Subcellular redistribution and mitotic inheritance of transition metals in proliferating mouse fibroblast cells

42Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.

Abstract

Synchrotron X-ray fluorescence microscopy of non-synchronized NIH 3T3 fibroblasts revealed an intriguing redistribution dynamics that defines the inheritance of trace metals during mitosis. At metaphase, the highest density areas of Zn and Cu are localized in two distinct regions adjacent to the metaphase plate. As the sister chromatids are pulled towards the spindle poles during anaphase, Zn and Cu gradually move to the center and partition into the daughter cells to yield a pair of twin pools during cytokinesis. Colocalization analyses demonstrated high spatial correlations between Zn, Cu, and S throughout all mitotic stages, while Fe showed consistently different topographies characterized by high-density spots distributed across the entire cell. Whereas the total amount of Cu remained similar compared to interphase cells, mitotic Zn levels increased almost 3-fold, suggesting a prominent physiological role that lies beyond the requirement of Zn as a cofactor in metalloproteins or messenger in signaling pathways. © 2013 The Royal Society of Chemistry.

Cite

CITATION STYLE

APA

McRae, R., Lai, B., & Fahrni, C. J. (2013). Subcellular redistribution and mitotic inheritance of transition metals in proliferating mouse fibroblast cells. Metallomics, 5(1), 52–61. https://doi.org/10.1039/c2mt20176c

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free