Bacterial Lipopolysaccharides Exacerbate Neurogenic Heterotopic Ossification Development

Author:

Salga Marjorie123,Samuel Selwin G14,Tseng Hsu‐Wen1,Gatin Laure235,Girard Dorothée6,Rival Bastien6,Barbier Valérie1,Bisht Kavita1,Shatunova Svetlana1,Debaud Charlotte2,Winkler Ingrid G1,Paquereau Julie3,Dinh Aurélien7,Genêt Guillaume2,Kerever Sébastien8,Abback Paer‐Sélim9,Banzet Sébastien6,Genêt François23,Lévesque Jean‐Pierre1,Alexander Kylie A1ORCID

Affiliation:

1. Mater Research Institute—The University of Queensland Translational Research Institute Woolloongabba Australia

2. University of Versailles Saint Quentin en Yvelines END:ICAP U1179 INSERM, UFR Simone Veil‐Santé Montigny le Bretonneux France

3. UPOH (Unité Péri Opératoire du Handicap), Physical and Rehabilitation Medicine Department Raymond‐Poincaré Hospital, Assistance Publique‐Hôpitaux de Paris (AP‐HP) Garches France

4. Department of Oral Pathology and Microbiology Saveetha Dental College and Hospitals Chennai India

5. Department of Orthopedic Surgery Raymond Poincaré Hospital, AP‐HP Garches France

6. Institut de Recherche Biomédicale des Armées (IRBA) INSERM UMR‐MD 1197 Clamart France

7. Department of Infectious Diseases Raymond Poincaré Hospital, AP‐HP Garches France

8. Department of Anesthesiology and Critical Care Lariboisière University Hospital, AP‐HP Paris France

9. Department of Anesthesiology and Critical Care Beaujon Hospital, DMU Parabol, AP‐HP Clichy France

Abstract

ABSTRACTNeurogenic heterotopic ossifications (NHO) are heterotopic bones that develop in periarticular muscles after severe central nervous system (CNS) injuries. Several retrospective studies have shown that NHO prevalence is higher in patients who suffer concomitant infections. However, it is unclear whether these infections directly contribute to NHO development or reflect the immunodepression observed in patients with CNS injury. Using our mouse model of NHO induced by spinal cord injury (SCI) between vertebrae T11 to T13, we demonstrate that lipopolysaccharides (LPS) from gram‐negative bacteria exacerbate NHO development in a toll‐like receptor‐4 (TLR4)‐dependent manner, signaling through the TIR‐domain‐containing adapter‐inducing interferon‐β (TRIF/TICAM1) adaptor rather than the myeloid differentiation primary response‐88 (MYD88) adaptor. We find that T11 to T13 SCI did not significantly alter intestinal integrity nor cause intestinal bacteria translocation or endotoxemia, suggesting that NHO development is not driven by endotoxins from the gut in this model of SCI‐induced NHO. Relevant to the human pathology, LPS increased expression of osteoblast markers in cultures of human fibro‐adipogenic progenitors isolated from muscles surrounding NHO biopsies. In a case–control retrospective study in patients with traumatic brain injuries, infections with gram‐negative Pseudomonas species were significantly associated with NHO development. Together these data suggest a functional association between gram‐negative bacterial infections and NHO development and highlights infection management as a key consideration to avoid NHO development in patients. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Funder

Mater Foundation

National Health and Medical Research Council

U.S. Department of Defense

University of Queensland

Publisher

Oxford University Press (OUP)

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference83 articles.

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