scholarly journals Development of an in vitro model to study the impact of BMP-2 on metastasis to bone

2010 ◽  
Vol 4 (8) ◽  
pp. 590-599 ◽  
Author(s):  
Heenam Kwon ◽  
Hyeon Joo Kim ◽  
William L. Rice ◽  
Balajikarthick Subramanian ◽  
Sang-Hyug Park ◽  
...  
Keyword(s):  
In Vitro Model ◽  
Vitro Model ◽  
The Impact

scholarly journals CAFs affect the proliferation and treatment response of head and neck cancer spheroids during co-culturing in a unique in vitro model

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Mustafa Magan ◽  
Emilia Wiechec ◽  
Karin Roberg
Keyword(s):  
Cell Proliferation ◽  
Tumor Cell ◽  
Head And Neck ◽  
Treatment Response ◽  
Tumor Cells ◽  
In Vitro Model ◽  
Tumor Spheroids ◽  
Vitro Model ◽  
The Impact

Abstract Background Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous group of tumors for which the overall survival rate worldwide is around 60%. The tumor microenvironment, including cancer-associated fibroblasts (CAFs), is believed to affect the treatment response and migration of HNSCC. The aim of this study was to create a biologically relevant HNSCC in vitro model consisting of both tumor cells and CAFs cultured in 3D to establish predictive biomarkers for treatment response, as well as to investigate the impact of CAFs on phenotype, proliferation and treatment response in HNSCC cells. Methods Three different HNSCC patient-derived tumor cell lines were cultured with and without CAFs in a 3D model. Immunohistochemistry of the proliferation marker Ki67, epidermal growth factor receptor (EGFR) and fibronectin and a TUNEL-assay were performed to analyze the effect of CAFs on both tumor cell proliferation and response to cisplatin and cetuximab treatment in tumor spheroids (3D). mRNA expression of epithelial-mesenchymal transition (EMT) and cancer stem cells markers were analyzed using qRT-PCR. Results The results demonstrated increased cell proliferation within the tumor spheroids in the presence of CAFs, correlating with increased expression of EGFR. In spheroids with increased expression of EGFR, a potentiated response to cetuximab treatment was observed. Surprisingly, an increase in Ki67 expressing tumor cells were observed in spheroids treated with cisplatin for 3 days, correlating with increased expression of EGFR. Furthermore, tumor cells co-cultured with CAFs presented an increased EMT phenotype compared to tumor cells cultured alone in 3D. Conclusion Taken together, our results reveal increased cell proliferation and elevated expression of EGFR in HNSCC tumor spheroids in the presence of CAFs. These results, together with the altered EMT phenotype, may influence the response to cetuximab or cisplatin treatment.

Influence of Bacillus subtilis C-3102 on microbiota in a dynamic in vitro model of the gastrointestinal tract simulating human conditions

2012 ◽  
Vol 3 (3) ◽  
pp. 229-236 ◽  
Author(s):  
M. Hatanaka ◽  
Y. Nakamura ◽  
A.J.H. Maathuis ◽  
K. Venema ◽  
I. Murota ◽  
...  
Keyword(s):  
Bacillus Subtilis ◽  
Gastrointestinal Tract ◽  
In Vitro Model ◽  
Germination Rate ◽  
Human Colon ◽  
Micro Array ◽  
Vitro Model ◽  
Oral Doses ◽  
The Impact

Survival and germination rate of Bacillus subtilis C-3102 spores were investigated in a stomach and small intestine model (TIM-1), while the impact of C-3102 cells that had passed through TIM-1 on human colon microbiota was evaluated in a model of the large intestine (TIM-2). The survival of C-3102 spores in TIM-1 was 99%; 8% of the spores had germinated. Effluent of TIM-1 was subsequently introduced into TIM-2 and a micro-array platform was employed to assess changes in the microbiota composition. The effluent, which contained germinated C-3102 cells, increased some Bifidobacterium species and decreased some Clostridium groups. These changes were greater compared to those obtained by adding C-3102 spores directly to TIM-2. The present study suggests that oral doses of B. subtilis C-3102 spores have the potential to modulate the human colon microbiota. This effect may be caused by germination of the spores in the gastrointestinal tract.

scholarly journals An in vitro model to evaluate the impact of environmental fine particles (PM0.3-2.5) on skin damage

