scholarly journals Establishment of a three‐dimensional primary cell culture model of equine papillomavirus type 2 infection

2021 ◽  
Vol 53 (S56) ◽  
pp. 34-35
Keyword(s):  
Cell Culture ◽  
Primary Cell Culture ◽  
Three Dimensional ◽  
Primary Cell ◽  
Cell Culture Model ◽  
Culture Model

scholarly journals Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model

2017 ◽  
Vol 58 (2) ◽  
pp. 708 ◽  
Author(s):  
Matthew G. Pilgrim ◽  
Imre Lengyel ◽  
Antonio Lanzirotti ◽  
Matt Newville ◽  
Sarah Fearn ◽  
...  
Keyword(s):  
Cell Culture ◽  
Primary Cell Culture ◽  
Primary Cell ◽  
Cell Culture Model ◽  
Pigment Epithelial ◽  
Culture Model

A primary cell culture model for defective cardiac myofibrillogenesis in mexican axolotl embryos

1997 ◽  
Vol 33 (9) ◽  
pp. 677-680
Author(s):  
Robert W. Zajdel ◽  
Yongze Zhu ◽  
Margaret E. Fransen ◽  
Larry F. Lemanski
Keyword(s):  
Cell Culture ◽  
Primary Cell Culture ◽  
Primary Cell ◽  
Cell Culture Model ◽  
Mexican Axolotl ◽  
Culture Model

Lactoferrin Expression by Bovine Ocular Surface Epithelia: A Primary Cell Culture Model to Study Lactoferrin Gene Promoter Activity

2005 ◽  
Vol 37 (5) ◽  
pp. 270-278 ◽  
Author(s):  
Maria Grazia Santagati ◽  
Simona La Terra Mulè ◽  
Carla Amico ◽  
Matteo Pistone ◽  
Dario Rusciano ◽  
...  
Keyword(s):  
Cell Culture ◽  
Ocular Surface ◽  
Promoter Activity ◽  
Primary Cell Culture ◽  
Gene Promoter ◽  
Primary Cell ◽  
Cell Culture Model ◽  
Culture Model ◽  
Lactoferrin Gene

S1792 Effects of Ethanol and Acetaldehyde on Epithelial Integrity in a Three Dimensional (3D) Epithelial Cell Culture Model

2010 ◽  
Vol 138 (5) ◽  
pp. S-275
Author(s):  
Elhaseen Elamin ◽  
Daisy Jonkers ◽  
Freddy Troost ◽  
Kati Juuti-Uusitalo ◽  
Sven C. van IJzendoorn ◽  
...  
Keyword(s):  
Cell Culture ◽  
Epithelial Cell ◽  
Three Dimensional ◽  
Cell Culture Model ◽  
Epithelial Cell Culture ◽  
Epithelial Integrity ◽  
Culture Model

scholarly journals Effects of Ethanol and Acetaldehyde on Tight Junction Integrity: In Vitro Study in a Three Dimensional Intestinal Epithelial Cell Culture Model

PLoS ONE ◽  
2012 ◽  
Vol 7 (4) ◽  
pp. e35008 ◽  
Author(s):  
Elhaseen Elamin ◽  
Daisy Jonkers ◽  
Kati Juuti-Uusitalo ◽  
Sven van IJzendoorn ◽  
Freddy Troost ◽  
...  
Keyword(s):  
Cell Culture ◽  
Epithelial Cell ◽  
Intestinal Epithelial Cell ◽  
Three Dimensional ◽  
In Vitro Study ◽  
Intestinal Epithelial ◽  
Cell Culture Model ◽  
Epithelial Cell Culture ◽  
Culture Model

A magnetic three‐dimensional levitated primary cell culture system for the development of secretory salivary gland‐like organoids

2019 ◽  
Vol 13 (3) ◽  
pp. 495-508 ◽  
Author(s):  
Joao N. Ferreira ◽  
Riasat Hasan ◽  
Ganokon Urkasemsin ◽  
Kiaw K. Ng ◽  
Christabella Adine ◽  
...  
Keyword(s):  
Cell Culture ◽  
Salivary Gland ◽  
Culture System ◽  
Primary Cell Culture ◽  
Three Dimensional ◽  
Primary Cell ◽  
Cell Culture System

scholarly journals The Late-Stage Protective Effect of Mito-TEMPO against Acetaminophen-Induced Hepatotoxicity in Mouse and Three-Dimensional Cell Culture Models

Antioxidants ◽  
2020 ◽  
Vol 9 (10) ◽  
pp. 965
Author(s):  
Mohammad Abdullah-Al-Shoeb ◽  
Kenta Sasaki ◽  
Saori Kikutani ◽  
Nanami Namba ◽  
Keiichi Ueno ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Cell Culture ◽  
Liver Injury ◽  
Protective Effect ◽  
Acute Liver Injury ◽  
Three Dimensional ◽  
3D Cell Culture ◽  
Cell Culture Model ◽  
Culture Model ◽  
Apap Hepatotoxicity

An overdose of acetaminophen (APAP), the most common cause of acute liver injury, induces oxidative stress that subsequently causes mitochondrial impairment and hepatic necroptosis. N-acetyl-L-cysteine (NAC), the only recognized drug against APAP hepatotoxicity, is less effective the later it is administered. This study evaluated the protective effect of mitochondria-specific Mito-TEMPO (Mito-T) on APAP-induced acute liver injury in C57BL/6J male mice, and a three dimensional (3D)-cell culture model containing the human hepatoblastoma cell line HepG2. The administration of Mito-T (20 mg/kg, i.p.) 1 h after APAP (400 mg/kg, i.p.) injection markedly attenuated the APAP-induced elevated serum transaminase activity and hepatic necrosis. However, Mito-T treatment did not affect key factors in the development of APAP liver injury including the activation of c-jun N-terminal kinases (JNK), and expression of the transcription factor C/EBP homologous protein (CHOP) in the liver. However, Mito-T significantly reduced the APAP-induced increase in the hepatic oxidative stress marker, nitrotyrosine, and DNA fragmentation. Mito-T markedly attenuated cytotoxicity induced by APAP in the HepG2 3D-cell culture model. Moreover, liver regeneration after APAP hepatotoxicity was not affected by Mito-T, demonstrated by no changes in proliferating cell nuclear antigen formation. Therefore, Mito-T was hepatoprotective at the late-stage of APAP overdose in mice.

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