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      Diversity of actin architecture in human osteoclasts: network of curved and branched actin supporting cell shape and intercellular micrometer-level tubes

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          Abstract

          Osteoclasts are multinucleated bone-resorbing cells with a dynamic actin cytoskeleton. Osteoclasts are derived from circulating mononuclear precursors. Confocal and stimulated emission depletion (STED) super-resolution microscopy was used to investigate peripheral blood-derived human osteoclasts cultured on glass surfaces. STED and confocal microscopy demonstrated that the actin was curved and branched, for instance, in the vicinity of membrane ruffles. The overall architecture of the curved actin network extended from the podosomes to the top of the cell. The other novel finding was that a micrometer-level tube containing actin bridged the osteoclasts well above the level of the culture glass. The actin filaments of the tubes originated from the network of curved actin often surrounding a group of nuclei. Furthermore, nuclei were occasionally located inside the tubes. Our findings demonstrated the accumulation of c-Src, cortactin, cofilin, and actin around nuclei suggesting their role in nuclear processes such as the locomotion of nuclei. ARP2/3 labeling was abundant at the substratum level of osteoclasts and in the branched actin network, where it localized to the branching points. We speculate that the actin-containing tubes of osteoclasts may provide a means of transportation of nuclei, e.g., during the fusion of osteoclasts. These novel findings can pave the way for future studies aiming at the elucidation of the differentiation of multinucleated osteoclasts.

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          The online version of this article (doi:10.1007/s11010-017-3004-2) contains supplementary material, which is available to authorized users.

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          The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene.

          Mice homozygous for the recessive mutation osteopetrosis (op) on chromosome 3 have a restricted capacity for bone remodelling, and are severely deficient in mature macrophages and osteoclasts. Both cell populations originate from a common haemopoietic progenitor. As op/op mice are not cured by transplants of normal bone marrow cells, the defects in op/op mice may be associated with an abnormal haematopoietic microenvironment rather than with an intrinsic defect in haematopoietic progenitors. To investigate the molecular and biochemical basis of the defects caused by the op mutation, we established primary fibroblast cell lines from op/op mice and tested the ability of these cell lines to support the proliferation of macrophage progenitors. We show that op/op fibroblasts are defective in production of functional macrophage colony-stimulating factor (M-CSF), although its messenger RNA (Csfm mRNA) is present at normal levels. This defect in M-CSF production and the recent mapping of the Csfm structural gene near op on chromosome 3 suggest that op is a mutation within the Csfm gene itself. We have sequenced Csfm complementary DNA prepared from op/op fibroblasts and found a single base pair insertion in the coding region of the Csfm gene that generates a stop codon 21 base pairs downstream. Thus, the op mutation is within the Csfm coding region and we conclude that the pathological changes in this mutant result from the absence of M-CSF.
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            The tension mounts: Stress fibers as force-generating mechanotransducers

            Stress fibers (SFs) are often the most prominent cytoskeletal structures in cells growing in tissue culture. Composed of actin filaments, myosin II, and many other proteins, SFs are force-generating and tension-bearing structures that respond to the surrounding physical environment. New work is shedding light on the mechanosensitive properties of SFs, including that these structures can respond to mechanical tension by rapid reinforcement and that there are mechanisms to repair strain-induced damage. Although SFs are superficially similar in organization to the sarcomeres of striated muscle, there are intriguing differences in their organization and behavior, indicating that much still needs to be learned about these structures.
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              Reversible stress softening of actin networks.

              The mechanical properties of cells play an essential role in numerous physiological processes. Organized networks of semiflexible actin filaments determine cell stiffness and transmit force during mechanotransduction, cytokinesis, cell motility and other cellular shape changes. Although numerous actin-binding proteins have been identified that organize networks, the mechanical properties of actin networks with physiological architectures and concentrations have been difficult to measure quantitatively. Studies of mechanical properties in vitro have found that crosslinked networks of actin filaments formed in solution exhibit stress stiffening arising from the entropic elasticity of individual filaments or crosslinkers resisting extension. Here we report reversible stress-softening behaviour in actin networks reconstituted in vitro that suggests a critical role for filaments resisting compression. Using a modified atomic force microscope to probe dendritic actin networks (like those formed in the lamellipodia of motile cells), we observe stress stiffening followed by a regime of reversible stress softening at higher loads. This softening behaviour can be explained by elastic buckling of individual filaments under compression that avoids catastrophic fracture of the network. The observation of both stress stiffening and softening suggests a complex interplay between entropic and enthalpic elasticity in determining the mechanical properties of actin networks.
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                Author and article information

                Contributors
                juhpel@utu.fi
                Journal
                Mol Cell Biochem
                Mol. Cell. Biochem
                Molecular and Cellular Biochemistry
                Springer US (New York )
                0300-8177
                1573-4919
                14 March 2017
                14 March 2017
                2017
                : 432
                : 1
                : 131-139
                Affiliations
                [1 ]ISNI 0000 0001 2097 1371, GRID grid.1374.1, Department of Cell Biology and Anatomy, Institute of Biomedicine, , University of Turku, ; Kiinamyllynkatu 10, 20520 Turku, Finland
                [2 ]ISNI 0000 0001 2097 1371, GRID grid.1374.1, Laboratory of Biophysics, Department of Cell Biology and Anatomy and Medicity Research Laboratories, , University of Turku, ; P.O. Box 123, 20521 Turku, Finland
                [3 ]ISNI 0000 0004 1937 0626, GRID grid.4714.6, Division of Pathology, Department of Laboratory Medicine, , Karolinska Institutet, ; Stockholm, Sweden
                [4 ]ISNI 0000 0001 2097 1371, GRID grid.1374.1, Department of Dermatology, , University of Turku and Turku University Hospital, ; PO BOX 52, 20521 Turku, Finland
                Author information
                http://orcid.org/0000-0002-5880-9924
                Article
                3004
                10.1007/s11010-017-3004-2
                5532409
                28293874
                2aac05eb-fc00-4654-b7b5-f1483fc7adba
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 22 December 2016
                : 4 March 2017
                Funding
                Funded by: The Academy of Finland
                Award ID: 127080
                Award Recipient :
                Funded by: The Jalmari and Rauha Ahokas Foundation
                Categories
                Article
                Custom metadata
                © Springer Science+Business Media, LLC 2017

                Biochemistry
                osteoclasts,branched actin,curved actin,micrometer-level tubes,mlt,tunneling nanotubes,tnt,sted microscopy,nuclear transport

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