Campbell F M, Dutta-Roy A K
Rowett Research Institute, Bucksburn, Aberdeen, Scotland, UK.
FEBS Lett. 1995 Nov 20;375(3):227-30. doi: 10.1016/0014-5793(95)01216-2.
We reported earlier the presence of a 40 kDa plasma membrane fatty acid-binding protein (FABPpm) in human placenta. This protein is thought to be involved in the sequestration of unesterified free fatty acids bound to albumin from the maternal plasma for delivery to the fetus. However, its location in human placental syncytiotrophoblasts is not known. These cells are bipolar; one side facing maternal circulation (microvillous membranes), and the other side facing fetal circulation (basal membranes). Therefore, it is important to resolve the location of this protein in trophoblast membranes in order to understand fatty acid transport and metabolism in human placenta. Isolated plasma membranes vesicles were prepared respectively from the maternal facing microvillous and fetal facing surface of the human full-term placental syncytiotrophoblast. Using these membrane preparations, fatty acid binding activity, the polyacrylamide gel electrophoresis radiobinding assay for FABPpm, and Western blot analysis of FABPpm were carried out to determine the location of this protein in these membranes. Based on the above studies we conclude that the FABPpm is located exclusively in the microvillous membranes. Since FABPpm may be responsible for FFA uptake, its location in the microvillous membranes favours the unidirectional flow of maternal FFA to the fetus.
我们之前报道过人胎盘中存在一种40 kDa的质膜脂肪酸结合蛋白(FABPpm)。这种蛋白被认为参与了从母体血浆中隔离与白蛋白结合的未酯化游离脂肪酸,并将其输送给胎儿的过程。然而,其在人胎盘合体滋养层细胞中的定位尚不清楚。这些细胞是双极的,一侧面向母体循环(微绒毛膜),另一侧面向胎儿循环(基底膜)。因此,确定该蛋白在滋养层细胞膜中的位置对于理解人胎盘中脂肪酸的运输和代谢至关重要。分别从人足月胎盘合体滋养层面向母体的微绒毛表面和面向胎儿的表面制备了分离的质膜囊泡。利用这些膜制剂,进行了脂肪酸结合活性、FABPpm的聚丙烯酰胺凝胶电泳放射结合测定以及FABPpm的蛋白质印迹分析,以确定该蛋白在这些膜中的位置。基于上述研究,我们得出结论,FABPpm仅位于微绒毛膜中。由于FABPpm可能负责游离脂肪酸的摄取,其在微绒毛膜中的定位有利于母体游离脂肪酸向胎儿的单向流动。