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Mol. Cells 2006; 21(1): 29-33

Published online January 1, 1970

© The Korean Society for Molecular and Cellular Biology

Establishment and Characterization of Three Immortal Bovine Muscular Epithelial Cell Lines

Xun Jin, Joong-Seob Lee, Sungwook Kwak, Soo-Yeon Lee, Ji-Eun Jung, Tae-Kyung Kim, Chenxiong Xu, Zhongshan Hong, Zhehu Li, Sun-Myung Kim, Xumin Pian, Dong-Hee Lee, Jong-Taek Yoon, Seungkwon You, Yun-Jaie Choi, Hyunggee Kim

Abstract

We have established three immortal bovine muscular epithelial (BME) cell lines, one spontaneously immortalized (BMES), the second SV40LT-mediated (BMEV) and the third hTERT-mediated (BMET). The morphology of the three immortal cell lines was similar to that of early passage primary BME cells. Each of the immortal cell lines made cytokeratin, a typical epithelial marker. BMET grew faster than the other immortal lines and the BME cells, in 10% FBS-DMEM medium, whereas neither the primary cells nor the three immortal cell lines grew in 0.5% FBS-DMEM. The primary BME cells and the immortal cell lines, with the exception of BMES, made increasing amounts of p53 protein when treated with doxorubicin, a DNA damaging agent. On the other hand, almost half of the cells in populations of the three immortal cell lines may lack p16INK4a regulatory function, compared to primary BME cells that were growth arrested by enforced expression of p16INK4a. In soft-agar assays, the primary cells and immortal cell lines proved to be less transformed in phenotype than HeLa cells. The three immortal epithelial-type cell lines reported here are the first cell lines established from muscle tissue of bovine or other species.

Keywords SV40LT; Telomerase, Immortalization; Muscle, Epithelial Cel

Article

Research Article

Mol. Cells 2006; 21(1): 29-33

Published online February 28, 2006

Copyright © The Korean Society for Molecular and Cellular Biology.

Establishment and Characterization of Three Immortal Bovine Muscular Epithelial Cell Lines

Xun Jin, Joong-Seob Lee, Sungwook Kwak, Soo-Yeon Lee, Ji-Eun Jung, Tae-Kyung Kim, Chenxiong Xu, Zhongshan Hong, Zhehu Li, Sun-Myung Kim, Xumin Pian, Dong-Hee Lee, Jong-Taek Yoon, Seungkwon You, Yun-Jaie Choi, Hyunggee Kim

Abstract

We have established three immortal bovine muscular epithelial (BME) cell lines, one spontaneously immortalized (BMES), the second SV40LT-mediated (BMEV) and the third hTERT-mediated (BMET). The morphology of the three immortal cell lines was similar to that of early passage primary BME cells. Each of the immortal cell lines made cytokeratin, a typical epithelial marker. BMET grew faster than the other immortal lines and the BME cells, in 10% FBS-DMEM medium, whereas neither the primary cells nor the three immortal cell lines grew in 0.5% FBS-DMEM. The primary BME cells and the immortal cell lines, with the exception of BMES, made increasing amounts of p53 protein when treated with doxorubicin, a DNA damaging agent. On the other hand, almost half of the cells in populations of the three immortal cell lines may lack p16INK4a regulatory function, compared to primary BME cells that were growth arrested by enforced expression of p16INK4a. In soft-agar assays, the primary cells and immortal cell lines proved to be less transformed in phenotype than HeLa cells. The three immortal epithelial-type cell lines reported here are the first cell lines established from muscle tissue of bovine or other species.

Keywords: SV40LT, Telomerase, Immortalization, Muscle, Epithelial Cel

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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