Hoet P H, Dinsdale D, Lewis C P, Verbeken E K, Lauweryns J M, Nemery B
Laboratory of Pneumology, KU Leuven, Belgium.
Thorax. 1993 Dec;48(12):1235-41. doi: 10.1136/thx.48.12.1235.
The polyamines (putrescine, spermidine, and spermine) are involved in cellular growth, proliferation, and differentiation. In the lungs of various species, polyamines are accumulated by an active uptake system which also mediates the uptake of cystamine and paraquat. In the rat lung putrescine uptake has been shown to be cell-specific, occurring predominantly in the alveolar epithelium. The aim of this study was to characterise the uptake of putrescine in human lung.
Lung tissue was obtained from 31 patients undergoing surgery for lung cancer. Slices (0.7 mm thick) from non-tumour containing lung parenchyma were incubated for 15-60 minutes in Krebs-Ringer phosphate buffer with various concentrations of putrescine (2.5 to 80 mumol/l) containing 0.1 microCi [1,4-14C]-putrescine. Uptake was assessed from tissue radioactivity. For autoradiographic imaging, slices were incubated for 30 minutes with 2.5 mumol/l putrescine containing 2.5 mCi [1,4n-3H]-putrescine.
The accumulation of [14C]-putrescine into slices was time-dependent and energy-dependent, and obeyed saturation kinetics, with mean calculated values for Vmax (maximal rate of uptake) of 414 nmol/g/hour and for Km (medium concentration at which the rate of uptake is half Vmax) of 7.2 mumol/l, with a large interindividual variation. Competitive inhibition was observed on incubation with cystamine, which appears to have a high affinity for the uptake system since its calculated Ki (concentration of inhibitor at which the Km is doubled) was 3.2 mumol/l. Ultrastructural autoradiography showed labelling over both type I and type II cells of the alveolar epithelium, but not over the endothelium or any cells of the interstitium. Alveolar macrophages were also devoid of label.
These results show that the human lung possesses an active uptake system for putrescine, and probably also cystamine, which is located in both cell types of the alveolar epithelium. These findings may be used to develop tests for the assessment of the alveolar epithelium.
多胺(腐胺、亚精胺和精胺)参与细胞生长、增殖和分化。在各种物种的肺中,多胺通过一种主动摄取系统积累,该系统也介导胱胺和百草枯的摄取。在大鼠肺中,已表明腐胺摄取具有细胞特异性,主要发生在肺泡上皮细胞。本研究的目的是表征人肺中腐胺的摄取情况。
从31例接受肺癌手术的患者获取肺组织。将不含肿瘤的肺实质切成0.7毫米厚的切片,在含有不同浓度腐胺(2.5至80微摩尔/升)且含有0.1微居里[1,4 - 14C] - 腐胺的 Krebs - Ringer 磷酸盐缓冲液中孵育15 - 60分钟。通过组织放射性评估摄取情况。对于放射自显影成像,将切片与含有2.5毫居里[1,4n - 3H] - 腐胺的2.5微摩尔/升腐胺孵育30分钟。
[14C] - 腐胺在切片中的积累是时间依赖性和能量依赖性的,并且符合饱和动力学,Vmax(最大摄取速率)的平均计算值为414纳摩尔/克/小时,Km(摄取速率为Vmax一半时的介质浓度)为7.2微摩尔/升,个体间差异较大。与胱胺孵育时观察到竞争性抑制,由于其计算的Ki(使Km加倍的抑制剂浓度)为3.2微摩尔/升,胱胺似乎对摄取系统具有高亲和力。超微结构放射自显影显示肺泡上皮的I型和II型细胞均有标记,但内皮或间质的任何细胞均无标记。肺泡巨噬细胞也无标记。
这些结果表明人肺具有腐胺以及可能还有胱胺的主动摄取系统,该系统位于肺泡上皮的两种细胞类型中。这些发现可用于开发评估肺泡上皮的检测方法。