Pancreatic cancer (PC) remains one of the most challenging solid tumors to treat with a high unmet medical need as patients poorly respond to standard-of-care-therapies. Prominent desmoplastic reaction involving cancer-associated fibroblasts (CAFs) and the immune cells in the tumor microenvironment (TME) and their cross-talk play a significant role in tumor immune escape and progression. To identify the key cellular mechanisms induce an immunosuppressive tumor microenvironment, we established 3D co-culture model with pancreatic cancer cells, CAFs, monocyte as well as T cells. Using this model, we analysed the influence of tumor cells and fibroblasts on monocytes and their immune suppressive phenotype. Phenotypic characterization of the monocytes after 3D co-culture with tumor/fibroblast spheroids was performed by analysing the expression of defined cell surface markers and soluble factors. Functionality of these monocytes and their ability to influence T cell phenotype and proliferation was investigated. 3D co-culture of monocytes with pancreatic cancer cells and fibroblasts induced the production of immunosuppressive cytokines which are known to promote polarization of M2 like macrophages and myeloid derived suppressive cells (MDSCs). These co-culture spheroid polarized monocyte derived macrophages (MDMs) were poorly differentiated and had an M2 phenotype. The immunosuppressive function of these co-culture spheroids polarized MDMs was demonstrated by their ability to inhibit autologous CD4+ and CD8+ T cell activation and proliferation in vitro, which we could partially reverse by 3D co-culture spheroid treatment with therapeutic molecules that are able to re-activate spheroid polarized MDMs or block immune suppressive factors such as Arginase-I. In conclusion, we generated a physiologically relevant 3D co-culture model, which can be used as a promising tool to study complex cell-cell interactions between different cell types within the tumor microenvironment and to support drug screening and development. In future, research focused on better understanding of resistance mechanisms to existing cancer immunotherapies will help to develop new therapeutic strategies in order to combat cancer. / Bei Bauchspeicheldrüsenkrebs handelt es sich um eine maligne Tumorerkrankung, deren Behandlung Ärzte noch immer vor große Herausforderungen stellen und die zur dritthäufigsten krebsbedingten Todesursache der westlichen Welt zählt. Desmoplastische Reaktionen im Tumorgewebe sind hierbei ein besonderes Merkmal dieser Erkrankung. Dabei spielen tumor-assoziierte Fibroblasten sowie unterschiedliche Zellen des Immunsystems und deren Interaktionen eine essentielle Rolle hinsichtlich Tumorwachstum und der Herunterregulation des Immunsystems. Um zelluläre Mechanismen, die ein immunsuppressives Tumormilieu induzieren, zu identifizieren, entwickelten wir ein 3D Ko-Kultur Modell mit Bauchspeicheldrüsenkrebszellen, tumor-assoziierten Fibroblasten sowie Monozyten und T-Zellen. Mit Hilfe dieses Modells konnten wir den Einfluss von Tumorzellen und Fibroblasten auf den Phänotyp und das Verhalten von Monozyten untersuchen. Dazu wurden Monozyten in einer 3D Tumorzell/Fibroblasten Ko-Kultur kultiviert und differenziert, um anschließend die Expression definierter Zelloberflächenmarker und löslicher Faktoren zu analysieren. Des Weiteren wurde das Verhalten dieser 3D Ko-Kultur differenzierten myeloiden Zellpopulation sowie ihre Fähigkeit den Phänotyp von T Zellen und deren Proliferation zu beeinflussen untersucht. Die 3D Ko-Kultur der Monozyten zusammen mit den Tumorzellen und den Fibroblasten führten zur Produktion immunsuppressiver Zytokine und Chemokine, wodurch die Differenzierung der Monozyten in M2-ähnliche Makrophagen induziert wurde. Diese durch die 3D Tumorzell/Fibroblasten Sphäroide polarisierten aus Monozyten herangereiften M2-ähnlichen Makrophagen besaßen außerdem immunsuppressive funktionelle Eigenschaften, indem sie in der Lage waren, die Aktivierung und Proliferation von autologen CD4+ und CD8+ T Zellen in vitro zu inhibieren. Die Suppression sowohl der CD4+ als auch der CD8+ T Zellen konnte durch die Behandlung therapeutischer Moleküle, die die Re-Aktivierung der immunsuppressiven 3D Sphäroid polarisierten Makrophagen stimulierten oder suppressive Faktoren wie Arginase-I blockierten, wieder aufgehoben und die T Zell Proliferation teilweise wiederhergestellt werden. Unser etabliertes 3D Ko-Kultur System repräsentiert ein vielversprechendes physiologisch relevantes Modell, welches genutzt werden kann, um Zell-Zell Interaktion und Kommunikation im Tumormilieu zu untersuchen und dadurch die Wirkung von Medikamenten zu verbessern. Ein gezieltes besseres Verständnis von Tumorresistenz Mechanismen gegen bereits bestehende Immun Therapien fördert die Entwicklung neuer therapeutischer Ansätze zur Bekämpfung von Krebs.