2019 ◽  
Vol 305 ◽  
pp. 94-102 ◽  
Author(s):  
Anthony Verdin ◽  
Fabrice Cazier ◽  
Richard Fitoussi ◽  
Natacha Blanchet ◽  
Katell Vié ◽  
...  
Keyword(s):  
In Vitro Model ◽  
Fine Particles ◽  
Skin Damage ◽  
Vitro Model ◽  
The Impact

scholarly journals 1820P Taxane-related skin toxicity: Analysis of an in vivo and 3D in vitro model study of the impact of paclitaxel on skin

2020 ◽  
Vol 31 ◽  
pp. S1050
Author(s):  
M. Perez-Leal ◽  
J.A. Perez Fidalgo ◽  
C. Sanz ◽  
J. Poveda ◽  
J. Milara ◽  
...  
Keyword(s):  
In Vitro Model ◽  
Skin Toxicity ◽  
Model Study ◽  
3D In Vitro Model ◽  
Toxicity Analysis ◽  
Vitro Model ◽  
The Impact

Spinal cord–fragment interactions following burst fracture: an in vitro model

2006 ◽  
Vol 5 (3) ◽  
pp. 243-250 ◽  
Author(s):  
Richard M. Hall ◽  
Robert J. Oakland ◽  
Ruth K. Wilcox ◽  
David C. Barton
Keyword(s):  
Spinal Cord ◽  
High Speed ◽  
In Vitro Model ◽  
Burst Fracture ◽  
Posterior Longitudinal Ligament ◽  
Bone Fragment ◽  
The Status ◽  
Vitro Model ◽  
The Impact

Object The purpose of the study was to develop an in vitro model of the bone fragment and spinal cord interactions that occur during a burst fracture and further the understanding of how the velocity of the bone fragment and the status of the posterior longitudinal ligament (PLL) affect the deformation of the cord. Methods An in vitro model was developed such that high-speed video and pressure measurements recorded the impact of a simulated bone fragment on sections of explanted bovine spinal cord. The model simulated the PLL and the posterior elements. The status of the PLL had a significant effect on both the maximum occlusion of the spinal cord and the time for occlusion to occur. Raising the fragment velocity led to an overall increase in the spinal cord deformation. Interestingly the dura mater appeared to have little or no effect on the extent of occlusion. Conclusions These findings may indicate the importance of the dura’s interaction with the cerebrospinal fluid in protecting the cord during this type of impact.

scholarly journals Rituximab Treatment in Hepatitis C Infection: An In Vitro Model to Study the Impact of B Cell Depletion on Virus Infectivity

PLoS ONE ◽  
2011 ◽  
Vol 6 (9) ◽  
pp. e25789 ◽  
Author(s):  
Zania Stamataki ◽  
Samantha Tilakaratne ◽  
David H. Adams ◽  
Jane A. McKeating
Keyword(s):  
Hepatitis C ◽  
B Cell ◽  
In Vitro Model ◽  
Cell Depletion ◽  
Virus Infectivity ◽  
B Cell Depletion ◽  
Hepatitis C Infection ◽  
Vitro Model ◽  
The Impact

scholarly journals Adaptation of Staphylococcus aureus in a Medium Mimicking a Diabetic Foot Environment

Toxins ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 230
Author(s):  
Cassandra Pouget ◽  
Claude-Alexandre Gustave ◽  
Christelle Ngba-Essebe ◽  
Frédéric Laurent ◽  
Emmanuel Lemichez ◽  
...  
Keyword(s):  
Staphylococcus Aureus ◽  
Diabetic Foot ◽  
In Vitro Model ◽  
Virulence Genes ◽  
Chronic Wounds ◽  
Ring Test ◽  
Vitro Model ◽  
The Impact

Staphylococcus aureus is the most prevalent pathogen isolated from diabetic foot infections (DFIs). The purpose of this study was to evaluate its behavior in an in vitro model mimicking the conditions encountered in DFI. Four clinical S. aureus strains were cultivated for 16 weeks in a specific environment based on the wound-like medium biofilm model. The adaptation of isolates was evaluated as follows: by Caenorhabditis elegans model (to evaluate virulence); by quantitative Reverse Transcription-Polymerase Chain Reaction (qRT-PCR) (to evaluate expression of the main virulence genes); and by Biofilm Ring test® (to assess the biofilm formation). After 16 weeks, the four S. aureus had adapted their metabolism, with the development of small colony variants and the loss of b-hemolysin expression. The in vivo nematode model suggested a decrease of virulence, confirmed by qRT-PCRs, showing a significant decrease of expression of the main staphylococcal virulence genes tested, notably the toxin-encoding genes. An increased expression of genes involved in adhesion and biofilm was noted. Our data based on an in vitro model confirm the impact of environment on the adaptation switch of S. aureus to prolonged stress environmental conditions. These results contribute to explore and characterize the virulence of S. aureus in chronic wounds.

