Anas Mohamed-Kheir Idris, Hammer Mary-Anne, Lever Michael, Stanton Jo-Ann L, Baltz Jay M
Hormones, Growth and Development Program, Ottawa Health Research Institute, Ottawa, Ontario, Canada.
J Cell Physiol. 2007 Jan;210(1):266-77. doi: 10.1002/jcp.20872.
Betaine and proline protect preimplantation mouse embryos against increased osmolarity and decreased cell volume, implying that they may function as organic osmolytes. However, the transport system(s) that mediates their accumulation in fertilized eggs and early embryos was unknown, and previously identified mammalian organic osmolyte transporters could not account for their transport. Here, we report that there is a single saturable transport component shared by betaine and proline in 1-cell mouse embryos. A series of inhibitors had nearly identical effects on both betaine and proline transport by this system. In addition, K(i) values for reciprocal inhibition of betaine and proline transport were approximately 100-300 microM, similar to K(m) values ( approximately 200-300 microM) for their transport, and both had similar maximal transport rates (V(max)). The K(i) values for inhibition of betaine and proline transport by dimethylglycine were similar ( approximately 2 mM), further supporting transport of both substrates by a single transport system. Finally, betaine and proline transport each required Na(+)- and Cl(-). These data were consistent with a single, Na(+)- and Cl(-)-requiring, betaine/proline transport system in 1-cell mouse embryos. While betaine was only transported by a single saturable system, we found an additional, less conspicuous proline transport route that was betaine-insensitive, Na(+)-sensitive, and inhibited by alanine, leucine, cysteine, and methionine. Furthermore, we showed that betaine, like proline, is present in the mouse oviduct and thus could serve as a physiological substrate. Finally, accumulation of both betaine and proline increased with increasing osmolarity, consistent with a possible role as organic osmolytes in early embryos.
甜菜碱和脯氨酸可保护植入前的小鼠胚胎免受渗透压升高和细胞体积减小的影响,这意味着它们可能作为有机渗透溶质发挥作用。然而,介导它们在受精卵和早期胚胎中积累的转运系统尚不清楚,而且先前鉴定出的哺乳动物有机渗透溶质转运体无法解释它们的转运过程。在此,我们报告在单细胞小鼠胚胎中,甜菜碱和脯氨酸共享单一的可饱和转运成分。一系列抑制剂对该系统介导的甜菜碱和脯氨酸转运具有几乎相同的作用。此外,甜菜碱和脯氨酸转运相互抑制的抑制常数(Ki)值约为100 - 300微摩尔,与其转运的米氏常数(Km)值(约200 - 300微摩尔)相似,且二者具有相似的最大转运速率(Vmax)。二甲基甘氨酸对甜菜碱和脯氨酸转运的抑制常数(Ki)值相似(约2毫摩尔),进一步支持两种底物通过单一转运系统进行转运。最后,甜菜碱和脯氨酸的转运均需要钠离子(Na+)和氯离子(Cl-)。这些数据与单细胞小鼠胚胎中存在单一的、需要钠离子和氯离子的甜菜碱/脯氨酸转运系统一致。虽然甜菜碱仅通过单一的可饱和系统进行转运,但我们发现了另一条不太明显的脯氨酸转运途径,该途径对甜菜碱不敏感、对钠离子敏感,并受到丙氨酸、亮氨酸、半胱氨酸和蛋氨酸的抑制。此外,我们表明甜菜碱与脯氨酸一样,存在于小鼠输卵管中,因此可作为一种生理底物。最后,随着渗透压的升高,甜菜碱和脯氨酸的积累均增加,这与它们在早期胚胎中作为有机渗透溶质的可能作用一致。