Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, 1100 S Grand Blvd, Saint Louis, MO 63104, USA.
Nutrients. 2024 Sep 28;16(19):3289. doi: 10.3390/nu16193289.
Milk production during lactation places a high demand for calcium that is fulfilled both from maternal bone resorption and diet. While it is known that mammary gland-derived PTHrP drives bone resorption during lactation, the impact of postpartum estrogen loss on bone has been unclear. We used a case-control study design to test the effect of estrogen loss in lactating mice. Results: In the present study, we show for the first time that estrogen loss during lactation activates memory T-cells (T) to produce TNFα and IL-17A to aid in bone resorption and calcium release. Our studies reveal a new mechanism for the release of calcium from bone postpartum. The findings provide several new insights. First, the immune system plays a critical role in milk production postpartum. Second, evolutionarily, the pathway serves the physiological purpose of increasing bone resorption to release calcium for breastmilk production postpartum but becomes maladaptive postmenopause, leading to osteoporosis. Finally, these results highlight the crosstalk between the brain-bone-breast-endocrine axis and the immune system during lactation.
哺乳期的牛奶生产对钙的需求很高,这些钙既可以通过母体骨吸收和饮食来满足。虽然已知乳腺来源的 PTHrP 在哺乳期驱动骨吸收,但产后雌激素丧失对骨骼的影响尚不清楚。我们使用病例对照研究设计来测试哺乳期小鼠雌激素丧失的影响。结果:在本研究中,我们首次表明,哺乳期雌激素丧失会激活记忆 T 细胞(T 细胞)产生 TNFα 和 IL-17A,以帮助骨吸收和钙释放。我们的研究揭示了产后从骨骼中释放钙的新机制。这些发现提供了几个新的见解。首先,免疫系统在后乳期的牛奶生产中起着关键作用。其次,从进化的角度来看,该途径的生理目的是增加骨吸收,以释放钙用于产后母乳生产,但在绝经后变得适应不良,导致骨质疏松症。最后,这些结果强调了哺乳期大脑-骨骼-乳腺内分泌轴与免疫系统之间的串扰。