Innovation in culture systems to study muscle complexity

2021 ◽  
pp. 112966
Author(s):  
Louise A. Moyle ◽  
Sadegh Davoudi ◽  
Penney M. Gilbert
Keyword(s):  
Author(s):  
A. R. Crooker ◽  
M. C. Myers ◽  
T. L. Beard ◽  
E. S. Graham

Cell culture systems have become increasingly popular as a means of screening toxic agents and studying toxic mechanisms of drugs and other chemicals at the cellular and subcellular levels. These in vitro tests can be conducted rapidly in a broad range of relevant mammalian culture systems; a variety of biological and biochemical cytotoxicity endpoints can be examined. The following study utilized human keratinocytes to evaluate the relative cytotoxicities of nitrofurazone (NF) and silver sulfadiazine (SS), the active ingredients of FURACIN(R) Topical Cream and SILVADENE(R) Cream, respectively. These compounds are anti-infectives used in the treatment of burn patients. Cell ultrastructure and elemental composition were utilized as cytotoxicity endpoints.Normal Human Epidermal Keratinocytes (HK) were prepared from the EpiPackTM culture system (Clonetics Corporation, Boulder, CO). For scanning electron microscopy (SEM) and transmission electron microscopy (TEM), cells were seeded on sterile 35 mm Falcon plastic dishes; for elemental microanalysis, cells were plated on polished pyrolytic carbon discs (E. Fullam, Latham, NY) placed in the culture dishes.


2018 ◽  
Author(s):  
Fantuzzi Federica ◽  
Toivonen Sanna ◽  
Schiavo Andrea Alex ◽  
Pachera Nathalie ◽  
Rajaei Bahareh ◽  
...  

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 459d-459
Author(s):  
Fumiomi Takeda ◽  
Paul R. Adler ◽  
D. Michael Glenn

Strawberry plants (cvs. Camarosa, Chandler, Sweet Charlie, Primetime, Jewel, and Tribute) were grown in soilless culture systems in a greenhouse from October to May. Fresh-dug and runner-tip Aplug® plants were transplanted into two systems: vertically stacked pots (24 plants/m2) containing perlite and horizontal nutrient film technique troughs (13 plants/m2). Plants were fertigated continuously with recirculating nutrient solution. In a 7-month production cycle, the plug plants bloomed earlier and produced more fruit during the first month of harvest (December) than the fresh-dug plants. Higher yields from plug plants were a result of more fruit numbers and not larger fruit size. Fruit production averaged 6.0 and 3.5 kg/m2 in the trough and pot systems, respectively. The vertical growing system allows greater plant densities, but light intensity reaching the plants in the lower sections of the tower can be less than 20% of levels measured at the top. Establishment costs of protected culture systems are higher, but production is earlier and labor costs are typically reduced. Greenhouse hydroponic culture systems could extend the winter strawberry production to more northern locations.


2020 ◽  
Vol 14 ◽  
Author(s):  
Shogo Ozawa ◽  
Toshitaka Miura ◽  
Jun Terashima ◽  
Wataru Habano ◽  
Seiichi Ishida

Background: In order to avoid drug-induced liver injury (DILI), in vitro assays, which enable the assessment of both metabolic activation and immune reaction processes that ultimately result in DILI, are needed. Objective: In this study, the recent progress in the application of in vitro assays using cell culture systems is reviewed for potential DILI-causing drugs/xenobiotics and a mechanistic study on DILI, as well as for the limitations of in vitro cell culture systems for DILI research. Methods: Information related to DILI was collected through a literature search of the PubMed database. Results: The initial biological event for the onset of DILI is the formation of cellular protein adducts after drugs have been metabolically activated by drug metabolizing enzymes. The damaged peptides derived from protein adducts lead to the activation of CD4+ helper T lymphocytes and recognition by CD8+ cytotoxic T lymphocytes, which destroy hepatocytes through immunological reactions. Because DILI is a major cause of drug attrition and drug withdrawal, numerous in vitro systems consisting of hepatocytes and immune/inflammatory cells, or spheroids of human primary hepatocytes containing non-parenchymal cells have been developed. These cellular-based systems have identified DILIinducing drugs with approximately 50% sensitivity and 90% specificity. Conclusion: Different co-culture systems consisting of human hepatocyte-derived cells and other immune/inflammatory cells have enabled the identification of DILI-causing drugs and of the actual mechanisms of action.


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