Cammarata P R, Tse D, Yorio T
Department of Anatomy and Cell Biology, Texas College of Osteopathic Medicine, Fort Worth 76107.
Curr Eye Res. 1990 Jun;9(6):561-8. doi: 10.3109/02713689008999596.
The synthesis of phosphatidylinositol, phosphatidylinositol-4-phosphate and phosphatidylinositol-4-5-bisphosphate was studied using 3H-myo-inositol (3H-MI) as precursor in cultured bovine lens epithelial cells (BLECs) maintained in galactose-free, physiological medium or 40 mM galactose (Gal) +/- sorbinil for six days. The formation of inositol polyphosphates from phosphoinositides was also shown. Galactitol did not exceed 2mM in Gal-incubated cells after six days of exposure; no galactitol was observed in BLECs maintained in galactose-free, physiological medium or Gal supplemented with sorbinil. Uptake of 3H-myo-inositol(3H-MI) into BLECs was significantly reduced in cells exposed to Gal. A concomitant reduction in 3H-MI incorporation was observed in the phosphoinositides, as well as with the released inositol phosphates. The simultaneous addition of sorbinil to the Gal medium corrected the drop in 3H-MI uptake and normalized 3H-MI incorporation into the phosphoinositides and inositol phosphates. While an apparent decrease in the three inositol-containing lipids was observed with the Gal-incubated cells, based on 3H-MI incorporation, there was no change in total membrane phosphatidylinositol content when compared to cells maintained in physiological medium as determined by the microgram Pl PO4 per microgram total membrane PO4. The apparent loss of radiolabeled phosphoinositides was attributed to the decreased specific activity resulting from the lower internal pool of 3H-MI in the Gal-exposed cells available for incorporation into the phosphoinositides.(ABSTRACT TRUNCATED AT 250 WORDS)
在无半乳糖的生理培养基或含40 mM半乳糖(Gal)±索比尼尔的条件下,将培养的牛晶状体上皮细胞(BLECs)维持6天,以3H-肌醇(3H-MI)作为前体,研究了磷脂酰肌醇、磷脂酰肌醇-4-磷酸和磷脂酰肌醇-4,5-二磷酸的合成。还展示了从磷酸肌醇形成肌醇多磷酸的过程。暴露6天后,Gal孵育的细胞中半乳糖醇不超过2 mM;在无半乳糖的生理培养基或添加了索比尼尔的Gal培养基中培养的BLECs中未观察到半乳糖醇。暴露于Gal的细胞中,3H-肌醇(3H-MI)进入BLECs的摄取显著减少。在磷酸肌醇以及释放的肌醇磷酸中观察到3H-MI掺入量同时减少。向Gal培养基中同时添加索比尼尔可纠正3H-MI摄取的下降,并使3H-MI掺入磷酸肌醇和肌醇磷酸的量正常化。虽然Gal孵育的细胞中三种含肌醇的脂质基于3H-MI掺入量明显减少,但与在生理培养基中培养的细胞相比,通过每微克总膜PO4中微克Pl PO4测定,总膜磷脂酰肌醇含量没有变化。放射性标记的磷酸肌醇的明显损失归因于Gal暴露细胞中可用于掺入磷酸肌醇的3H-MI内部池较低导致的比活性降低。(摘要截断于250字)