Oster Michael, Just Franziska, Büsing Kirsten, Wolf Petra, Polley Christian, Vollmar Brigitte, Muráni Eduard, Ponsuksili Siriluck, Wimmers Klaus
Leibniz Institute for Farm Animal Biology, Institute for Genome Biology, Dummerstorf, Germany;
University of Rostock, Nutrition Physiology and Animal Nutrition, Rostock, Germany; and.
Am J Physiol Regul Integr Comp Physiol. 2016 May 15;310(10):R917-25. doi: 10.1152/ajpregu.00215.2015. Epub 2016 Mar 9.
Phosphorus (P) is of vital importance for many aspects of metabolism, including bone mineralization, blood buffering, and energy utilization. In order to identify molecular routes affecting intrinsic P utilization, we address processes covering P intake, uptake, metabolism, and excretion. In particular, the interrelation of bone tissue and immune features is of interest to approximate P intake to animal's physiology and health status. German Landrace piglets received different levels of digestible phosphorus: recommended, higher, or lower amounts. At multiple time points, relevant serum parameters were analyzed and radiologic studies on bone characteristics were performed. Peripheral blood mononuclear cells were collected to assess differential gene expression. Dietary differences were reflected by serum phosphorus, calcium, parathyroid hormone, and vitamin D. Bone reorganization was persistently affected as shown by microstructural parameters, cathepsin K levels, and transcripts associated with bone formation. Moreover, blood expression patterns revealed a link to immune response, highlighting bidirectional loops comprising bone formation and immune features, where the receptor-activator of NF-κB ligand/receptor-activator of NF-κB kinase system may play a prominent role. The modulated P supplementation provoked considerable organismal plasticity. Genes found to be differentially expressed due to variable P supply are involved in pathways relevant to P utilization and are potential candidate genes for improved P efficiency.
磷(P)在新陈代谢的许多方面都至关重要,包括骨矿化、血液缓冲和能量利用。为了确定影响内源性磷利用的分子途径,我们研究了涵盖磷摄入、吸收、代谢和排泄的过程。特别值得关注的是骨组织与免疫特征之间的相互关系,以便使磷的摄入量与动物的生理和健康状况相匹配。德国长白仔猪接受了不同水平的可消化磷:推荐量、较高量或较低量。在多个时间点,分析了相关的血清参数,并对骨骼特征进行了放射学研究。收集外周血单核细胞以评估差异基因表达。血清磷、钙、甲状旁腺激素和维生素D反映了饮食差异。微观结构参数、组织蛋白酶K水平以及与骨形成相关的转录本表明,骨重塑持续受到影响。此外,血液表达模式揭示了与免疫反应的联系,突出了包括骨形成和免疫特征的双向循环,其中核因子κB受体激活蛋白配体/核因子κB激酶系统受体激活蛋白可能发挥重要作用。调节磷的补充引发了相当大的机体可塑性。因磷供应变化而差异表达的基因参与了与磷利用相关的途径,是提高磷效率的潜在候选基因。