scholarly journals Development of Three-Dimensional Micro Vibration Stage and Its Application to Control Device for Cell Culture

2008 ◽  
Vol 3 (1) ◽  
pp. 38-49 ◽  
Author(s):  
Ken-ichi KONNO ◽  
Tadashi KOSAWADA ◽  
Hiroshi YAMAZAKI ◽  
Yasukazu HOZUMI ◽  
Kaoru GOTO
Author(s):  
Ken-ichi Konno ◽  
Tadashi Kosawada ◽  
Ryota Sato ◽  
Zhonggang Feng ◽  
Yasukazu Hozumi ◽  
...  

2008 ◽  
Vol 2008 (0) ◽  
pp. _341-1_-_341-6_
Author(s):  
Ryota SATO ◽  
Ken-ichi KONNO ◽  
Tadashi KOSAWADA ◽  
Yasukazu HOZUMI ◽  
Kaoru GOTO

2012 ◽  
Vol 2012.48 (0) ◽  
pp. 56-57
Author(s):  
Takanari GOTO ◽  
Ken-ichi KONNO ◽  
Tadashi KOSAWADA ◽  
Zhonggang FENG ◽  
Yasukazu HOZUMI ◽  
...  

2009 ◽  
Vol 2009 (0) ◽  
pp. _238-1_-_238-6_
Author(s):  
Ryota SATO ◽  
Ken-ichi KONNO ◽  
Tadashi KOSAWADA ◽  
Kaoru GOTO

2010 ◽  
Vol 2010 (0) ◽  
pp. _433-1_-_433-6_
Author(s):  
Toru ICHITA ◽  
Ken-ichi KONNO ◽  
Yasushi KANEYAMA ◽  
Ryota SATO ◽  
Tadashi KOSAWADA ◽  
...  

2021 ◽  
Vol 22 (5) ◽  
pp. 2491
Author(s):  
Yujin Park ◽  
Kang Moo Huh ◽  
Sun-Woong Kang

The process of evaluating the efficacy and toxicity of drugs is important in the production of new drugs to treat diseases. Testing in humans is the most accurate method, but there are technical and ethical limitations. To overcome these limitations, various models have been developed in which responses to various external stimuli can be observed to help guide future trials. In particular, three-dimensional (3D) cell culture has a great advantage in simulating the physical and biological functions of tissues in the human body. This article reviews the biomaterials currently used to improve cellular functions in 3D culture and the contributions of 3D culture to cancer research, stem cell culture and drug and toxicity screening.


2021 ◽  
Vol 183 ◽  
pp. 113215
Author(s):  
Patrycja Sokolowska ◽  
Kamil Zukowski ◽  
Justyna Janikiewicz ◽  
Elzbieta Jastrzebska ◽  
Agnieszka Dobrzyn ◽  
...  

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Laurence Finot ◽  
Eric Chanat ◽  
Frederic Dessauge

AbstractIn vivo study of tissue or organ biology in mammals is very complex and progress is slowed by poor accessibility of samples and ethical concerns. Fortunately, however, advances in stem cell identification and culture have made it possible to derive in vitro 3D “tissues” called organoids, these three-dimensional structures partly or fully mimicking the in vivo functioning of organs. The mammary gland produces milk, the source of nutrition for newborn mammals. Milk is synthesized and secreted by the differentiated polarized mammary epithelial cells of the gland. Reconstructing in vitro a mammary-like structure mimicking the functional tissue represents a major challenge in mammary gland biology, especially for farm animals for which specific agronomic questions arise. This would greatly facilitate the study of mammary gland development, milk secretion processes and pathological effects of viral or bacterial infections at the cellular level, all with the objective of improving milk production at the animal level. With this aim, various 3D cell culture models have been developed such as mammospheres and, more recently, efforts to develop organoids in vitro have been considerable. Researchers are now starting to draw inspiration from other fields, such as bioengineering, to generate organoids that would be more physiologically relevant. In this chapter, we will discuss 3D cell culture systems as organoids and their relevance for agronomic research.


Author(s):  
Terry Riss ◽  
O. Joseph Trask

AbstractAlong with the increased use of more physiologically relevant three-dimensional cell culture models comes the responsibility of researchers to validate new assay methods that measure events in structures that are physically larger and more complex compared to monolayers of cells. It should not be assumed that assays designed using monolayers of cells will work for cells cultured as larger three-dimensional masses. The size and barriers for penetration of molecules through the layers of cells result in a different microenvironment for the cells in the outer layer compared to the center of three-dimensional structures. Diffusion rates for nutrients and oxygen may limit metabolic activity which is often measured as a marker for cell viability. For assays that lyse cells, the penetration of reagents to achieve uniform cell lysis must be considered. For live cell fluorescent imaging assays, the diffusion of fluorescent probes and penetration of photons of light for probe excitation and fluorescent emission must be considered. This review will provide an overview of factors to consider when implementing assays to interrogate three dimensional cell culture models.


Sign in / Sign up

Export Citation Format

Share Document