» Articles » PMID: 10444072

Insoluble Gamma-tubulin-containing Structures Are Anchored to the Apical Network of Intermediate Filaments in Polarized CACO-2 Epithelial Cells

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1999 Aug 12
PMID 10444072
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

We have previously shown that a thin ( approximately 1 microm) layer of intermediate filaments located beneath the apical membrane of a variety of simple epithelial cells participates in the organization of apical microfilaments and microtubules. Here, I confirmed the apical distribution of gamma-tubulin-containing structures (potential microtubule-organizing centers) in CACO-2 cells and demonstrated perfect colocalization of centrosomes and nearly 50% of noncentrosomal gamma-tubulin with apical intermediate filaments, but not with apical F-actin. Furthermore, the antisense-oligonucleotide-mediated downregulation of cytokeratin 19, using two different antisense sequences, was more efficient than anticytoskeletal agents to delocalize centrosomes. Electron microscopy colocalization suggests that binding occurs at the outer boundary of the pericentriolar material. Type I cytokeratins 18 and 19 present in these cells specifically coimmunoprecipitated in multi-protein fragments of the cytoskeleton with gamma-tubulin. The size and shape of the fragments, visualized at the EM level, indicate that physical trapping is an unlikely explanation for this result. Drastic changes in the extraction protocol did not affect coimmunoprecipitation. These results from three independent techniques, indicate that insoluble gamma-tubulin-containing structures are attached to apical intermediate filaments.

Citing Articles

MCC is a centrosomal protein that relocalizes to non-centrosomal apical sites during intestinal cell differentiation.

Tomaz L, Liu B, Meroshini M , Ong S, Tan E, Tolwinski N J Cell Sci. 2022; 135(21).

PMID: 36217793 PMC: 10658790. DOI: 10.1242/jcs.259272.


AMPK-dependent phosphorylation of cingulin reversibly regulates its binding to actin filaments and microtubules.

Yano T, Torisawa T, Oiwa K, Tsukita S Sci Rep. 2018; 8(1):15550.

PMID: 30341325 PMC: 6195624. DOI: 10.1038/s41598-018-33418-7.


Genetically induced microtubule disruption in the mouse intestine impairs intracellular organization and transport.

Muroyama A, Terwilliger M, Dong B, Suh H, Lechler T Mol Biol Cell. 2018; 29(13):1533-1541.

PMID: 29742015 PMC: 6080650. DOI: 10.1091/mbc.E18-01-0057.


Microtubule organization, dynamics and functions in differentiated cells.

Muroyama A, Lechler T Development. 2017; 144(17):3012-3021.

PMID: 28851722 PMC: 5611961. DOI: 10.1242/dev.153171.


Intermediate Filaments and Polarization in the Intestinal Epithelium.

Coch R, Leube R Cells. 2016; 5(3).

PMID: 27429003 PMC: 5040974. DOI: 10.3390/cells5030032.


References
1.
Zheng Y, Wong M, Alberts B, Mitchison T . Nucleation of microtubule assembly by a gamma-tubulin-containing ring complex. Nature. 1995; 378(6557):578-83. DOI: 10.1038/378578a0. View

2.
Salas P, Rodriguez-Boulan E . Modulation of the expression of an apical plasma membrane protein of Madin-Darby canine kidney epithelial cells: cell-cell interactions control the appearance of a novel intracellular storage compartment. J Cell Biol. 1987; 104(5):1249-59. PMC: 2114464. DOI: 10.1083/jcb.104.5.1249. View

3.
Salas P, Rodriguez M, Viciana A, Hauri H . The apical submembrane cytoskeleton participates in the organization of the apical pole in epithelial cells. J Cell Biol. 1997; 137(2):359-75. PMC: 2139782. DOI: 10.1083/jcb.137.2.359. View

4.
Grindstaff K, Bacallao R, Nelson W . Apiconuclear organization of microtubules does not specify protein delivery from the trans-Golgi network to different membrane domains in polarized epithelial cells. Mol Biol Cell. 1998; 9(3):685-99. PMC: 25297. DOI: 10.1091/mbc.9.3.685. View

5.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View