The formation of synapses in cell cultures of rat cerebellum was examined in the presence of the protein synthesis inhibitor cycloheximide. First, cell survival in the presence of 25 μg/ml cycloheximide was determined by phase contrast microscopy, trypan blue exclusion, total protein and uptake of [3H]gamma-aminobutyric acid (GABA). Neurons with 24 h incubation in cycloheximide appeared normal with little cell death, but by 48 h incubation the first signs of cell death were found. Some viable neurons were still found in cultures incubated continuously in cycloheximide for 72 h. Normally, the number of synapses seen in cerebellar cultures with the electron microscope shows an increase during the first several weeks in culture. However, the number of synapses in cultures treated with cycloheximide decreased, indicating that inhibition of protein synthesis at least partially inhibited synaptogenesis. Cycloheximide also inhibited the maintenance of synapses already formed as seen by the decrease in the number of synapses from the time the cycloheximide was added. To determine the sensitivity of the forming presynaptic element to cycloheximide, the development of apparent presynaptic elements was investigated. In cultures treated with polylysine-coated sepharose beads, neurites grew and formed apparent presynaptic elements with the bead taking the position of the postsynaptic element. Cultures pretreated with cycloheximide for 1 h followed by 24 h incubation with both cycloheximide and coated beads showed a normal number of apparent presynaptic elements. The first decrease in numbers was seen after 12 h preincubation and 12 h incubation with both cycloheximide and coated beads. Even after 72 h continuous incubation some apparent presynaptic elements could be formed although at reduced levels. Results presented here suggest that continuous protein synthesis is not necessary for the formation of the presynaptic element, but that active protein synthesis is required for neurons to form and maintain postsynaptic elements.

Intervertebral disc (IVD) degeneration is a prevalent health problem that is highly linked to back pain. To understand the disease and tissue response to therapies, ex-vivo whole IVD organ culture systems have recently been introduced. The goal of this study was to develop and validate a whole spinal segment culturing system that loads the disc in complex loading similar to the in-vivo condition, while preserving the adjacent endplates and vertebral bodies. The complex loading applied to the spinal segment was achieved with three pneumatic cylinders. The pneumatic cylinders were rigidly attached to two triangular alumni plates at each corner, comprising the loading mechanism. By extending or compressing the pneumatic cylinders, three modes of loading were achieved: flexion-extension, bi-lateral bending, and cyclic compression. The cylinders were controlled via microcontroller, and the entire system was fully automated. The culture container, which housed the spinal segment during culturing, was a flexible silicone container with an aluminum base and lid. The culture container attached to the loading mechanism allows for loading of the spinal segment. It had a vent attached to the aluminum lid that allowed for gas exchange in the system. The dynamic bioreactor was able to achieve physiologic loading conditions with 100 N of applied compression and approximately 2-4 N-m of applied torque. The function of the bioreactor was validated through testing of bovine caudal IVDs with intact endplates and vertebral bodies that were isolated within 2 hours of death and cultured for 14 days under a diurnal cycle. The resulting IVD cell viability following 14 days of loading was approximately 43% and 20% for the nucleus pulposus and annulus fibrosus respectively, which was significantly higher than the unloaded controls. The loading system accurately mimicked flexion-extension, bi-lateral bending, and compression motions seen during daily activities. Results indicate that this complex dynamic bioreactor may be appropriate for extended pre-clinical testing of vertebral mounted spinal devices and therapies.

Putrescine, spermidine and spermine are classified as polyamines and are found in virtually all living tissues. Although polyamines have been proposed to influence cell proliferation and differentiation, the mechanism by which they do so is not well understood. Previous studies in our laboratory have been focused on the interconversion of spermidine and N8-acetylspermidine (N8-AcSpd) and the enzyme N8-AcSpd deacetylase. In the present study, a N8-AcSpd deacetylase inhibitor, 7-[N-(3-aminopropyl) amino] heptan-2-one (APAH) was employed to study the effect of N8-AcSpd deacetylase inhibition on proliferation of cultured cells. This study for the first time shows the pharmacological effects of elevated N8-AcSpd levels and inhibition of N8-AcSpd deacetylation. Based on the fact that inhibition of N8-AcSpd deacetylation stimulates the growth of cells in culture, we propose to search for a new class of antitumor agents among the inhibitors of spermidine N8-acetyltransferase.

