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ORIGINAL RESEARCH article

Front. Cell. Infect. Microbiol.

Sec. Intestinal Microbiome

Volume 15 - 2025 | doi: 10.3389/fcimb.2025.1535666

This article is part of the Research Topic Fecal Microbiota Transplants: challenges in translating microbiome research to clinical applications View all 19 articles

Fecal microbiota transplantation alleviates lipopolysaccharide-induced osteoporosis by modulating gut microbiota and long non-coding RNA TUG1 expression

Provisionally accepted
Pengcheng Ma Pengcheng Ma 1Ruoyi Wang Ruoyi Wang 1Huizhi Chen Huizhi Chen 1Jiachun Zheng Jiachun Zheng 1Weijie Yang Weijie Yang 1Bo Meng Bo Meng 1Yifan Liu Yifan Liu 1Yao Lu Yao Lu 2Jing Zhao Jing Zhao 2*Hongwei Gao Hongwei Gao 1,3*
  • 1 Shandong Public Health Clinical Center, Jinan, China
  • 2 Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life science, Shandong University, Qingdao, Shandong Province, China
  • 3 School of Mechanical Engineering, Shandong University, Jinan, Shandong Province, China

The final, formatted version of the article will be published soon.

    To study whether fecal microbiota transplantation (FMT) can alleviate lipopolysaccharide (LPS)-induced osteoporosis (OP) by regulating the composition and abundance of gut microbiota and the expression level of long non-coding RNA (lncRNA) TUG1.Methods Twenty C57BL/6 mice were selected. Two mice were randomly designated as fecal donors, while the remaining mice were randomly divided into control group, LPS group, and LPS + FMT group. Each group consisted of 6 mice. The mice in the LPS and LPS + FMT groups were intraperitoneally (qRT-PCR) was used to compare the expression levels of lncRNA TUG1 in the intestines and serum of mice in the 3 groups.Results Micro-CT showed that compared with the control group, the mice in the LPS group had more bone loss. The bone mineral density, trabecular number, and trabecular thickness of the control group was higher, and the trabecular separation was smaller. The models were validated effectively. HE staining showed that compared with the control group, the bone trabeculae in the LPS group were thinner and sparse, while that in the LPS + FMT group were dense and clear. The 16s rRNA sequencing showed that the abundance of Bacteroides and Lactobacillus in LPS+FMT group was significantly higher than that in LPS group. Immunofluorescence staining showed that the RUNX2 level in the control group and LPS + FMT group was similar, and both were higher than that in the LPS group. The qRT-PCR results showed that the TUG1 mRNA level in the control group and LPS + FMT group was similar and significantly higher than that in the LPS group.FMT can enhance osteoblast levels and improve bone structure by modulating the abundance of gut microbiota in OP mice (such as increasing Bacteroides and Lactobacillus populations) and promoting the expression of lncRNA TUG1, thereby alleviating LPS-induced OP.

    Keywords: fecal microbiota transplantation, Osteoporosis, Gut Microbiota, lncRNA, Lipopolysaccharides

    Received: 14 Jan 2025; Accepted: 28 Mar 2025.

    Copyright: © 2025 Ma, Wang, Chen, Zheng, Yang, Meng, Liu, Lu, Zhao and Gao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Jing Zhao, Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life science, Shandong University, Qingdao, Shandong Province, China
    Hongwei Gao, Shandong Public Health Clinical Center, Jinan, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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