# Spinal hypermobility accelerates ossification in posterior longitudinal ligaments: insights from an in vivo mouse model

## TL;DR

This study shows that increased spinal movement in mice accelerates abnormal bone growth in spine ligaments, offering new insights into a condition called OPLL.

## Contribution

The study is the first to demonstrate in vivo that spinal hypermobility promotes ligament ossification in a mouse model of OPLL.

## Key findings

- Spinal hypermobility increased ligament ossification and chondrocyte proliferation in mice.
- Fast hypermobility reduced spinal range of motion and motor function scores compared to controls.
- Key proteins like SP7, RUNX2, and OCN were upregulated in hypermobility-induced ossification.

## Abstract

Ossification of the posterior longitudinal ligaments (OPLL) is characterized by heterotopic ossification in the posterior longitudinal ligament of spine. Our earlier research found that mechanical stimulation enhances osteogenic differentiation in OPLL-derived ligament cells. Nevertheless, the function of hypermobility of the spine on ligament ossification remain unexplored in vivo.

We created the novel stimulation device to induce spinal hypermobility in mice with heterotopic ossification of the spine ligaments. The mice were randomly divided into three groups, control, slow hypermobility (SH) group and fast hypermobility (FH) group according to the frequency of spinal movement. Ligament ossification and changes in spinal range of motion (ROM) were assessed using micro-CT and X-rays. Morphological alterations were examined through HE staining. Behavioral evaluation was performed using the Basso Mouse Scale (BMS) score and inclined plane test (IPT). Immunofluorescence was employed to examine the expression of related proteins.

After 8 weeks, it showed increased ligament ossification and chondrocyte proliferation both in SH and FH group. After 16 weeks, The BMS score and IPT were lower both in the SH and FH group compared to the controls. Additionally, the ROM of cervicothoracic and thoracolumbar spine was lower in the FH group than in the controls. Immunofluorescence analysis revealed increased levels of SP7, RUNX2, OCN, DLX5, NOTCH1, and HES1 in the ligament tissues of the FH group compared to controls.

spinal hypermobility promotes the progression of ossification in mice with heterotopic ossification of the spine, shedding new light on the pathogenesis of OPLL.