| Literature DB >> 28935572 |
Takeyuki Saito1, Masamitsu Hara1, Hiromi Kumamaru2, Kazu Kobayakawa2, Kazuya Yokota3, Ken Kijima1, Shingo Yoshizaki1, Katsumi Harimaya2, Yoshihiro Matsumoto2, Kenichi Kawaguchi2, Mitsumasa Hayashida2, Yutaka Inagaki4, Keiichiro Shiba3, Yasuharu Nakashima2, Seiji Okada5.
Abstract
Ligamentum flavum (LF) hypertrophy causes lumbar spinal canal stenosis, leading to leg pain and disability in activities of daily living in elderly individuals. Although previous studies have been performed on LF hypertrophy, its pathomechanisms have not been fully elucidated. In this study, we demonstrated that infiltrating macrophages were a causative factor for LF hypertrophy. Induction of macrophages into the mouse LF by applying a microinjury resulted in LF hypertrophy along with collagen accumulation and fibroblasts proliferation at the injured site, which were very similar to the characteristics observed in the severely hypertrophied LF of human. However, we found that macrophage depletion by injecting clodronate-containing liposomes counteracted LF hypertrophy even with microinjury. For identification of fibroblasts in the LF, we used collagen type I α2 linked to green fluorescent protein transgenic mice and selectively isolated green fluorescent protein-positive fibroblasts from the microinjured LF using laser microdissection. A quantitative RT-PCR on laser microdissection samples revealed that the gene expression of collagen markedly increased in the fibroblasts at the injured site with infiltrating macrophages compared with the uninjured location. These results suggested that macrophage infiltration was crucial for LF hypertrophy by stimulating collagen production in fibroblasts, providing better understanding of the pathophysiology of LF hypertrophy.Entities:
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Year: 2017 PMID: 28935572 DOI: 10.1016/j.ajpath.2017.08.020
Source DB: PubMed Journal: Am J Pathol ISSN: 0002-9440 Impact factor: 4.307