Abstract

Hematopoiesis and bone interact in various developmental and pathological processes. Neurogenic heterotopic ossifications (NHO) are the formation of ectopic hematopoietic bones in peri-articular muscles that develop following severe lesions of the central nervous system such as traumatic cerebral or spinal injuries or strokes. This review will focus on the hematopoietic facet of NHO. The characterization of NHO demonstrates the presence of hematopoietic marrow in which quiescent hematopoietic stem cells (HSC) are maintained by a functional stromal microenvironment, thus documenting that NHOs are neo-formed ectopic HSC niches. Similarly to adult bone marrow, the NHO permissive environment supports HSC maintenance, proliferation and differentiation through bidirectional signaling with mesenchymal stromal cells and endothelial cells, involving cell adhesion molecules, membrane-bound growth factors, hormones, and secreted matrix proteins. The participation of the nervous system, macrophages and inflammatory cytokines including oncostatin M and transforming growth factor (TGF)-β in this process, reveals how neural circuitry fine-tunes the inflammatory response to generate hematopoietic bones in injured muscles. The localization of NHOs in the peri-articular muscle environment also suggests a role of muscle mesenchymal cells and bone metabolism in development of hematopoiesis in adults. Little is known about the establishment of bone marrow niches and the regulation of HSC cycling during fetal development. Similarities between NHO and development of fetal bones make NHOs an interesting model to study the establishment of bone marrow hematopoiesis during development. Conversely, identification of stage-specific factors that specify HSC developmental state during fetal bone development will give more mechanistic insights into NHO.

Highlights

  • Heterotopic ossification (HO) is an abnormal development of bone tissue within soft tissue

  • In lineage-tracing experiments in which either satellite cells (SCs) or fibro-adipogenic progenitors (FAPs) are labeled, we find that following spinal cord injuries (SCI), Neurogenic heterotopic ossifications (NHO) are derived from Prrx1 expressing FAPs, not from Pax7 expressing SCs (Tseng et al, 2019)

  • The close relationship between central nervous system (CNS), SNS, Parasympathetic Nervous System, bone metabolism and hematopoietic stem cells (HSC) migration, differentiation and self-renewal is illustrated by the important role of the circadian norepinephrine release by SNS nerves which triggers β3 adrenergic receptors (AR) and β2 AR expressed by BM mesenchymal cells and osteoblasts in both humans and mice (Golan et al, 2018, 2019)

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Summary

Introduction

Heterotopic ossification (HO) is an abnormal development of bone tissue within soft tissue. The local or systemic production of inflammatory mediators that stimulate the recruitment of MSCs, endothelial progenitors or other stem cells from the bone marrow and alter tissue repair have been proposed to provide a microenvironment/matrix supporting mineralization (Wang et al, 2004; Davis et al, 2013).

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