Fibrotic alterations in human annulus fibrosus correlate with progression of intervertebral disc herniation

• Type: Article in International Scientific Journal
• Date: 2022

Authors

Castro, AL (Author) Other; Ribeiro Machado, C (Author) Other; Oliveira, CM (Author) Other; Teixeira, GQ (Author) Other; Neidlinger Wilke, C (Author) Other; Paulo Pereira (Author) FMUP; Vaz, R (Author) Other; Barbosa, MA (Author) Other; Goncalves, RM (Author) Other

Journal

The Journal is awaiting validation by the Administrative Services.

Title: ARTHRITIS RESEARCH & THERAPY

Vol. 24

ISSN: 1478-6354

Indexing

ISI Web of Knowledge - 13 Citations

Scopus - 12 Citations

Other information

Authenticus ID: P-00V-ZX4

DOI: 10.1186/s13075-021-02690-w

Abstract (EN): Background Intervertebral disc (IVD) herniation is characterized by annulus fibrosus failure (AF) in containing the nucleus pulposus (NP). IVD herniation involves cellular and extracellular matrix (ECM) alterations that have been associated with tissue fibrosis, although still poorly investigated. Methods Here, fibrotic alterations in human AF were evaluated, by characterizing the herniated ECM. Human AF samples (herniated lumbar IVD (n = 39, age 24-83) and scoliosis controls (n = 6, age 15-21)) were processed for transmission electron microscopy and histological/immunohistochemical analysis of fibrotic markers. Correlations between the fibrotic markers in AF ECM and the degree of NP containment (protused, contained and uncontained) and patients' age were conducted. Results Our results demonstrate that with herniation progression, i.e. loss of NP containment, human AF presents less stained area of sulphated glycosaminoglycans and collagen I, being collagen I fibres thinner and disorganized. On the other hand, fibronectin stained area and percentage of alpha-smooth muscle actin+ cells increase in human AF, while matrix metalloproteinase-12 (MMP12) production and percentage of macrophages (CD68+ cells) remain constant. These structural and biochemical fibrotic alterations observed in human AF with herniation progression occur independently of the age. Conclusions The characterization of human AF here conducted evidence the presence of fibrosis in degenerated IVD, while highlighting the importance of considering the herniation progression stage, despite the patients' age, for a better understanding of the mechanisms behind AF failure and IVD herniation.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 14