Grunewald R W, Eckstein A, Reisse C H, Müller G A
Abteilung Nephrologie und Rheumatologie, Universitätsklinik Göttingen, Robert Koch Strasse 40, D-37075 Göttingen, Germany.
Nephron. 2001 Sep;89(1):73-81. doi: 10.1159/000046047.
The organic osmolyte sorbitol plays an important role in the osmoregulation of immortalized epithelial cells of the thick ascending limb of Henle's loop (TALH) of rabbit. The intracellular sorbitol content seems to depend strongly on the extracellular osmolarity. To investigate the nature of the osmotic regulation we characterized the aldose reductase.
We determined aldose reductase activity enzymatically and the content of organic osmolytes by HPLC.
The aldose reductase activity correlates with the extracellular tonicity. Elevating the osmolarity of the medium from 300 to 600 mosm/l by addition of NaCl or sucrose resulted in a significant increase of maximal velocity (V(max)) of the adapted cells from 8 +/- 1 micromol/g x min (300 mosm/l) to 322 +/- 28 micromol/g x min (600 mosm/l, NaCl) or 54 +/- 9 micromol/g x min (600 mosm/l, sucrose), respectively, while affinity (K(m)) remained unchanged. But we found no rise of aldose reductase activity when extracellular urea concentration was elevated. Similar alterations in V(max) were observed when the activity of the highly enriched enzyme was determined with glucose as substrate. Elevation of the extracellular osmolarity by NaCl and sucrose strongly induced the expression of aldose reductase protein with an apparent molecular weight of 39 kD. The affinity of glucose is characteristically low with a K(m) above 300 mmol/l. Aldose reductase utilizes both NADPH and with lower affinity NADH as coenzymes. In vitro sulfate ions (0.4 mol/l) results in a two-fold activation of the aldose reductase activity whereas sodium (200-400 mmol/l) decreased the activity significantly (22-33%). Potassium and chloride up to 400 mmol/l did not alter the aldose reductase activity in vitro.
These results indicate that the aldose reductase of TALH cells of the outer medulla is osmotically regulated and has many similarities with aldose reductase in renal inner medulla. Therefore, intracellular sorbitol synthesis seems to be of similar importance in the osmoregulation of TALH cells as in the inner medulla.
有机渗透质山梨醇在兔髓袢升支粗段(TALH)永生化上皮细胞的渗透调节中起重要作用。细胞内山梨醇含量似乎强烈依赖于细胞外渗透压。为了研究渗透调节的本质,我们对醛糖还原酶进行了特性分析。
我们通过酶法测定醛糖还原酶活性,并通过高效液相色谱法测定有机渗透质的含量。
醛糖还原酶活性与细胞外张力相关。通过添加氯化钠或蔗糖将培养基渗透压从300 mosm/l提高到600 mosm/l,导致适应细胞的最大速度(V(max))显著增加,从8±1微摩尔/克·分钟(300 mosm/l)分别增加到322±28微摩尔/克·分钟(600 mosm/l,氯化钠)或54±9微摩尔/克·分钟(600 mosm/l,蔗糖),而亲和力(K(m))保持不变。但当细胞外尿素浓度升高时,我们未发现醛糖还原酶活性增加。当以葡萄糖为底物测定高度纯化酶的活性时,观察到V(max)有类似变化。氯化钠和蔗糖使细胞外渗透压升高强烈诱导了表观分子量为39 kD的醛糖还原酶蛋白的表达。葡萄糖的亲和力特征性地较低,K(m)高于300 mmol/l。醛糖还原酶利用NADPH以及亲和力较低的NADH作为辅酶。体外实验中,硫酸根离子(0.4 mol/l)使醛糖还原酶活性提高两倍,而钠离子(200 - 400 mmol/l)显著降低活性(22 - 33%)。钾离子和氯离子浓度高达400 mmol/l时,在体外未改变醛糖还原酶活性。
这些结果表明,外髓TALH细胞的醛糖还原酶受渗透压调节,并且与肾内髓中的醛糖还原酶有许多相似之处。因此,细胞内山梨醇合成在TALH细胞的渗透调节中似乎与在内髓中具有相似的重要性。