|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 107, Issue 2 589-600, Copyright © 1994 by Company of Biologists
JOURNAL ARTICLES |
CG Henderson, JB Tucker, MA Chaplin, JB Mackie, SN Maidment, MM Mogensen and CC Paton
School of Biological and Medical Sciences, University of St Andrews, Fife, Scotland.
Reorganization of centrosomal microtubule-organizing centres and the minus ends of microtubules occurs as the centrosomal ends of large microtubule bundles are repositioned and anchored to cell junctions in certain epithelial cells called inner pillar cells in the mouse organ of Corti. The microtubule bundle that assembles in each cell consists of two distinct microtubule arrays that run closely alongside each other. Both arrays are attached to the cell surface at their upper and lower ends. One of the arrays spans the entire length of a cell but the other is confined to its lower portion. Initially, about 3,000 microtubules elongate downwards from an apically situated centrosome in each cell. Subsequently, the minus ends of these microtubules, and the centrosome and its two centrioles, migrate for about 12 microns to the tip of a laterally directed projection. Then, a meshwork of dense material accumulates to link microtubule minus ends and the centrosome to cell junctions at the tip of the projection. Pericentriolar satellite bodies, which form after the initial burst of microtubule nucleation, may represent a condensed and inactive concentration of microtubule-nucleating elements. Surprisingly, as a cell matures, about 2,000 microtubules are eliminated from the centrosomal end of the microtubule bundle. However, about 2,000 microtubules are added to the basal portion of each bundle at levels that are remote with respect to the location of the centrosome. Possibly, these microtubules have escaped from the centrosome. If this is the case, then both the plus and minus ends of most of the errant microtubules are captured by sites at the cell surface where the ends are finally anchored. Alternatively, each cell possesses at least one other major microtubule-nucleating site (which does not possess centrioles) in addition to its centrosome.
This article has been cited by other articles:
![]() |
M. E. Grespin, G. M. C. Bonamy, V. R. Roggero, N. G. Cameron, L. E. Adam, A. P. Atchison, V. M. Fratto, and L. A. Allison Thyroid Hormone Receptor {alpha}1 Follows a Cooperative CRM1/Calreticulin-mediated Nuclear Export Pathway J. Biol. Chem., September 12, 2008; 283(37): 25576 - 25588. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Goicoechea, M. A. Pallero, P. Eggleton, M. Michalak, and J. E. Murphy-Ullrich The Anti-adhesive Activity of Thrombospondin Is Mediated by the N-terminal Domain of Cell Surface Calreticulin J. Biol. Chem., September 27, 2002; 277(40): 37219 - 37228. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Tran, R. Pankov, S. D. Tran, B. Hampton, W. H. Burgess, and K. M. Yamada Integrin clustering induces kinectin accumulation J. Cell Sci., May 15, 2002; 115(10): 2031 - 2040. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Seddiki, F. Nato, P. Lafaye, Z. Amoura, J. C. Piette, and J. C. Mazie Calreticulin, a Potential Cell Surface Receptor Involved in Cell Penetration of Anti-DNA Antibodies J. Immunol., May 15, 2001; 166(10): 6423 - 6429. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Kwon, C. S. Park, K.-r. Choi, C.-S. Park, J. Ahnn, J. I. Kim, S. H. Eom, S. J. Kaufman, and W. K. Song Calreticulin Couples Calcium Release and Calcium Influx in Integrin-mediated Calcium Signaling Mol. Biol. Cell, April 1, 2000; 11(4): 1433 - 1443. [Abstract] [Full Text] |
||||
![]() |
