Open AccessAn in vitro 3D annulus fibrosus cell culture model with type I collagen: An examination of cell–matrix interactions
Author(s) -
Molladavoodi Sara,
DeWitteOrr Stephanie J.,
Gregory Diane E.
Publication year - 2022
Publication title -
jor spine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
0ISSN - 2572-1143
DOI - 10.1002/jsp2.1193
Subject(s) - extracellular matrix , in vitro , contraction (grammar) , microbiology and biotechnology , intervertebral disc , chemistry , matrix (chemical analysis) , lipopolysaccharide , type i collagen , annulus (botany) , cell culture , biophysics , anatomy , immunology , pathology , biology , medicine , biochemistry , genetics , chromatography , botany
Background Disorders of the intervertebral disc (IVD) are widely known to result in low back pain; one of the most common debilitating conditions worldwide. As a multifaceted condition, both inflammatory environment and mechanical factors can play a crucial role in IVD damage, and in particular, in the annulus fibrosus (AF), the highly collagenous outer ring of the IVD. As a result, a better understanding of how cells from the IVD, and specifically the AF, interact and respond to their environment is imperative. Goal The goal of this study is to use collagen type I as an in vitro three‐dimensional extracellular matrix for AF cells of IVD and briefly examine both the cellular and mechanical effect of exposure to an inflammatory stimulant. Methods We utilized type I collagen as a 3D in vitro model material for culturing AF cells of Sprague Dawley rat tail IVDs. Results We showed that the cultured cells are viable and metabolically active; these cells also induced a distinct and significant contraction on their collagen matrix. Furthermore, to demonstrate potential versatility of our model our model and its versatility, we used lipopolysaccharide (LPS), as a known inflammatory stimulant in IVDs, to manipulate the cells and their interaction. LPS treatment resulted in detectable changes to the contraction cells induced on the collagen matrix and affected the mechanical properties of these constructs.