scholarly journals Rhinovirus C replication is associated with the endoplasmic reticulum and triggers cytopathic effects in an in vitro model of human airway epithelium

2021 ◽  
Author(s):  
Talita B Gagliardi ◽  
Monty E Goldstein ◽  
Daniel Song ◽  
Kelsey M Gray ◽  
Jae W Jung ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
Airway Epithelium ◽  
In Vitro Model ◽  
Cytopathic Effects ◽  
Human Airway ◽  
Human Airway Epithelium ◽  
Vitro Model ◽  
Rhinovirus C ◽  
The Impact

The clinical impact of rhinovirus C (RV-C) is well-documented; yet the viral life cycle remains poorly defined. Thus, we characterized RV-C15 replication at the single-cell level and its impact on the human airway epithelium (HAE) using a physiologically-relevant in vitro model. RV-C15 replication was restricted to ciliated cells where viral RNA levels peaked at 12 hours post-infection (hpi), correlating with elevated titers in the apical compartment at 24 hpi. Notably, infection was associated with a loss of polarized expression of the RV-C receptor, cadherin-related family member 3. Visualization of double-stranded RNA (dsRNA) during RV-C15 replication revealed two distinct replication complex arrangements within the cell, likely corresponding to different time points in infection and correlating with the formation of large intracellular vesicles. To further define RV-C15 replication sites, we analyzed the expression of giantin, phosphatidylinositol-4-phosphate, and calnexin, as well as the colocalization of these markers with dsRNA. Fluorescence levels of all three cellular markers were elevated during infection and altered giantin distribution further indicated Golgi fragmentation. However, unlike previously characterized RVs, the high ratio of calnexin-dsRNA colocalization implicated the endoplasmic reticulum as the primary site for RV-C15 replication in HAE. RV-C15 infection was also associated with elevated stimulator of interferon genes (STING) expression, facilitating replication, and the induction of incomplete autophagy, a mechanism used by other RVs to promote non-lytic release of progeny virions. Finally, RV-C15 infection resulted in a temporary loss in epithelial barrier integrity and the translocation of tight junction proteins while a reduction in mucociliary clearance indicated cytopathic effects on epithelial function. Together, our findings identify both shared and unique features of RV-C replication compared to related rhinoviruses and define the impact of RV-C on both epithelial cell organization and tissue functionality - aspects of infection that may contribute to pathogenesis in vivo.

An in vitro model to assess the impact on respiratory cells of air pollutants

2009 ◽  
Vol 189 ◽  
pp. S86
Author(s):  
Charles Persoz ◽  
Christopher Leleu ◽  
Sophie Achard ◽  
Isabelle Momas ◽  
Nathalie Seta
Keyword(s):  
Air Pollutants ◽  
In Vitro Model ◽  
Respiratory Cells ◽  
Vitro Model ◽  
The Impact

An in vitro model to assess the impact of lipid on the rate and extent of fibre degradation

2002 ◽  
Vol 2002 ◽  
pp. 170-170 ◽  
Author(s):  
F.L. Mould ◽  
K.J. Shingfield ◽  
C.K. Reynolds ◽  
A.S. Grandison
Keyword(s):  
In Vitro Model ◽  
Energy Content ◽  
Fats And Oils ◽  
Current Data ◽  
Dietary Energy ◽  
Fibre Degradation ◽  
Low Levels ◽  
Vitro Model ◽  
The Impact

Although high genetic merit dairy cows are capable of peak yields in excess of 50 kg per day these are seldom maintained primarily due to an inability to satisfy energy requirements. Fats and oils are often incorporated into rations as a means of increasing dietary energy content. However, unless included at relatively low levels or in a protected form, lipid supplements may adversely affect fibre degradation in the rumen. The current data are derived from a study conducted to evaluate the potential of an in vitro model to assess the effects of oil supplements on forage organic matter degradation (iOMD).

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