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p19ARF determines the balance between normal cell proliferation rate and apoptosis during mammary gland development (CROSBI ID 195247)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Yi, Y. ; Shepard, A. ; Kittrell, F. ; Mulac-Jeričević, Biserka ; Medina, D. ; Said, T.K. p19ARF determines the balance between normal cell proliferation rate and apoptosis during mammary gland development // Molecular biology of the cell, 15 (2004), 5; 2302-2311. doi: 10.1091/mbc.E03-11-0785

Podaci o odgovornosti

Yi, Y. ; Shepard, A. ; Kittrell, F. ; Mulac-Jeričević, Biserka ; Medina, D. ; Said, T.K.

engleski

p19ARF determines the balance between normal cell proliferation rate and apoptosis during mammary gland development

This study demonstrated, for the first time, the following events related to p19(ARF) involvement in mammary gland development: 1) Progesterone appears to regulate p19(ARF) in normal mammary gland during pregnancy. 2) p19(ARF) expression levels increased sixfold during pregnancy, and the protein level plateaus during lactation. 3) During involution, p19(ARF) protein level remained at high levels at 2 and 8 days of involution and then, declined sharply at day 15. Absence of p19(ARF) in mammary epithelial cells leads to two major changes, 1) a delay in the early phase of involution concomitant with downregulation of p21(Cip1) and decrease in apoptosis, and 2) p19(ARF) null cells are immortal in vivo measured by serial transplantion, which is partly attributed to complete absence of p21(Cip1) compared with WT cells. Although, p19(ARF) is dispensable in mammary alveologenesis, as evidenced by normal differentiation in the mammary gland of pregnant p19(ARF) null mice, the upregulation of p19(ARF) by progesterone in the WT cells and the weakness of p21(Cip1) in mammary epithelial cells lacking p19(ARF) strongly suggest that the functional role(s) of p19(ARF) in mammary gland development is critical to sustain normal cell proliferation rate during pregnancy and normal apoptosis in involution possibly through the p53-dependent pathway.

tumor suppresor gene; p53; mice

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Podaci o izdanju

15 (5)

2004.

2302-2311

objavljeno

1059-1524

10.1091/mbc.E03-11-0785

Povezanost rada

Temeljne medicinske znanosti

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