Premium
Subcellular distribution of the insulin‐like growth factor (IGF) binding proteins (IGFBPs) 2 and 3 in articular chondrocytes
Author(s) -
Sun Tiezheng,
Hunziker Ernst B.,
Morales Teresa I.
Publication year - 2008
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.20660
Subject(s) - cytoplasm , microbiology and biotechnology , growth factor , chondrocyte , insulin like growth factor binding protein , insulin like growth factor , subcellular localization , cell fractionation , cartilage , biology , endocrinology , medicine , chemistry , receptor , biochemistry , anatomy , membrane
The insulin‐like growth factor (IGF) is a major anabolic regulator in articular cartilage. The IGF‐binding proteins (IGFBPs) are increased during osteoarthritis (OA), but the function of the later proteins remains unknown. In general, the IGFBPs are pluripotential effectors capable of IGF regulation and of acting on their own to control key cell functions, including survival and proliferation. The independent functions are often associated with their cell location, and therefore this study explores the distribution of IGFBP‐2 and IGFBP‐3 in articular chondrocytes. Immunohistochemistry was used to localize IGFBP‐2 in normal human articular cartilage. Bovine chondrocytes were used for subcellular fractionation (hypotonic cell lysis) under nonreducing conditions and nuclear purification (centrifugation on sucrose cushions). Cell fraction markers and IGFBPs were assayed in the subcellular fractions by Western immunoblot. The IHC results showed association of IGFBP‐2 with chondrocytes, but not with the nuclei. Subcellular fractionation of isolated chondrocytes yielded intact nuclei as assessed at the light microscopic level; the nuclear marker histone H1 was exclusively associated with this fraction. More than 90% of the cytoplasmic marker GAPDH and all the detectable IGFBP‐2 were in the cytoplasmic fraction. Immunoreactive IGFBP‐3 was found in the cytoplasmic and peri‐nuclear/nuclear fractions. Chondrocytes contain intracellular IGFBP‐2 and IGFBP‐3 but only IGFBP‐3 is associated with nuclei. This suggests the hypothesis that the actions of these IGFBPs in articular cartilage extend beyond the classic modulation of IGF receptor action. © 2008 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 26:1421–1427, 2008