The ability to inject DNA and other foreign particles into cells, both germ cells (e.g. to produce transgenic animals) and somatic cells (e.g. for gene therapy), is a powerful tool in genetic research. Nanoinjection is a method of DNA delivery that combines mechanical and electrical methods. It has proven to have higher cell viability than traditional microinjection, resulting in higher integration per injected embryo. The nanoinjection process can be performed on thousands of cells simultaneously using an array of microneedles that is inserted into a monolayer of cells. This thesis describes the needle array design requirements and the fabrication process used to meet them. The process uses unpassivated and passivated deep reactive ion etching (DRIE) to create needles with a constant diameter shaft and a pointed tip. The needle diameter and height are about 1 µm and 8 µm, respectively. A buckling analysis and physical testing show that the needles can withstand the force required to penetrate the cells. The chip is attached to a plastic suspension with a counter electrode and electrical connections to a voltage source. The suspension's motion is defined by two compliant orthoplanar springs that have been vertically and rotationally offset for added stability. The base of the suspension is designed to exactly fit in the bottom of a cell culture dish, where the needle array can be pushed into the cell monolayer. Injection protocol was created and followed to perform tests with needle insertion only, voltage application only, and the full nanoinjection process. The average cell viability for the full injection process was 98.2% compared to an average control viability of 99.5%. Zero volt injections with a high concentration of propidium iodide, a cell impermeable dye with two positive charges, resulted in dye uptake from diffusion, proving that the needles are penetrating the cells. Tests comparing injections with and without voltage had high variability in dye uptake. Therefore, glass cover slips were placed in the culture dishes to provide more consistent injection conditions. This reduced variation in zero voltage tests. It is recommended that this procedure be followed for performing injections with voltage.

Hydrogels are high water-content polymers that mimic the extracellular matrix of cells. The polymers can have many sources and be of natural origin from the extracellular matrix (ECM) of cells or be synthetically derived. Two such polymers are hyaluronic acid and gelatin, which can with the help of the release of free radicals from photoinitiators, initiated by UV light, polymerise, and form a hydrogel. In these hydrogels, cells can be encapsulated. The hydrogels can in turn be used to maintain cells as they are in the natural environment. For example, hydrogels can provide an in-vivo-like ECM for stem cells and endothelial cells by supporting “stemness” and cell-to-cell contact; respectively. We aim to establish a protocol for culturing cells in the hydrogelas a first milestone in a project focused on profiling the metabolome of cells grown in hydrogels. To accomplish this, four types of cells, namely mouse brain microvascular endothelial cells (bEnd.3), human umbilical vein endothelial cells (HUVECs), adult human lung fibroblast (hLFs) and mesenchymal stem cells (MSCs), were evaluated for growth in hyaluronic acid methacrylate (HA-ma), hyaluronic acid acrylamide (HA-am) as well as a QuattroGel composed by gelatin methacryloyl (GelMA), HA-ma, fibrinogen and thrombin. It was found that HA-masupported viability and the stemness of mesenchymal stem cells, of which the metabolome can be further studied in order to evaluate the difference between regular 2D maintenance and maintenance in 3D. No sprouting was observed for the other cells encapsulated in the hydrogel, and further experiments are needed to find the source of error.

Human society has benefited greatly from plant secondary metabolites, often utilizing a variety of compounds as dyes, food additives, and drugs. In particular, pharmaceutical development has benefited greatly from plant secondary metabolites. One example of this utility is paclitaxel, a highly substituted diterpene approved in the treatment of breast cancer, ovarian cancer, non-small cell lung cancer, and the AIDSrelated Kaposi’s sarcoma. Demand of paclitaxel is likely to increase, due to the current examination of paclitaxel in numerous clinical trials against a variety of other cancers. Taxus cell culture represents a production source of paclitaxel to meet future demand. However, paclitaxel production through Taxus cell culture is often variable and low. Targeted metabolic engineering of Taxus to produce superior paclitaxelaccumulating lines is a viable strategy to address variable and low yields. To facilitate the production of genetically engineered Taxus cell lines, stable transformation is required to examine the long-term effect of gene expression in vitro. Additionally, suitable transient transformation systems are necessary to characterize novel Taxus genes related to paclitaxel accumulation. A transient particle bombardment-mediated transformation protocol was developed to introduce transgenes into Taxus cells in vitro. Additionally, agroinfiltration in Nicotiana benthamiana was examined as a system to express genes related to paclitaxel biosynthesis and lead to the accumulation of the first dedicated taxane, taxa- 4(5), 11(12)-diene. In regard to stable transformation, an Agrobacterium-mediated transformation protocol was developed, though this method requires further optimization for reliability and increased transformation efficiency. These transformation technologies will aid in the creation of elite paclitaxel-accumulating Taxus cell lines.

