Pittman Quentin J, Hollenberg Morley D
Gen Comp Endocrinol. 2009 Oct;164(1):7-14. doi: 10.1016/j.ygcen.2009.04.024. Epub 2009 May 4.
From the individual perspective of the two authors who were long-time colleagues of Karl Lederis at the University of Calgary, the events and personal interactions are described, that are relevant to the discovery of Urotensin I (UI) in the Lederis laboratory, along with the concurrent discovery of Urotensin II (UII) in the Bern laboratory and corticotropin-releasing factor (CRF/CRH) in the Vale laboratory. The fortuitous sabbatical experiences that put Professors Lederis and Bern on the track of the Urotensins, along with the essential isolation paradigm that resulted in the complete sequencing and synthesis of UI and UII are summarized. The chance interaction between Drs. Vale and Lederis who, prior to the publications of the sequences of UI and CRF, realized the sequence commonalities of these peptides with the vasoactive frog peptide, sauvagine, is outlined. Further, the relationship between the pharmacological studies done with UI in the Calgary laboratory and the more recent understanding of the biology and receptor pharmacology for the entire Urotensin I-CRF-Urocortin peptide family is dealt with. The value of a comparative endocrinology approach to understanding hormone action is emphasized, along with a projection to the future, based on new hypotheses that can be generated by unexplained data already in the literature. Based on the previously described pharmacology of the UI-CRF-Urocortin peptides in a number of target tissues, it is suggested that the use of current molecular approaches can be integrated with a 'classical' pharmacological approach to generate new insights about the UI-CRF-Urocortin hormone family.
从卡尔加里大学卡尔·莱德里斯的两位长期同事的个人视角出发,描述了与莱德里斯实验室中尿紧张素I(UI)的发现相关的事件和个人互动,同时也提到了伯尔尼实验室中尿紧张素II(UII)以及瓦尔实验室中促肾上腺皮质激素释放因子(CRF/CRH)的同期发现。总结了使莱德里斯教授和伯尔尼教授踏上尿紧张素研究之路的偶然休假经历,以及导致UI和UII完全测序与合成的关键分离范式。概述了瓦尔博士和莱德里斯博士之间的偶然互动,即在UI和CRF序列发表之前,他们就意识到这些肽与血管活性蛙肽蛙皮素的序列共性。此外,还讨论了卡尔加里实验室对UI进行的药理学研究与对整个尿紧张素I - CRF - 尿皮质素肽家族生物学和受体药理学的最新认识之间的关系。强调了比较内分泌学方法在理解激素作用方面的价值,并基于文献中已有但未解释的数据所产生的新假设对未来进行了展望。基于先前描述的UI - CRF - 尿皮质素肽在多个靶组织中的药理学,建议将当前的分子方法与“经典”药理学方法相结合,可以对UI - CRF - 尿皮质素激素家族产生新的见解。