Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
J Neurochem. 2010 Jun;113(5):1275-84. doi: 10.1111/j.1471-4159.2010.06706.x. Epub 2010 Mar 26.
Mice with a targeted mutation in proSAAS have been generated to investigate whether peptides derived from this precursor could function as an inhibitor of prohormone convertase 1/3 (PC1/3) in vivo as well as to determine any alternate roles for proSAAS in nervous and endocrine tissues. Fetal mice lacking proSAAS exhibit complete, adult-like processing of prodynorphin in the prenatal brain instead of the incomplete processing seen in the brains of wild-type fetal mice where inhibitory proSAAS intermediates are transiently accumulated. This study provides evidence that proSAAS is directly involved in the prenatal regulation of neuropeptide processing in vivo. However, adult mice lacking proSAAS have normal levels of all peptides detected using a peptidomics approach, suggesting that PC1/3 activity is not affected by the absence of proSAAS in adult mice. ProSAAS knockout mice exhibit decreased locomotion and a male-specific 10-15% decrease in body weight, but maintain normal fasting blood glucose levels and are able to efficiently clear glucose from the blood in response to a glucose challenge. This work suggests that proSAAS-derived peptides can inhibit PC1/3 in embryonic brain, but in the adult brain proSAAS peptides may function as neuropeptides that regulate body weight and potentially other behaviors.
已生成靶向突变 proSAAS 的小鼠,以研究该前体衍生的肽是否可作为体内前激素转化酶 1/3(PC1/3)的抑制剂,以及确定 proSAAS 在神经和内分泌组织中的任何其他作用。缺乏 proSAAS 的胎儿小鼠在产前大脑中表现出完整的、成人样的 prodynorphin 加工,而不是在野生型胎儿小鼠的大脑中看到的不完全加工,其中抑制性 proSAAS 中间产物是暂时积累的。这项研究提供了证据表明 proSAAS 直接参与体内神经肽加工的产前调节。然而,缺乏 proSAAS 的成年小鼠使用肽组学方法检测到的所有肽的水平均正常,表明 PC1/3 活性不受成年小鼠中 proSAAS 缺失的影响。ProSAAS 敲除小鼠表现出运动减少和雄性特异性 10-15%的体重减轻,但保持正常的空腹血糖水平,并能够有效地清除血液中的葡萄糖以响应葡萄糖挑战。这项工作表明,proSAAS 衍生的肽可抑制胚胎脑中的 PC1/3,但在成人大脑中,proSAAS 肽可能作为调节体重和潜在其他行为的神经肽发挥作用。