The use of nanowires, nano and micro needles in biomedical applications has markedly increased in the past years, mainly due to attractive properties such as biocompatibility and simple fabrication. Specifically, these structures have shown promise in applications including cell separation, tumor cell capture, intracellular delivery, cell therapy, cancer treatment and as cell growth scaffolds. The work proposed here aims to study two platforms for different applications: a vertical magnetic nanowire array for mesenchymal stem cell differentiation and a micro needle platform for intracellular delivery. First, a thorough evaluation of the cytotoxicity of nanowires was done in order to understand how a biological system interacts with high aspect ratio structures. Nanowires were fabricated through pulsed electrodeposition and characterized by electron microscopy, vibrating sample magnetometry and energy dispersive X-ray spectroscopy. Studies of biocompatibility, cell death, cell membrane integrity, nanowire internalization and intracellular dissolution were all performed in order to characterize the cell response. Results showed a variable biocompatibility depending on nanowire concentration and incubation time, with cell death resulting from an apoptotic pathway arising after internalization. A vertical array of nanowires was then used as a scaffold for the differentiation of human mesenchymal stem cells. Using fluorescence and electron microscopy, the interactions between the dense array of nanowires and the cells were analyzed, as well as the biocompatibility of the array and its effects on cell differentiation. A magnetic field was additionally applied on the substrate to observe a possible differentiation. Stem cells grown on this scaffold showed a cytoskeleton and focal adhesion reorganization, and later expressed the osteogenic marker osteopontin. The application of a magnetic field counteracted this outcome. Lastly, a micro needle platform was fabricated through lithography and electrodeposition, characterized using the previously mentioned techniques and then evaluated as a vector for intracellular delivery. Fluorescence and electron microscopy imaging were first performed to assess the biocompatibility, cell spreading and the interface of the cells and the needles. Intracellular delivery of a fluorescent dye was achieved via inductive heating of the needles, with the results showing a dependency of delivery and cell survivability on the exposure time.

Orthopedic metal implant materials may mediate a variety of adverse tissue reactions by releasing ions through corrosion. Adverse tissue reactions include inflammation, fibrosis and hypersensitivity. All of these reactions eventually lead to implant failure. The goal of this study was to provide a better understanding of the cellular-material interaction at the metal surface. The hypotheses were that 1. the attachment of cells and their released reactive inflammatory compounds (e.g. hydrogen peroxide H2O2, superoxide O2. and nitric oxide NO.) on the surfaces alter the alloys? corrosion and surface properties and 2. the changes in corrosion and chemical properties of the surfaces affect cell behavior. To evaluate the hypotheses, a custom-made electrochemical corrosion cell was used to evaluate how cell culture medium, macrophage cells and macrophage cells activated to simulate inflammation affected the corrosion and surface properties of Co-Cr-Mo and Ti-6Al-4V alloys and how released alloy corrosion products affected cell behaviors. The macrophage cell line used was known to produce reactive species H2O2, O2. and NO. when activated by antigen and interferon. The alloy corrosion properties were enhanced by observing the open circuit potential (OCP), charge transfer, metal ion release, and changes in surface oxides. Proliferation, viability and metabolism were used to evaluate effects of corrosion on the cells. The OCP of Co-Cr-Mo remained unchanged whereas that of Ti-6Al-4V increased over three days for all three test conditions. Both alloys cultured with medium had the lowest OCP among all conditions. With activated macrophage cells, both alloys had the lowest total charge transfer and concentrations of metal ion released. This improved corrosion resistance was mostly due to an enhancement of the surface oxide due to the reactive species released from activated cells, as indicated from the surface analyses. Both alloys were found to have increased percentage (in peak intensity) of O and Ti or Cr peaks, which indicated an increase of Ti and Cr oxides on Ti-6Al-4V and Co-Cr-Mo alloys respectively. The improved corrosion properties resulted in less metal ion release than those without enhanced surface oxides, thus alloys did not further activate cell immune responses in the three day period. The non-activated or activated cells with released metal ions did not exhibit any degradation in their viability, intracellular ATP, NO and IL-1b release as compared to controls. This is consistent with the generally accepted good biocompatibility of these alloys.

No description available.