Eaton B M, Richards R C, Contractor S F
J Dev Physiol. 1987 Feb;9(1):69-78.
Uptake of 125I-labelled epidermal growth factor into trophoblast, and its subsequent fate, was studied in an isolated dually-perfused lobule of term human placenta. 125I-EGF added into the maternal circulation was rapidly taken up into the placental tissue where a portion was degraded and most of the breakdown products released back into the maternal circuit. At the end of the 2 h perfusion, radioactivity in the tissue accounted for 52% of the initial dose. 12.9% of the radioactivity remaining in the maternal circuit at the end of the perfusion, amounting to only 5.2% of the initial activity, could be identified as intact EGF by immunoaffinity chromatography. About 45 min after the start of the perfusion there was a sustained rise in the 125I activity in the fetal circulation accounting for 4.6% of the initial activity, and a small proportion of this (0.22% of the dose) could be immunologically characterised as EGF. In the presence of the acidotrophic agent chloroquine, there was a similar rapid clearance from the maternal circulation, which was not associated with breakdown. The tissue retention was slightly enhanced and there was very little transfer of activity into the fetal circulation.
在足月人胎盘的分离双灌注小叶中,研究了125I标记的表皮生长因子被滋养层摄取及其后续命运。添加到母体循环中的125I - EGF迅速被胎盘组织摄取,其中一部分被降解,大部分分解产物释放回母体循环。在2小时灌注结束时,组织中的放射性占初始剂量的52%。灌注结束时,母体循环中剩余的放射性中有12.9%,仅占初始活性的5.2%,可通过免疫亲和色谱法鉴定为完整的EGF。灌注开始约45分钟后,胎儿循环中的125I活性持续上升,占初始活性的4.6%,其中一小部分(剂量的0.22%)可通过免疫学鉴定为EGF。在存在酸营养剂氯喹的情况下,母体循环中的清除同样迅速,且与分解无关。组织保留略有增强,活性很少转移到胎儿循环中。