Department of Internal Medicine, Division of Infectious Diseases, University of Texas Medical Branch, Galveston, TX, United States.
Department of Orthopedic Surgery and Rehabilitation, The University of Texas Medical Branch, Galveston, TX, United States.
Front Immunol. 2022 Aug 2;13:846246. doi: 10.3389/fimmu.2022.846246. eCollection 2022.
Inflammation has a role in the pathogenesis of childhood malnutrition. We investigated the effect of malnutrition and inflammatory challenge on bone marrow composition and bone health. We studied an established murine model of moderate acute malnutrition at baseline and after acute inflammatory challenge with bacterial lipopolysaccharide (LPS), a surrogate of Gram-negative bacterial sepsis, or , the cause of visceral leishmaniasis. Both of these infections cause significant morbidity and mortality in malnourished children. Of the 2 stimuli, LPS caused more pronounced bone marrow changes that were amplified in malnourished mice. LPS challenge led to increased inflammatory cytokine expression (, , and ), inflammasome activation, and inflammatory monocyte accumulation in the bone marrow of malnourished mice. Depletion of inflammatory monocytes in -LysMcre-DT malnourished mice significantly reduced the inflammasome activation and IL1-ß production after LPS challenge. The inflammatory challenge also led to increased expansion of mesenchymal stem cells (MSCs), bone marrow adiposity, and expression of genes (, , and ) associated with adipogenesis in malnourished mice. This suggests that inflammatory challenge promotes differentiation of BM MSCs toward the adipocyte lineage rather than toward bone-forming osteoblasts in the malnourished host. Concurrent with this reduced osteoblastic potential there was an increase in bone-resorbing osteoclasts, enhanced osteoclast activity, upregulation of inflammatory genes, and IL-1B involved in osteoclast differentiation and activation. The resulting weakened bone formation and increased bone resorption would contribute to the bone fragility associated with malnutrition. Lastly, we evaluated the effect of replacing lipid rich in omega-6 fatty acids (corn oil) with lipid-rich in omega-3 fatty acids (fish oil) in the nutrient-deficient diet. LPS-challenged malnourished mice that received dietary fish oil showed decreased expression of inflammatory cytokines and and reduced osteoclast differentiation and activation in the bone marrow. This work demonstrates that the negative effect of inflammatory challenge on bone marrow is amplified in the malnourished host. Increasing dietary intake of omega-3 fatty acids may be a means to reduce inflammation and improve bone health in malnourished children.
炎症在儿童营养不良的发病机制中起作用。我们研究了营养不良和炎症挑战对骨髓组成和骨骼健康的影响。我们研究了一种已建立的中度急性营养不良的小鼠模型,在基线时以及在急性炎症挑战后进行研究,急性炎症挑战使用细菌脂多糖(LPS),革兰氏阴性菌败血症的替代物,或内脏利什曼病的原因。这两种感染都会导致营养不良儿童出现严重的发病率和死亡率。在这两种刺激物中,LPS 引起的骨髓变化更为明显,而在营养不良的小鼠中则更为明显。LPS 挑战导致营养不良小鼠骨髓中炎症细胞因子表达(、和)、炎性小体激活和炎症性单核细胞积累增加。在营养不良的 -LysMcre-DT 小鼠中耗尽炎性单核细胞后,LPS 挑战后炎性小体激活和 IL1-ß 产生显著减少。炎症挑战还导致间充质干细胞(MSCs)的扩张增加,骨髓脂肪过多,以及营养不良小鼠中与脂肪生成相关的基因(、和)的表达增加。这表明炎症挑战促进了骨髓间充质干细胞向脂肪细胞谱系的分化,而不是向营养不良宿主中的成骨细胞分化。随着这种成骨潜能的降低,破骨细胞的数量增加,破骨细胞活性增强,炎症基因上调,以及参与破骨细胞分化和激活的 IL-1B。由此产生的骨形成减弱和骨吸收增加将导致与营养不良相关的骨脆弱。最后,我们评估了在营养缺乏饮食中用富含ω-3 脂肪酸(鱼油)代替富含ω-6 脂肪酸(玉米油)对脂质的影响。接受富含鱼油的饮食的 LPS 挑战的营养不良小鼠表现出炎症细胞因子和的表达降低,以及骨髓中破骨细胞分化和激活减少。这项工作表明,炎症挑战对骨髓的负面影响在营养不良宿主中放大。增加ω-3 脂肪酸的饮食摄入可能是减少营养不良儿童炎症和改善骨骼健康的一种方法。