3D-Human Small Intestinal Tissue Model System to Screen Drug Induced Gastrointestinal Toxicity and Wound Healing

Author(s):  
Seyoum Ayehunie
2014 ◽  
Vol 229 ◽  
pp. S144 ◽  
Author(s):  
Seyoum Ayehunie ◽  
Zacharey Stevens ◽  
Tim Landry ◽  
Mitchell Klausner ◽  
Patrik Hayden ◽  
...  

2017 ◽  
Vol 280 ◽  
pp. S271 ◽  
Author(s):  
Seyoum Ayehunie ◽  
Zachary Stevens ◽  
Timothy Landry ◽  
Alex Armento ◽  
Mitchell Klausner ◽  
...  

2013 ◽  
Vol 221 ◽  
pp. S88 ◽  
Author(s):  
Seyoum Ayehunie ◽  
Zachary Stevens ◽  
Timothy Landry ◽  
Alexander Armento ◽  
Mitchell Klausner ◽  
...  

PLoS ONE ◽  
2019 ◽  
Vol 14 (2) ◽  
pp. e0211436 ◽  
Author(s):  
Sunao Shimada ◽  
Tetsuya Tanigawa ◽  
Toshio Watanabe ◽  
Akinobu Nakata ◽  
Naoki Sugimura ◽  
...  

2014 ◽  
Vol 83 (1) ◽  
pp. 28-38 ◽  
Author(s):  
Teresa M. DesRochers ◽  
Erica Palma Kimmerling ◽  
Dakshina M. Jandhyala ◽  
Wassim El-Jouni ◽  
Jing Zhou ◽  
...  

Shiga toxins (Stx) are a family of cytotoxic proteins that can cause hemolytic-uremic syndrome (HUS), a thrombotic microangiopathy, following infections by Shiga toxin-producingEscherichia coli(STEC). Renal failure is a key feature of HUS and a major cause of childhood renal failure worldwide. There are currently no specific therapies for STEC-associated HUS, and the mechanism of Stx-induced renal injury is not well understood primarily due to a lack of fully representative animal models and an inability to monitor disease progression on a molecular or cellular level in humans at early stages. Three-dimensional (3D) tissue models have been shown to be morein vivo-like in their phenotype and physiology than 2D cultures for numerous disease models, including cancer and polycystic kidney disease. It is unknown whether exposure of a 3D renal tissue model to Stx will yield a morein vivo-like response than 2D cell culture. In this study, we characterized Stx2-mediated cytotoxicity in a bioengineered 3D human renal tissue model previously shown to be a predictor of drug-induced nephrotoxicity and compared its response to Stx2 exposure in 2D cell culture. Our results demonstrate that although many mechanistic aspects of cytotoxicity were similar between 3D and 2D, treatment of the 3D tissues with Stx resulted in an elevated secretion of the kidney injury marker 1 (Kim-1) and the cytokine interleukin-8 compared to the 2D cell cultures. This study represents the first application of 3D tissues for the study of Stx-mediated kidney injury.


Author(s):  
Veronica G. Martinez Acosta ◽  
Fausto Arellano-Carbajal ◽  
Kathy Gillen ◽  
Kay A. Tweeten ◽  
Eduardo E. Zattara

The mechanisms supporting regeneration and successful recovery of function have fascinated scientists and the general public for quite some time, with the earliest description of regeneration occurring in the 8th century BC through the Greek mythological story of Prometheus. While most animals demonstrate the capacity for wound-healing, the ability to initiate a developmental process that leads to a partial or complete replacement of a lost structure varies widely among animal taxa. Variation also occurs within single species based on the nature and location of the wound and the developmental stage or age of the individual. Comparative studies of cellular and molecular changes that occur both during, and following, wound healing may point to conserved genomic pathways among animals of different regenerative capacity. Such insights could revolutionize studies within the field of regenerative medicine. In this review, we focus on several closely related species of Lumbriculus (Clitellata: Lumbriculidae), as we present a case for revisiting the use of an annelid model system for the study of regeneration. We hope that this review will provide a primer to Lumbriculus biology not only for regeneration researchers but also for STEM teachers and their students.


2010 ◽  
Vol 18 (3) ◽  
pp. 291-301 ◽  
Author(s):  
Neeltje A. Coolen ◽  
Kelly C. W. M. Schouten ◽  
Bouke K. H. L. Boekema ◽  
Esther Middelkoop ◽  
Magda M. W. Ulrich

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