Richardson D R, Dickson L, Baker E
Lady Davis Institute for Medical Research, Sir Morlimer B. Davis-Jewish General Hospital, Montréal, Québec, Canada.
In Vitro Cell Dev Biol Anim. 1996 Sep;32(8):486-95. doi: 10.1007/BF02723052.
A previous study described a cytoplasmic, transferrin (Tf)-free, iron (Fe) pool that was detected only when cells were mechanically detached from the culture substratum at 4 degrees C, after initial incubation with 59Fe-125I-Tf at 37 degrees C (Richardson and Baker, 1992a). The release of this internalized 59Fe could be markedly reduced if the cells were treated with proteases or incubated at 37 degrees C prior to detachment. The present study was designed to characterize this Fe pool and understand the mechanism of its release. The results show that cellular 59Fe release increased linearly as a function of preincubation time with 59Fe-Tf subsequent to mechanical detachment at 4 degrees C using a spatula. These data suggest that the 59Fe release was largely composed of end product(s) and was not an "intermediate Fe pool." When the Fe(II) chelator, dipyridyl (DP), was incubated with 59Fe-Tf and the cells, it prevented the accumulation of 59Fe that was released following mechanical detachment at 4 degrees C. Other chelators had much less effect on the proportion of 59Fe released. Examination of the 59Fe released showed that after a 4-h preincubation with 59Fe-Tf, approximately 50% of the 59Fe was present in ferritin. These data indicate that mechanical detachment of cells at 4 degrees C resulted in membrane disruptions that allow the release of high M(r), molecules. Moreover, electron microscopy studies showed that detachment of cells from the substratum at 4 degrees C resulted in pronounced membrane damage. In contrast, when cells were detached at 37 degrees C, or at 4 degrees C after treatment with pronase, membrane damage was minimal or not apparent. These results may imply that temperature-dependent processes prevent the release of intracellular contents on membrane wounding, or alternatively, prevent wounding at 37 degrees C. The evidence also indicates that caution is required when interpreting data from experiments where cells have been mechanically detached at 4 degrees C.
先前的一项研究描述了一种细胞质内不含转铁蛋白(Tf)的铁(Fe)池,该铁池只有在细胞于37℃用59Fe-125I-Tf预孵育后,于4℃从培养底物上机械分离时才能检测到(Richardson和Baker,1992a)。如果细胞在用蛋白酶处理后或在分离前于37℃孵育,这种内化的59Fe的释放会显著减少。本研究旨在表征这个铁池并了解其释放机制。结果表明,在用刮刀于4℃机械分离后,细胞内59Fe的释放随着与59Fe-Tf预孵育时间呈线性增加。这些数据表明,59Fe的释放主要由终产物组成,并非“中间铁池”。当铁(II)螯合剂联吡啶(DP)与59Fe-Tf和细胞一起孵育时,它能阻止在4℃机械分离后释放的59Fe的积累。其他螯合剂对59Fe释放比例的影响要小得多。对释放的59Fe的检测表明,在与59Fe-Tf预孵育4小时后,约50%的59Fe存在于铁蛋白中。这些数据表明,细胞在4℃机械分离会导致膜破坏,从而使高分子量分子得以释放。此外,电子显微镜研究表明,细胞在4℃从底物上分离会导致明显的膜损伤。相反,当细胞在37℃分离,或在用链霉蛋白酶处理后于4℃分离时,膜损伤最小或不明显。这些结果可能意味着温度依赖性过程可防止膜损伤时细胞内物质的释放,或者相反,可防止在37℃时造成损伤。证据还表明,在解释细胞于4℃机械分离的实验数据时需要谨慎。