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表皮生长因子可加速氧化剂损伤后LLC-PK1细胞的恢复。

Epidermal growth factor accelerates recovery of LLC-PK1 cells following oxidant injury.

作者信息

Andreoli S P, Mallett C P, McAteer J A, Kempson S A, Fineberg N

机构信息

Department of Pediatrics, Indiana University Medical Center, Indianapolis 46202, USA.

出版信息

In Vitro Cell Dev Biol Anim. 1998 Nov-Dec;34(10):824-30. doi: 10.1007/s11626-998-0037-6.

Abstract

In renal tubular epithelial cells, oxidant injury results in several metabolic alterations including ATP depletion, decreased Na+K+ATPase activity, and altered intracellular sodium and potassium content. To investigate the recovery of LLC-PK1 cells following oxidant injury and to determine if recovery can be accelerated, we induced oxidant stress in LLC-PK1 cells with 500 microM hydrogen peroxide for 60 min. Identical cohorts of oxidant-stressed cells were incubated in recovery medium without epidermal growth factor (EGF) or recovery medium containing 25 ng EGF per ml. ATP levels, Na+K+ATPase activity in whole cells, Na+K+ATPase activity in disrupted cells, and intracellular sodium and potassium ion content were determined at 0, 5, 24, 48, and 72 h following oxidant injury in each cohort of cells. In oxidant-stressed cells recovering in medium without EGF, ATP levels, Na+K+ATPase activity, and intracellular ion content improved but continued to remain substantially lower than control values at all time points following oxidant stress. In cells recovering in medium with EGF, ATP levels, Na+K+ATPase activity, and the intracellular potassium-to-sodium ratio were significantly higher at nearly all time points than values in cells recovering in medium alone. In cells recovering with added EGF, Na+K+ATPase activity had improved to control levels, whereas ATP levels and intracellular ion content approached control values by 72 h following oxidant stress. We conclude that oxidant-mediated ATP depletion, altered Na+K+ATPase activity, and intracellular ion content remain depressed for several d following oxidant stress and that EGF accelerated recovery of LLC-PK1 cells from oxidant injury.

摘要

在肾小管上皮细胞中,氧化损伤会导致多种代谢改变,包括ATP耗竭、Na+K+ATP酶活性降低以及细胞内钠和钾含量改变。为了研究LLC-PK1细胞在氧化损伤后的恢复情况,并确定恢复是否可以加速,我们用500微摩尔过氧化氢对LLC-PK1细胞诱导氧化应激60分钟。将相同批次的氧化应激细胞分别置于不含表皮生长因子(EGF)的恢复培养基或每毫升含25纳克EGF的恢复培养基中培养。在每组细胞氧化损伤后的0、5、24、48和72小时,测定ATP水平、全细胞Na+K+ATP酶活性、破碎细胞中的Na+K+ATP酶活性以及细胞内钠和钾离子含量。在不含EGF的培养基中恢复的氧化应激细胞,ATP水平、Na+K+ATP酶活性和细胞内离子含量有所改善,但在氧化应激后的所有时间点仍显著低于对照值。在含EGF的培养基中恢复的细胞,几乎在所有时间点,ATP水平、Na+K+ATP酶活性以及细胞内钾钠比均显著高于仅在培养基中恢复的细胞。在添加EGF恢复的细胞中,Na+K+ATP酶活性已恢复到对照水平,而ATP水平和细胞内离子含量在氧化应激后72小时接近对照值。我们得出结论,氧化应激介导的ATP耗竭、Na+K+ATP酶活性改变以及细胞内离子含量在氧化应激后数天仍处于较低水平,并且EGF可加速LLC-PK1细胞从氧化损伤中的恢复。

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