scholarly journals Establishment, Culture, and Characterization of Guinea Pig Fetal Fibroblast Cell

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Davood Mehrabani ◽  
Reza Mahboobi ◽  
Mehdi Dianatpour ◽  
Shahrokh Zare ◽  
Amin Tamadon ◽  
...  

Establishment of Guinea pig fetal fibroblast cells and their biological evaluation before and after cryopreservation were the main purposes of this study. After determination of the proper age of pregnancy by ultrasonography, 30 days old fetuses of Guinea pigs were recovered. Their skins were cut into small pieces (1 mm2) and were cultured. When reaching 80–90% confluence, the cells were passaged. Cells of the second and eighth passages were cultured in 24-well plates (4×104cells/well) for 6 days and three wells per day were counted. The average cell counts at each time point were then plotted against time and the population doubling time (PDT) was determined. Then, vials of cells (2×106cells/mL) were cryopreserved for 1 month and after thawing, the cell viability was evaluated. The PDT of the second passage was about 23 h and for the eighth passage was about 30 h. The viability of the cultures was 95% in the second passage and 74.5% in the eighth passage. It was shown that the Guinea pig fetal fibroblast cell culture can be established using the adherent culture method while, after freezing, the viability indices of these cells were favorable.

2003 ◽  
Vol 36 (11) ◽  
pp. 1485-1489 ◽  
Author(s):  
M.R.B. Mello ◽  
H.V.A. Caetano ◽  
M.G. Marques ◽  
M.S. Padilha ◽  
J.F. Garcia ◽  
...  

2020 ◽  
Author(s):  
Tao Wang ◽  
Zelong Li ◽  
Jinpu Wei ◽  
Dongmin Zheng ◽  
Chen Wang ◽  
...  

AbstractThe population decline in the common hippopotamus (Hippopotamus amphibius) has necessitated the preservation of their genetic resources for species conservation and research. Of all actions, cryopreservation of fibroblast cell cultures derived from animal biopsy is considered a simple but efficient means. Nevertheless, preserving viable cell cultures of the common hippopotamus has not been achieved to our knowledge. To this end, we detailed a method to establish fibroblast cell cultures from a female common hippopotamus fetus in this study. By combining the classic tissue explant direct culture and enzymatic digestion methods, we isolated a great number of cells with typical fibroblastic morphology and high viability. Characterization of the fibroblast cultures was carried out using different techniques. In short, neither bacteria/fungi nor mycoplasma was detectable in the cell cultures throughout the study. The population doubling time was 23.9 h according to the growth curve. Karyotyping based on Giemsa staining showed that cultured cells were diploid with 36 chromosomes in all, one pair of which was sex chromosomes. Mitochondrial cytochrome C oxidase subunit I gene sequence of the cultured cells was 99.26% identical with the Hippopotamus amphibius complete mitochondrial DNA sequence registered in GenBank, confirming the cells were derived from a common hippopotamus. Flow cytometry and immunofluorescence staining results revealed that the detected cells were positive for fibroblast markers, S100A4 and Vimentin. In conclusion, we isolated and characterized a new fibroblast cell culture from a common hippopotamus skin sample and the cryopreserved cells could be useful genetic materials for the future research.


1970 ◽  
Vol 4 (6) ◽  
pp. 511-511
Author(s):  
Antoinette Condon ◽  
Frank A Oski ◽  
Salvatore DiMauro ◽  
William J Mellman

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