Burrows C, Blum J J
Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710.
J Protozool. 1991 Jan-Feb;38(1):47-52. doi: 10.1111/j.1550-7408.1991.tb04799.x.
Earlier studies showed that Leishmania major promastigotes are sensitive to osmotic conditions. A reduction in osmolality caused the cells to shorten and to rapidly release most of their large internal pool of alanine. In this study some effects of hyper-osmotic stress were examined. An increase in osmolality of the culture medium from 308 to 625 mOsm/kg caused only a small decrease in growth rate. When cells grown in the usual culture medium (308 mOsm/kg) were washed, resuspended in iso-osmotic buffer, and subjected to acute hyper-osmotic stress by addition of mannitol, the alanine content increased even in the absence of exogenous substrate. Promastigotes, depleted of alanine by a 5-min exposure to hypo-osmotic conditions, also synthesized alanine when resuspended in iso-osmotic buffer. Washed cells resuspended in iso-osmotic buffer consume their internal pool of alanine under aerobic conditions. Rates of consumption decreased on addition of mannitol, becoming zero at about 440 mOsm/kg. At higher osmolalities, alanine synthesis occurred. To estimate whether proteolysis could account for alanine synthesis in the absence of exogenous substrate, cells that had been grown with [1-14C]leucine were washed and resuspended under hypo-, iso-, and hyper-osmotic conditions and the amounts of 14CO2 and 14C-labelled peptides released in 1 h were measured. Little proteolysis occurred under these conditions, but the possibility that proteolysis was the source of the alanine increase, observed in response to hyper-osmotic stress, cannot be ruled out.
早期研究表明,硕大利什曼原虫前鞭毛体对渗透条件敏感。渗透压降低会导致细胞缩短,并迅速释放其大部分内部大量储存的丙氨酸。在本研究中,检测了高渗应激的一些影响。培养基渗透压从308 mOsm/kg增加到625 mOsm/kg仅导致生长速率略有下降。当在常规培养基(308 mOsm/kg)中生长的细胞被洗涤、重悬于等渗缓冲液中,并通过添加甘露醇使其受到急性高渗应激时,即使在没有外源底物的情况下,丙氨酸含量也会增加。通过5分钟的低渗条件处理耗尽丙氨酸的前鞭毛体,当重悬于等渗缓冲液中时也会合成丙氨酸。重悬于等渗缓冲液中的洗涤细胞在有氧条件下消耗其内部储存的丙氨酸。添加甘露醇后消耗速率降低,在约440 mOsm/kg时变为零。在更高的渗透压下,丙氨酸开始合成。为了评估在没有外源底物的情况下蛋白水解是否可以解释丙氨酸的合成,将用[1-14C]亮氨酸培养的细胞洗涤后,在低渗、等渗和高渗条件下重悬,并测量1小时内释放的14CO2和14C标记肽的量。在这些条件下几乎没有发生蛋白水解,但不能排除蛋白水解是高渗应激下观察到的丙氨酸增加的来源的可能性。