McLennan A G
School of Biological Sciences, Life Sciences Building, University of Liverpool, Crown Street, L69 7ZB, Liverpool, UK.
Pharmacol Ther. 2000 Aug-Sep;87(2-3):73-89. doi: 10.1016/s0163-7258(00)00041-3.
Despite being known for over 30 years, the functions of the dinucleoside polyphosphates, such as diadenosine 5',5"'-P(1), P(4)-tetraphosphate (Ap(4)A) and diadenosine 5',5"'-P(1), P(3)-triphosphate (Ap(3)A), are still unclear. On the one hand, they may have important signalling functions, both inside and outside the cell (friend), while on the other hand, they may simply be the unavoidable by-products of certain biochemical reactions, which, if allowed to accumulate, would be potentially toxic through their structural similarity to ATP and other essential mononucleotides (foe). Here, the occurrence, synthesis, degradation, and proposed functions of these compounds are briefly reviewed, along with some new data and recent evidence supporting roles for Ap(3)A and Ap(4)A in the cellular decision making processes leading to proliferation, quiescence, differentiation, and apoptosis. Hypotheses are forwarded for the involvement of Ap(4)A in the intra-S phase DNA damage checkpoint and for Ap(3)A and the pFhit (fragile histidine triad gene product) protein in tumour suppression. It is concluded that the roles of friend and foe are not incompatible, but are distinguished by the concentration range of nucleotide achieved under different circumstances.
尽管二核苷多磷酸(如5',5'''-P(1),P(4)-四磷酸二腺苷(Ap(4)A)和5',5'''-P(1),P(3)-三磷酸二腺苷(Ap(3)A))已被发现30多年,但它们的功能仍不明确。一方面,它们可能在细胞内外具有重要的信号传导功能(有益作用),而另一方面,它们可能仅仅是某些生化反应不可避免的副产物,如果任其积累,由于其与ATP和其他必需单核苷酸结构相似,可能具有潜在毒性(有害作用)。本文简要综述了这些化合物的存在、合成、降解及推测的功能,以及一些支持Ap(3)A和Ap(4)A在导致细胞增殖、静止、分化和凋亡的细胞决策过程中发挥作用的新数据和最新证据。文中还提出了关于Ap(4)A参与S期内DNA损伤检查点以及Ap(3)A和pFhit(脆性组氨酸三联体基因产物)蛋白参与肿瘤抑制的假说。得出的结论是,有益作用和有害作用并非不相容,而是由不同情况下达到的核苷酸浓度范围所区分。