Mol. Cells 2003; 15(1): 10-19
Published online January 1, 1970
© The Korean Society for Molecular and Cellular Biology
Delayed death of serum-starved PC12 cells on a poly-L-lysine (PLL) matrix was observed, even in the presence of NGF. NGF blocked the apoptotic death of attached but not detached cells, which suggests that delayed death may be related to cell detachment from the PLL matrix. Iron selectively blocked this anoikis-like death by increasing cell attachment. Interestingly, the addition of > 10 mM FeCl2 to the culture medium generated gelatinous iron precipitates, and the removal of the precipitates abolished the iron effect. Attachment experiments using poly-HEMA supported the role of iron precipitates on cell-to-matrix adhesion. The expression of integrin b1, neither N-cadherin nor a/b-catenin, was also significantly increased by iron. In addition to its effect on cell viability, iron promoted the outgrowth of neurites. Our results collectively indicate that iron functions as a necessary co-element for NGF by enhancing cell attachment, survival, and neurite extension.
Keywords Neurite Outgrowth, NGF, PC12 Cells, Iron, Cell Attachment
Mol. Cells 2003; 15(1): 10-19
Published online February 28, 2003
Copyright © The Korean Society for Molecular and Cellular Biology.
Jin-hee Hong, Kyung-min Noh, Young-eun Yoo, So-young Choi, Sun-young Park, Yoon-hee Kim, Jun-mo Chung
Delayed death of serum-starved PC12 cells on a poly-L-lysine (PLL) matrix was observed, even in the presence of NGF. NGF blocked the apoptotic death of attached but not detached cells, which suggests that delayed death may be related to cell detachment from the PLL matrix. Iron selectively blocked this anoikis-like death by increasing cell attachment. Interestingly, the addition of > 10 mM FeCl2 to the culture medium generated gelatinous iron precipitates, and the removal of the precipitates abolished the iron effect. Attachment experiments using poly-HEMA supported the role of iron precipitates on cell-to-matrix adhesion. The expression of integrin b1, neither N-cadherin nor a/b-catenin, was also significantly increased by iron. In addition to its effect on cell viability, iron promoted the outgrowth of neurites. Our results collectively indicate that iron functions as a necessary co-element for NGF by enhancing cell attachment, survival, and neurite extension.
Keywords: Neurite Outgrowth, NGF, PC12 Cells, Iron, Cell Attachment
So Yun Park, Ji Yun Lee, Jun Young Choi, Mae Ja Park, Dong Sun Kim
Mol. Cells 2006; 21(2): 237-243 https://doi.org/10.14348/.2006.21.2.237Young-eun Yoo, Jin-hee Hong, Kyu Chung Hur, Eok-Soo Oh, Jun-mo Chung
Mol. Cells 2004; 17(2): 340-346 https://doi.org/10.14348/.2004.17.2.340Hyeongjin Cho, Dong Yoon Lee, Suja Shrestha, Yi Sup Shim, Ki Chul Kim, Mee-Kyung Kim, Keun-Hyeung Lee, Jonghwa Won, Jae-Seung Kang
Mol. Cells 2004; 18(1): 46-52 https://doi.org/10.14348/.2004.18.1.46