Mammary alveolar cell as in vitro evaluation system for casein gene expression involved in glucose level

• Published in: Animal bioscience Vol. 30; no. 6; pp. 878 - 885
• Main Authors: Heo, Young Tae, Ha, Woo Tae, Lee, Ran, Lee, Won-Young, Jeong, Ha Yeon, Hwang, Kyu Chan, Song, Hyuk
• Format: Journal Article
• Language: English
• Published: Korea (South) Asian - Australasian Association of Animal Production Societies 01.06.2017; Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST); 아세아·태평양축산학회
• Subjects: Casein; Cell metabolism; Genetic aspects; Glucose metabolism; In vitro tests; Lactation; Mammary glands; Methods; Physiological aspects; 축산학; South Korea; Insulin-like Growth Factor-1 (IGF-1); Glucose; Casein; Oxytocin; Mammary alveolar (MAC-T) Cell
• ISSN: 1011-2367; 2765-0189; 1976-5517; 2765-0235
• DOI: 10.5713/ajas.16.0515

Glucose is an essential fuel in the energy metabolism and synthesis pathways of all mammalian cells. In lactating animals, glucose is the major precursor for lactose and is a substrate for the synthesis of milk proteins and fat in mammary secretory (alveolar) epithelial cells. However, clear utilization of glucose in mammary cells during lactogenesis is still unknown, due to the lack of analyzing models. Therefore, the objective of this study was to test the reliability of the mammary alveolar (MAC-T) cell as an study model for glucose metabolism and lactating system. Undifferentiated MAC-T cells were cultured in three types of Dulbecco's modified Eagle's medium with varying levels of glucose (no-glucose: 0 g/L, low-glucose: 1 g/L, and high-glucose: 4.5 g/L) for 8 d, after which differentiation to casein secretion was induced. Cell proliferation and expression levels of apoptotic genes, Insulin like growth factor-1 (IGF1) receptor, oxytocin receptor, αS1, αS2, and β casein genes were analyzed at 1, 2, 4, and 8 d after differentiation. The proliferation of MAC-T cells with high-glucose treatment was seen to be significantly higher. Expression of apoptotic genes was not affected in any group. However, expression levels of the mammary development related gene (IGF1 receptor) and lactation related gene (oxytocin receptor) were significantly higher in the low-glucose group. Expressions of αS1-casein, αS2-casein, and β-casein were also higher in the low-glucose treated group as compared to that in the no-glucose and high-glucose groups. The results demonstrated that although a high-glucose environment increases cell proliferation in MAC-T cells, a low-glucose treatment to MAC-T cells induces higher expression of casein genes. Our results suggest that the MAC-T cells may be used as an model to analyze mammary cell development and lactation connected with precise biological effects.