Visualization of structural organization of ventral membranes of sheared-open resorbing osteoclasts attached to apatite pellets

• Published in: Cell and tissue research Vol. 360; no. 2; pp. 347 - 362
• Main Authors: Akisaka, Toshitaka, Yoshida, Atsushi
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer-Verlag 01.05.2015; Springer Berlin Heidelberg; Springer; Springer Nature B.V
• Subjects: actin; Actin Cytoskeleton - metabolism; Actins - metabolism; Animals; apatite; Apatites - chemistry; Biomedical and Life Sciences; Biomedicine; Cell Adhesion; Cell adhesion & migration; Cell Membrane Structures - metabolism; Cell Membrane Structures - ultrastructure; Cells, Cultured; clathrin; Clathrin - metabolism; Endocytosis; glass; Halides; Human Genetics; Membranes; microfilaments; Molecular Medicine; Muscle proteins; Myosin; Myosin Subfragments - metabolism; osteoclasts; Osteoclasts - metabolism; Osteoclasts - ultrastructure; particles; pellets; Phosphate minerals; Proteins; Proteomics; pseudopodia; Rabbits; Regular Article; resorption; Actin polarity; Resorbing osteoclasts; Membrane modification; Podosome; Clathrin sheets
• ISSN: 0302-766X; 1432-0878
• DOI: 10.1007/s00441-014-2085-4

Osteoclasts are highly polarized cells from both morphological and functional points of view. Using quick-freeze, rotary-replication methods combined with cell-shearing, we clarified the variability of cytoplasmic surface of the polarized membranes of osteoclasts seeded on apatite. As to the organization of actin filaments and clathrin sheets, we confirmed almost the same ventral membrane specializations of osteoclasts on apatite as seen on glass plates. The organized actin filaments and membrane-associated particles supported the ruffled border membranes. Inside the actin sealing zone, membrane specializations were not always occupied with the ruffled border but also with other types of membranes. Some osteoclasts formed an actin ring but lacked the ruffled border projections. We report a unique and distinctive membrane modification of apatite-attached osteoclasts, i.e., the presence of dense aggregates of membrane-associated particles and related structures not found in the osteoclasts seeded on glass plates. Actin filament polarity in the podosomes was determined by decoration with myosin S1. The actin filament polarity within podosome appears to be oriented predominantly with its barbed ends toward the core, whereas the interconnecting F-actin appears to be mixed oriented. Two different types of clathrin plaques displayed different distributions: clathrin-dependent endocytosis was observed in the ruffled border regions, whereas flat clathrin sheets were found in the leading edge of lamellipodia and near podosomes. The clathrin sheets adhered to the apatite surface tightly on the ventral membranes overlaying the resorption lacunae. All these membrane specializations as mentioned above may indicate the functional variability of osteoclasts seeded on apatite.