S Liu, D. Calderwood, and M. Ginsberg Integrin cytoplasmic domain-binding proteins J. Cell Sci., January 10, 2000; 113(20): 3563 - 3571. [Abstract] [PDF] |
||||
![]() |
M. Mogensen, A Malik, M Piel, V Bouckson-Castaing, and M Bornens Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein J. Cell Sci., January 9, 2000; 113(17): 3013 - 3023. [Abstract] [PDF] |
||||
![]() |
G. J. Mizejewski Role of Integrins in Cancer: Survey of Expression Patterns Experimental Biology and Medicine, November 1, 1999; 222(2): 124 - 138. [Abstract] [Full Text] |
||||
![]() |
J. M. Patel, Y. D. Li, J. Zhang, C. H. Gelband, M. K. Raizada, and E. R. Block Increased expression of calreticulin is linked to ANG IV-mediated activation of lung endothelial NOS Am J Physiol Lung Cell Mol Physiol, October 1, 1999; 277(4): L794 - L801. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Zhu and Z. Wang Calreticulin Expression Is Associated with Androgen Regulation of the Sensitivity to Calcium Ionophore-induced Apoptosis in LNCaP Prostate Cancer Cells Cancer Res., April 1, 1999; 59(8): 1896 - 1902. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Rodionov, E. Nadezhdina, and G. Borisy Centrosomal control of microtubule dynamics PNAS, January 5, 1999; 96(1): 115 - 120. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Zhu, E. B. Pewitt, X. Cai, E. B. Cohn, S. Lang, R. Chen, and Z. Wang Calreticulin: An Intracellular Ca++-Binding Protein Abundantly Expressed and Regulated by Androgen in Prostatic Epithelial Cells Endocrinology, October 1, 1998; 139(10): 4337 - 4344. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. E. Aplin, A. Howe, S. K. Alahari, and R. L. Juliano Signal Transduction and Signal Modulation by Cell Adhesion Receptors: The Role of Integrins, Cadherins, Immunoglobulin-Cell Adhesion Molecules, and Selectins Pharmacol. Rev., June 1, 1998; 50(2): 197 - 264. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Dai, M. Stewart, B. Ritchie, N. Mesaeli, S. Raha, D. Kolodziejczyk, M. L. Hobman, L. Y. Liu, W. Etches, N. Nation, et al. Calreticulin, a Potential Vascular Regulatory Protein, Reduces Intimal Hyperplasia After Arterial Injury Arterioscler. Thromb. Vasc. Biol., November 1, 1997; 17(11): 2359 - 2368. [Abstract] [Full Text] |
||||
![]() |
G. M. Denning, K. G. Leidal, V. A. Holst, S. S. Iyer, D. W. Pearson, J. R. Clark, W. M. Nauseef, and R. A. Clark Calreticulin Biosynthesis and Processing in Human Myeloid Cells: Demonstration of Signal Peptide Cleavage and N-Glycosylation Blood, July 1, 1997; 90(1): 372 - 381. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. J. Keating, J. G. Peloquin, V. I. Rodionov, D. Momcilovic, and G. G. Borisy Microtubule release from the centrosome PNAS, May 13, 1997; 94(10): 5078 - 5083. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Seki, N. Koyama, N. L. Kovach, T. Yednock, A. W. Clowes, and J. M. Harlan Regulation of ß1-Integrin Function in Cultured Human Vascular Smooth Muscle Cells Circ. Res., April 1, 1996; 78(4): 596 - 605. [Abstract] [Full Text] |
||||
![]() |
J. Tucker, M. Mogensen, C. Paton, J. Mackie, C. Henderson, and L. Leckie Formation of two microtubule-nucleating sites which perform differently during centrosomal reorganization in a mouse cochlear epithelial cell J. Cell Sci., January 4, 1995; 108(4): 1333 - 1345. [Abstract] [PDF] |
||||
![]() |
C. Henderson, J. Tucker, M. Mogensen, J. Mackie, M. Chaplin, N. Slepecky, and L. Leckie Three microtubule-organizing centres collaborate in a mouse cochlear epithelial cell during supracellularly coordinated control of microtubule positioning J. Cell Sci., January 1, 1995; 108(1): 37 - 50. [Abstract] [PDF] |
||||