scholarly journals Evaluation of Absorbability of Macromolecular Substances in the Oral Mucosa and Skin using a Three-Dimensional Tissue Culture Model

2018 ◽  
Vol 10 (5) ◽  
Author(s):  
Mariko Takenokuchi ◽  
Keiichi Kadoyama ◽  
Daisuke Yoshida ◽  
Shigeki Takaki ◽  
Ryoma Yamamoto ◽  
...  
2014 ◽  
Vol 20 (1) ◽  
pp. 42-51 ◽  
Author(s):  
Lucia Speroni ◽  
Gregory S. Whitt ◽  
Joanna Xylas ◽  
Kyle P. Quinn ◽  
Adeline Jondeau-Cabaton ◽  
...  

2013 ◽  
Vol 9 (8) ◽  
pp. 7908-7916 ◽  
Author(s):  
Mark S.F. Clarke ◽  
Alamelu Sundaresan ◽  
Charles R. Vanderburg ◽  
Meredith G. Banigan ◽  
Neal R. Pellis

2003 ◽  
Vol 284 (5) ◽  
pp. H1771-H1777 ◽  
Author(s):  
Chee Ping Ng ◽  
Melody A. Swartz

Interstitial flow is an important component of the microcirculation and interstitial environment, yet its effects on cell organization and tissue architecture are poorly understood, in part due to the lack of in vitro models. To examine the effects of interstitial flow on cell morphology and matrix remodeling, we developed a tissue culture model that physically supports soft tissue cultures and allows microscopic visualization of cells within the three-dimensional matrix. In addition, pressure-flow relationships can be continuously monitored to evaluate the bulk hydraulic resistance as an indicator of changes in the overall matrix integrity. We observed that cells such as human dermal fibroblasts aligned perpendicular to the direction of interstitial flow. In contrast, fibroblasts in static three-dimensional controls remained randomly oriented, whereas cells subjected to fluid shear as a two-dimensional monolayer regressed. Also, the dynamic measurements of hydraulic conductivity suggest reorganization toward a steady state. These primary findings help establish the importance of interstitial flow on the biology of tissue organization and interstitial fluid balance.


Author(s):  
Parviz Ranjbarvan ◽  
Fatemeh Khazaei ◽  
Farzaneh Chobsaz ◽  
Mozafar Khazaei

Introduction: Raloxifene (Ral) is the oldest SERM (selective oestrogen receptor modulators) for treatment of breast cancer and osteoporosis. Its oestrogen-modulating effects have been shown in breast and uterus. Since there is little available data on direct Ral effect on the human endometrium, the aim of present study was to investigate the Ral effect on the growth and angiogenesis of the human endometrium of healthy and endometriosis subjects in an in vitro three-dimensional (3D) tissue culture model. Material and methods: Endometrial biopsies from healthy ( n = 9) and endometriosis ( n = 7) patients (endometriotic) were taken and were cut into 1 × 1 mm fragments and implanted between two layers of fibrin jell made by fibrinogen solution (3 mg/ml in medium 199+thrombin). Tissue cultures were performed in 24-wel culture plates. Each biopsy was divided into control wells which received M199 supplemented with FBS (5%) and experimental wells which received same media containing one of raloxifene doses (0.1, 1 and 10 μM). Endometrial tissues were photographed at the beginning and the end of the study period (21 days). Tissue growth and angiogenesis were determined by a scoring system. Results: In control (0), 0.1, 1 and 10 μM Ral, the growth score of normal human endometrial tissues were 1.99, 1.72, 1.53 and 1.12 ( p = 0.02) and angiogenesis percent were 29.6%, 31.28%, 33% and 11.5%. The Growth scores of the endometriotic endometrium were 1.92, 1.82, 1.92 and 1.1 ( p = 0.008) and angiogenesis percent were 36.6%, 16.6%, 44% and 12.5% respectively. Conclusion: Raloxifene showed a different dose dependent effect on endometrial and endometriotic tissue.


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