Thyrocytes, but not C cells, actively undergo growth and folliculogenesis at the periphery of thyroid tissue fragments in three-dimensional collagen gel culture

2003 ◽  
Vol 312 (3) ◽  
pp. 281-289 ◽  
Author(s):  
Shuji Toda ◽  
Shigehisa Aoki ◽  
Koichi Suzuki ◽  
Eisuke Koike ◽  
Akifumi Ootani ◽  
...  
2012 ◽  
Vol 21 (9) ◽  
pp. 2021-2032 ◽  
Author(s):  
Silvia Claros ◽  
Noela Rodríguez-Losada ◽  
Encarnación Cruz ◽  
Enrique Guerado ◽  
José Becerra ◽  
...  

1990 ◽  
Vol 226 (1) ◽  
pp. 91-107 ◽  
Author(s):  
Roger R. Markwald ◽  
David L. Bolender ◽  
Edward L. Krug ◽  
Ross Lepera

1997 ◽  
Vol 179 (2) ◽  
pp. 127-136 ◽  
Author(s):  
Masumi Akita ◽  
Eiko Murata ◽  
Hans-Joachim Merker ◽  
Katsuji Kaneko

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Shuji Toda ◽  
Shigehisa Aoki ◽  
Kazuyoshi Uchihashi ◽  
Aki Matsunobu ◽  
Mihoko Yamamoto ◽  
...  

The thyroid is composed of thyroid follicles supported by extracellular matrix, capillary network, and stromal cell types such as fibroblasts. The follicles consist of thyrocytes and C cells. In this microenvironment, thyrocytes are highly integrated in their specific structural and functional polarization, but monolayer and floating cultures cannot allow thyrocytes to organize the follicles with such polarity. In contrast, three-dimensional (3-D) collagen gel culture enables thyrocytes to form 3-D follicles with normal polarity. However, these systems never reconstruct the follicles consisting of both thyrocytes and C cells. Thyroid tissue-organotypic culture retains 3-D follicles with both thyrocytes and C cells. To create more appropriate experimental models, we here characterize four culture systems above and then introduce the models for studying thyroid biology and disorders. Finally, we propose a new approach to the cell type-specific culture systems on the basis of in vivo microenvironments of various cell types.


2002 ◽  
Vol 79 (4) ◽  
pp. 101-106 ◽  
Author(s):  
Keiko FUJITA ◽  
Yoshiko ASAMI ◽  
Eiko MURATA ◽  
Masumi AKITA ◽  
Katsuji KANEKO

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Masumi Akita ◽  
Kayoko Tanaka ◽  
Sachiko Matsumoto ◽  
Kumiko Komatsu ◽  
Keiko Fujita

We detected the hematopoietic stem and progenitor cell marker CD133 using immunogold labeling during angiogenesis in a three-dimensional collagen gel culture. CD133-positive cells were present in capillary tubes newly formed from aortic explants in vitro. The CD133-positive cell population had the capacity to form capillary tubes. Lovastatin strongly inhibited cell migration from aortic explants and caused the degradation of the capillary tubes. The present study provides insight into the function of CD133 during angiogenesis as well as an explanation for the antiangiogenic effect of statins.


Sign in / Sign up

Export Citation Format

Share Document