Literature DB >> 21421796

Differential distribution of posttranslationally modified microtubules in osteoclasts.

Toshitaka Akisaka1, Hisaho Yoshida, Toshiya Takigawa.   

Abstract

The differential distribution of microtubules in osteoclasts in culture was examined by using antibodies against acetylated, tyrosinated, or detyrosinated tubulins. Tyrosinated tubulin was found throughout the cytoplasmic microtubules in all cells examined. An expanding protrusion that contained tyrosinated tubulin but none of the detyrosinated or acetylated form was seen in the immature osteoclasts. Detyrosinated or acetylated tubulin was detectable in the peripheral cytoplasm of the mature osteoclasts displaying the loss of the expanding protrusion. Although most of the microtubules were derived from the centrosome, noncentrosomal microtubules were distributed in the expanding protrusion, which was predominantly positive for tyrosinated tubulin. By tracing single microtubules, the authors found that their growing ends were always rich in tyrosinated tubulin subunits. End binding protein 1 bound preferentially to the microtubule ends. Both acetylated and tyrosinated microtubules were shown to be closely associated with podosomes. Microtubules appeared to grow over or into the podosomes; in addition, the growing ends of single microtubules could be observed to target the podosomes. Moreover, a microtubule-associated histone deacetylase 6 was localized in the podosomes of the osteoclast. On the basis of these results, the authors conclude that posttranslational modifications of microtubules may correlate with characteristic changes in podosome dynamics in osteoclasts.

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Year:  2011        PMID: 21421796      PMCID: PMC3201188          DOI: 10.1369/0022155411405334

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  49 in total

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9.  Macrophage podosomes assemble at the leading lamella by growth and fragmentation.

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3.  Microtubule dynamic instability controls podosome patterning in osteoclasts through EB1, cortactin, and Src.

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4.  Class II and IV HDACs function as inhibitors of osteoclast differentiation.

Authors:  Nicholas C Blixt; Bora K Faulkner; Kristina Astleford; Rosemary Lelich; Jacob Schering; Ekaterina Spencer; Rajaram Gopalakrishnan; Eric D Jensen; Kim C Mansky
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5.  Cytoplasmic hnRNPK interacts with GSK3β and is essential for the osteoclast differentiation.

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  5 in total

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