Department of Microbiology and Molecular Genetics, University of Pittsburgh , Pittsburgh, PA , USA.
Bristol Heart Institute and Bristol CardioVascular, Bristol Royal Infirmary, University of Bristol , Bristol , UK.
Front Immunol. 2014 Oct 9;5:478. doi: 10.3389/fimmu.2014.00478. eCollection 2014.
Science can move ahead by questioning established or canonical views and, so it may be with the enzymes, nitric oxide synthases (NOS). Nitric oxide (NO) is generated by NOS isoforms that are often described by their tissue-specific expression patterns. NOS1 (nNOS) is abundant in neural tissue, NOS2 is upregulated in activated macrophages and known as inducible NOS (iNOS), and NOS3 (eNOS) is abundant in endothelium where it regulates vascular tone. These isoforms are described as constitutive or inducible, but in this perspective we question the broad application of these labels. Are there instances where "constitutive" NOS (NOS1 and NOS3) are inducibly expressed; conversely, are there instances where NOS2 is constitutively expressed? NOS1 and NOS3 inducibility may be linked to post-translational regulation, making their actual patterns activity much more difficult to detect. Constitutive NOS2 expression has been observed in several tissues, especially the human pulmonary epithelium where it may regulate airway tone. These data suggest that expression of the three NOS enzymes may include non-established patterns. Such information should be useful in designing strategies to modulate these important enzymes in different disease states.
科学可以通过质疑既定或规范的观点向前发展,NOS 也可能如此。一氧化氮 (NO) 由 NOS 同工酶产生,这些同工酶通常根据其组织特异性表达模式来描述。NOS1(nNOS)在神经组织中丰富,NOS2 在活化的巨噬细胞中上调,称为诱导型 NOS(iNOS),NOS3(eNOS)在调节血管张力的内皮细胞中丰富。这些同工酶被描述为组成型或诱导型,但在这种观点下,我们质疑这些标签的广泛应用。是否存在“组成型”NOS(NOS1 和 NOS3)可诱导表达的情况;相反,是否存在 NOS2 组成型表达的情况?NOS1 和 NOS3 的诱导性可能与翻译后调节有关,这使得它们的实际活性模式更难检测。NOS2 的组成型表达已在几种组织中观察到,尤其是在人类肺上皮组织中,它可能调节气道张力。这些数据表明,三种 NOS 酶的表达可能包括非既定模式。这些信息对于设计在不同疾病状态下调节这些重要酶的策略可能是有用的。