Amino acid transport mechanisms in mouse oocytes during growth and meiotic maturation

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Abstract

Amino acids are transported into cells by a number of different transport systems, each with their own specific range of substrates. The amino acid transport systems active in preimplantation embryos and the amino acids required by embryos for optimal development have been extensively investigated. Much less is known about amino acid transport systems active in growing and meiotically maturing oocytes or about developmental changes in their activity. As a first step in determining the array of amino acid transporters active in oocytes, the transport characteristics of nine amino acids were measured in small, medium, and large growing oocytes; in fully grown germinal vesicle (GV)-stage oocytes; in metaphase I oocytes; and in metaphase II eggs. Whether each of 11 classically defined amino acid transport systems was likely active in oocytes at each stage was determined using assays based on measuring the transport of radiolabeled amino acids into oocytes and the effect of a limited set of potential competitive inhibitors. Six amino acid transport systems were found to be active during oocyte growth or maturation. L, b0,+, and ASC/asc were active throughout oocyte growth and maturation, increasing during growth. In contrast, GLY, beta, and xc- had little or no activity during growth but became activated during meiotic maturation. Surprisingly, the presence of follicular cells surrounding medium growing oocytes or cumulus cells surrounding GV oocytes did not confer amino acid transport by additional transport systems not present in the oocyte. In some cases, however, follicular cells coupled to the oocyte enhanced uptake of amino acids by the same systems present in the oocyte. © 2009 by the Society for the Study of Reproduction, Inc.

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Pelland, A. M. D., Corbett, H. E., & Baltz, J. M. (2009). Amino acid transport mechanisms in mouse oocytes during growth and meiotic maturation. Biology of Reproduction, 81(6), 1041–1054. https://doi.org/10.1095/biolreprod.109.079046

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