Hamada Y
Department of Periodontology, School of Dentistry, Kagoshima University, Japan.
J Dent Res. 1996 Apr;75(4):1002-7. doi: 10.1177/00220345960750040101.
Actinomyces amphiphile (AcA) is an amphipathic molecule produced by Actinomyces viscosus that exhibits several biological activities. The effect of AcA on the fluidity and permeability of the plasma membrane in human umbilical vein endothelial cells was analyzed by a spin label method with 5- and 16-stearic acid nitroxide labels (SAL). These labels help to visualize the fluidity at the shallow (5-SAL) and deep (16-SAL) portions of the lipid bilayer. Cells were incubated with and without AcA (control) at 37 degrees C for 6 hours, and membrane fluidity was periodically measured. Another spin label, 4-(N, N-dimethyl-N-hexadecyl) ammonium-2, 2, 6, 6-tetramethyl-piperidine-1-oxyliodine (CAT-16), was also used to assess the physical state of the cell surface. The order parameter of 5-SAL was significantly lower in the cells incubated with AcA than in control cells after the six-hour incubation. The motion parameter of 16-SAL was significantly lower in AcA-treated cells than in controls after 4 and 6 hours of incubation. These findings indicated that the AcA increased the fluidity. There were no significant differences between the AcA-treated and control cells incubated for only 2 hours. In addition, there were no differences in CAT-16 measurements between AcA-treated and control cells. The release of endoplasmic lactate dehydrogenase (LDH) into the medium tended to increase in the AcA-treated vs. the control cells. LDH release increased in both a dose- and time-dependent manner, indicating that AcA increased the permeability of plasma membranes. These findings suggest that AcA alters the biophysical properties of the plasma membranes of endothelial cells, affecting membrane function.
嗜两亲放线菌(AcA)是黏性放线菌产生的一种两亲性分子,具有多种生物学活性。采用自旋标记法,利用5-和16-硬脂酸氮氧化物标记(SAL)分析了AcA对人脐静脉内皮细胞质膜流动性和通透性的影响。这些标记有助于观察脂质双层浅部(5-SAL)和深部(16-SAL)的流动性。将细胞在37℃下分别与AcA共同孵育和不与AcA共同孵育(对照)6小时,并定期测量膜流动性。另一种自旋标记物4-(N,N-二甲基-N-十六烷基)铵-2,2,6,6-四甲基哌啶-1-氧碘化物(CAT-16)也用于评估细胞表面的物理状态。孵育6小时后,与AcA共同孵育的细胞中5-SAL的序参数显著低于对照细胞。孵育4小时和6小时后,经AcA处理的细胞中16-SAL的运动参数显著低于对照细胞。这些发现表明AcA增加了流动性。仅孵育2小时的AcA处理细胞和对照细胞之间没有显著差异。此外,AcA处理细胞和对照细胞在CAT-16测量方面没有差异。与对照细胞相比,经AcA处理的细胞中内质乳酸脱氢酶(LDH)向培养基中的释放倾向于增加。LDH释放呈剂量和时间依赖性增加,表明AcA增加了质膜的通透性。这些发现表明AcA改变了内皮细胞质膜的生物物理性质,影响膜功能。