Khaled A. Al‐Hosaini, S. Bloom, J. Hedrick, A. Howard, P. Jethwa, S. Luckman, R. Raddatz, N. Semjonous, G. Willars
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引用次数: 0
摘要
神经质素U受体(NC-IUPHAR[30]推荐的临时命名)被内源性25个氨基酸肽神经质素U (Neuromedin U-25, NmU-25)激活,该肽最初从猪脊髓中分离出来[92]。在人类中,NMU -25似乎是前体基因(NMU, P48645)的唯一产物,具有广泛的组织分布,但在上胃肠道、中枢神经系统、骨髓和胎儿肝脏中表达水平最高。在某些物种中发现了更短版本的NmU,但在人类中没有,并且至少在某些情况下是由较长的NmU的蛋白水解裂解产生的。尽管NmU结构存在物种差异,但c端区域(特别是c端五肽)高度保守,并具有生物活性。Neuromedin S (Neuromedin S-33)也被确定为内源性激动剂[97]。NmS-33,顾名思义,是源自单个基因的前体蛋白的33个氨基酸产物,含有与NmU相同的修饰过的c端七肽。NmS-33激活NMU受体的效力与NMU -25相当。
Neuromedin U receptors (provisional nomenclature as recommended by NC-IUPHAR [30]) are activated by the endogenous 25 amino acid peptide neuromedin U (neuromedin U-25, NmU-25), a peptide originally isolated from pig spinal cord [92]. In humans, NmU-25 appears to be the sole product of a precursor gene (NMU, P48645) showing a broad tissue distribution, but which is expressed at highest levels in the upper gastrointestinal tract, CNS, bone marrow and fetal liver. Much shorter versions of NmU are found in some species, but not in human, and are derived at least in some instances from the proteolytic cleavage of the longer NmU. Despite species differences in NmU structure, the C-terminal region (particularly the C-terminal pentapeptide) is highly conserved and contains biological activity. Neuromedin S (neuromedin S-33) has also been identified as an endogenous agonist [97]. NmS-33 is, as its name suggests, a 33 amino-acid product of a precursor protein derived from a single gene and contains an amidated C-terminal heptapeptide identical to NmU. NmS-33 appears to activate NMU receptors with equivalent potency to NmU-25.