Beggs Megan R, Alexander R Todd
1 Department of Physiology, University of Alberta, Edmonton, Alberta T6G 2R7, Canada.
2 Department of Pediatrics, University of Alberta, Edmonton, Alberta T6G 2R7, Canada.
Exp Biol Med (Maywood). 2017 Apr;242(8):840-849. doi: 10.1177/1535370217699536.
Calcium is vital for many physiological functions including bone mineralization. Postnatal deposition of calcium into bone is greatest in infancy and continues through childhood and adolescence until peek mineral density is reached in early adulthood. Thereafter, bone mineral density remains static until it eventually declines in later life. A positive calcium balance, i.e. more calcium absorbed than excreted, is crucial to bone deposition during growth and thus to peek bone mineral density. Dietary calcium is absorbed from the intestine into the blood. It is then filtered by the renal glomerulus and either reabsorbed by the tubule or excreted in the urine. Calcium can be (re)absorbed across intestinal and renal epithelia via both transcellular and paracellular pathways. Current evidence suggests that significant intestinal and renal calcium transport changes occur throughout development. However, the molecular details of these alterations are incompletely delineated. Here we first briefly review the current model of calcium transport in the intestine and renal tubule in the adult. Then, we describe what is known with regard to calcium handling through postnatal development, and how alterations may aid in mediating a positive calcium balance. The role of transcellular and paracellular calcium transport pathways and the contribution of specific intestinal and tubular segments vary with age. However, the current literature highlights knowledge gaps in how specifically intestinal and renal calcium (re)absorption occurs early in postnatal development. Future research should clarify the specific changes in calcium transport throughout early postnatal development including mediators of these alterations enabling appropriate bone mineralization. Impact statement This mini review outlines the current state of knowledge pertaining to the molecules and mechanisms maintaining a positive calcium balance throughout postnatal development. This process is essential to achieving optimal bone mineral density in early adulthood, thereby lowering the lifetime risk of osteoporosis.
钙对包括骨矿化在内的许多生理功能至关重要。出生后钙在骨骼中的沉积在婴儿期最大,并持续贯穿儿童期和青春期,直至成年早期达到峰值骨密度。此后,骨密度保持稳定,直到晚年最终下降。钙的正平衡,即吸收的钙多于排泄的钙,对于生长期间的骨沉积以及峰值骨密度至关重要。膳食钙从肠道吸收进入血液。然后它被肾小球过滤,要么被肾小管重吸收,要么随尿液排出。钙可以通过跨细胞和细胞旁途径在肠道和肾上皮细胞中(再)吸收。目前的证据表明,在整个发育过程中,肠道和肾脏的钙转运发生了显著变化。然而,这些改变的分子细节尚未完全阐明。在这里,我们首先简要回顾一下成人肠道和肾小管中钙转运的当前模型。然后,我们描述了关于出生后发育过程中钙处理的已知情况,以及这些改变如何有助于调节钙的正平衡。跨细胞和细胞旁钙转运途径的作用以及特定肠道和肾小管节段的贡献随年龄而变化。然而,目前的文献突出了出生后早期肠道和肾脏钙(再)吸收具体发生方式方面的知识空白。未来的研究应阐明出生后早期钙转运的具体变化,包括这些改变的介质,以实现适当的骨矿化。影响声明 本综述概述了关于出生后发育过程中维持钙正平衡的分子和机制的当前知识状态。这一过程对于在成年早期实现最佳骨密度至关重要,从而降低骨质疏松症的终生风险。