, and CD105, and negative for hematopoietic markers CD34, CD11B, CD19, and CD45. Bioenergetic profiles were obtained for ASCs with an n = 4 for each tissue type and graphed together for comparison. Mitochondrial stress tests provided the following measurements: basal respiration rate (measured as oxygen consumption rate [pmol O-2/min], ATP production, proton leak, maximal respiration, respiratory control ratio, coupling efficiency, and non-mitochondrial respiration. Glycolytic stress tests provided the following measurements: basal glycolysis rate (measured as extracellular acidification rate [mpH/min]), glycolytic capacity, glycolytic reserve, and non-glycolytic acidification. Conclusions: The main goal of this manuscript was to provide baseline reference values for future experiments and to compare bioenergetic potentials of ASCs isolated from adipose tissue harvested from different anatomical locations. Through an investigation of mitochondrial respiration and glycolysis, it was demonstrated that bioenergetic profiles do not significantly differ by region due to depot-dependent and donor-dependent variability. Thus, although the physiological function, microenvironment and anatomical harvest site may directly affect the characteristics of ASCs isolated from different organ regions, the ultimate utility of ASCs remains independent of the anatomical harvest site.
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