微生物诱导的骨基质强度增减可在骨骼成熟后开始。

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2024-10-29 DOI:10.1093/jbmr/zjae157
Chongshan Liu, Erika L Cyphert, Samuel J Stephen, Bowen Wang, Angie L Morales, Jacob C Nixon, Nicholas R Natsoulas, Matthew Garcia, Pablo Blazquez Carmona, Albert C Vill, Eve Donnelly, Ilana L Brito, Deepak Vashishth, Christopher J Hernandez
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引用次数: 0

摘要

最近对小鼠的研究表明,肠道微生物群可以调节骨组织强度。然而,之前的研究涉及对生长期动物肠道微生物组的改变,目前还不清楚在生命后期应用同样的微生物组改变是否会改变基质强度。在此,我们使用口服抗生素(氨苄青霉素+新霉素)在骨骼成熟(16 周龄)之前和/或之后改变了肠道微生物组的组成。雄性和雌性小鼠(共 143 只,每组/性别 12-17 只)被分配到五个研究组:1)未改变组;2)连续组(4-24 周龄给药);3)延迟组(16-24 周龄才给药);4)初始组(4-16 周龄给药,16 周龄暂停);5)重组组(从 4-16 周龄开始给药,然后从未曾改变的供体进行粪便微生物群移植)。动物在 24 周龄时安乐死。与未改变组相比,连续组(P=.001)、延迟组(P=.005)和初始组(P=.040)的雄性小鼠股骨的骨基质强度比预期的几何值低 25-35%。恢复肠道微生物群后,骨基质强度与未改变动物相似(P=.929)。在雌性动物中,微生物诱导的骨基质强度变化趋势与雄性动物相同,但没有显著差异,这表明骨基质对肠道微生物群的反应取决于性别。拉曼光谱观察到骨基质的化学成分略有不同。我们的研究结果表明,微生物诱导的男性骨基质损伤可在骨骼成熟后开始和/或逆转。骨骼成熟(16 周)后形成的股骨皮质骨的比例很小;这表明微生物诱导的骨基质变化是通过一种尚未确定的机制在没有成骨细胞/破骨细胞更替的情况下发生的。这些发现提供了证据,证明骨基质的机械特性可在成人骨骼中发生改变。
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Microbiome-induced increases and decreases in bone matrix strength can be initiated after skeletal maturity.

Recent studies in mice have indicated that the gut microbiome can regulate bone tissue strength. However, prior work involved modifications to the gut microbiome in growing animals and it is unclear if the same changes in the microbiome, applied later in life, would change matrix strength. Here we changed the composition of the gut microbiome before and/or after skeletal maturity (16 weeks of age) using oral antibiotics (ampicillin + neomycin). Male and female mice (n = 143 total, n = 12-17/group/sex) were allocated into five study groups: (1) Unaltered, (2) Continuous (dosing 4-24 weeks of age), (3) Delayed (dosing only 16-24 weeks of age), (4) Initial (dosing 4-16 weeks of age, suspended at 16 weeks), and (5) Reconstituted (dosing from 4-16 weeks following by fecal microbiota transplant from Unaltered donors). Animals were euthanized at 24 weeks of age. In males, bone matrix strength in the femur was 25%-35% less than expected by geometry in mice from the Continuous (p = 0.001), Delayed (p = 0.005), and Initial (p = 0.040) groups as compared to Unaltered. Reconstitution of the gut microbiota led to a bone matrix strength similar to Unaltered animals (p = 0.929). In females, microbiome-induced changes in bone matrix strength followed the same trend as males but were not significantly different, demonstrating a sex-dependent response of bone matrix to the gut microbiota. Minor differences in chemical composition of bone matrix were observed with Raman spectroscopy. Our findings indicate that microbiome-induced impairment of bone matrix in males can be initiated and/or reversed after skeletal maturity. The portion of the femoral cortical bone formed after skeletal maturity (16 weeks) was small; suggesting that microbiome-induced changes in bone matrix occurred without osteoblast/osteoclast turnover through a yet unidentified mechanism. These findings provide evidence that the mechanical properties of bone matrix can be altered in the adult skeleton.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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