首页> 外文期刊>Photochemistry and Photobiology: An International Journal >PREPROGRAMMED AND PROGRAMMED CELL DEATH MECHANISMS OF APOPTOSIS - UV-INDUCED IMMEDIATE AND DELAYED APOPTOSIS
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PREPROGRAMMED AND PROGRAMMED CELL DEATH MECHANISMS OF APOPTOSIS - UV-INDUCED IMMEDIATE AND DELAYED APOPTOSIS

机译:预先编程和程序化的细胞死亡机制-紫外线诱导的立即和延迟凋亡

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摘要

Equitoxic doses (10% clonogenic survival) of UV radiation (UVR) from the three waveband regions, i.e. UVA1 (340-400 nm), UVB (290-320 nm) and UVC (200-290 nm), were shown to induce immediate or delayed apoptosis in L5178Y-R murine lymphoma cells, Membrane and DNA damage were shown to be the most probable initiators of UVA1-induced immediate or UVR-induced delayed apoptosis, respectively, These UV-induced apoptotic processes appeared to utilize two different ''core'' biochemical mechanisms; however, one core mechanism could be initiated at two distinct sites (e.g. membrane or DNA) and result in disparate kinetics, In an attempt to resolve this mechanistic issue, the dependence on macromolecular synthesis of each UV-induced apoptotic mechanism was investigated, In the absence of UVR, inhibition of either transcription (actinomycin D) or translation (cycloheximide) induced apoptosis in a concentration- and time-dependent manner. These results suggest that an apoptotic mechanism exists that does not require macromolecular synthesis postinsult (constitutive), The UVR data demonstrate that UVA1-induced immediate apoptosis utilizes this constitutive mechanism (preprogrammed), while UVR-induced delayed apoptosis utilizes the well-known inducible mechanism (programmed), Therefore, there are two different core biochemical mechanisms of apoptotic death available to each cell: preprogrammed (constitutive) and programmed (inducible) cell death. [References: 38]
机译:研究表明,来自三个波段的紫外线辐射(UVR1)(340-400 nm),UVB(290-320 nm)和UVC(200-290 nm)的等毒剂量(10%克隆形成存活)。或L5178Y-R鼠淋巴瘤细胞的凋亡延迟或延迟凋亡,膜和DNA损伤分别是UVA1诱导的立即凋亡或UVR诱导的延迟凋亡的最可能引发剂,这些UV诱导的凋亡过程似乎利用了两种不同的''核心''生化机制;然而,一种核心机制可能在两个不同的位点(例如膜或DNA)启动,并导致完全不同的动力学。为解决这一机理问题,研究了每种紫外线诱导的凋亡机制对大分子合成的依赖性。在没有UVR的情况下,转录(放线菌素D)或翻译(环己酰亚胺)的抑制以浓度和时间依赖性方式诱导凋亡。这些结果表明存在不需要大分子合成后凋亡的机制(本构)。UVR数据表明,UVA1诱导的立即凋亡利用了这种本构机制(预先编程),而UVR诱导的延迟凋亡利用了众所周知的诱导机制。 (编程的),因此,每个细胞有两种不同的凋亡死亡核心生化机制:预编程的(组成性)和程序性的(诱导性)细胞死亡。 [参考:38]

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