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1.
Development ; 146(2)2019 01 23.
Artigo em Inglês | MEDLINE | ID: mdl-30630824

RESUMO

The enrichment of intermediate filaments in the apical cytoplasm of intestinal cells is evolutionarily conserved, forming a sheath that is anchored to apical junctions and positioned below the microvillar brush border, which suggests a protective intracellular barrier function. To test this, we used Caenorhabditiselegans, the intestinal cells of which are endowed with a particularly dense intermediate filament-rich layer that is referred to as the endotube. We found alterations in endotube structure and intermediate filament expression upon infection with nematicidal B.thuringiensis or treatment with its major pore-forming toxin crystal protein Cry5B. Endotube impairment due to defined genetic mutations of intermediate filaments and their regulators results in increased Cry5B sensitivity as evidenced by elevated larval arrest, prolonged time of larval development and reduced survival. Phenotype severity reflects the extent of endotube alterations and correlates with reduced rescue upon toxin removal. The results provide in vivo evidence for a major protective role of a properly configured intermediate filament network as an intracellular barrier in intestinal cells. This notion is further supported by increased sensitivity of endotube mutants to oxidative and osmotic stress.


Assuntos
Bacillus thuringiensis/fisiologia , Proteínas de Bactérias/toxicidade , Caenorhabditis elegans/microbiologia , Endotoxinas/toxicidade , Proteínas Hemolisinas/toxicidade , Filamentos Intermediários/metabolismo , Intestinos/microbiologia , Intestinos/patologia , Animais , Toxinas de Bacillus thuringiensis , Caenorhabditis elegans/genética , Caenorhabditis elegans/crescimento & desenvolvimento , Caenorhabditis elegans/ultraestrutura , Proteínas de Caenorhabditis elegans/metabolismo , Imunidade Inata/efeitos dos fármacos , Imunidade Inata/genética , Filamentos Intermediários/efeitos dos fármacos , Intestinos/efeitos dos fármacos , Larva/efeitos dos fármacos , Larva/ultraestrutura , Mutação/genética , Pressão Osmótica/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Isoformas de Proteínas/metabolismo , Transcrição Gênica/efeitos dos fármacos
2.
Int J Mol Sci ; 21(21)2020 11 03.
Artigo em Inglês | MEDLINE | ID: mdl-33153048

RESUMO

The intestine is an organ essential to organismal nutrient absorption, metabolic control, barrier function and immunoprotection. The Caenorhabditis elegans intestine consists of 20 cells harboring a dense intermediate filament network positioned below the apical plasma membrane that forms a junction-anchored sheath around the intestinal lumen. This evolutionarily conserved arrangement provides mechanical and overall stress-protection, and it serves as an important model for deciphering the role of intestinal architecture in metazoan biology. We recently reported that the loss-of-function mutation of the intestinal intermediate filament organizer IFO-1 perturbs this architecture, leading to reduced body size and reproduction. Here, we demonstrate that the IFO-1 mutation dramatically affects cholesterol metabolism. Mutants showed an increased sensitivity to cholesterol depletion, reduced cholesterol uptake, and cholesterol transfer to the gonads, which is also observed in worms completely lacking an intermediate filament network. Accordingly, we found striking similarities to transcriptome and lipidome profiles of a nuclear hormone receptor (NHR)-8 mutant. NHR-8 is homologous to mammalian LXR (liver X receptor) that serves as a sterol sensor and transcriptional regulator of lipid metabolism. Remarkably, increasing exogenous cholesterol partially rescues the developmental retardation in IFO-1 mutants. Our results uncover a novel link of the intestinal intermediate filament cytoskeleton to cholesterol metabolism that contributes to compromised growth and reproduction.


Assuntos
Proteínas de Caenorhabditis elegans/metabolismo , Caenorhabditis elegans , Colesterol/metabolismo , Proteínas de Filamentos Intermediários/genética , Metabolismo dos Lipídeos/genética , Animais , Animais Geneticamente Modificados , Caenorhabditis elegans/efeitos dos fármacos , Caenorhabditis elegans/embriologia , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , Proteínas de Caenorhabditis elegans/genética , Colesterol/farmacologia , Embrião não Mamífero , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Proteínas de Filamentos Intermediários/metabolismo , Filamentos Intermediários/metabolismo , Mucosa Intestinal/embriologia , Mucosa Intestinal/metabolismo , Mucosa Intestinal/ultraestrutura , Intestinos/embriologia , Intestinos/fisiologia , Intestinos/ultraestrutura , Metabolismo dos Lipídeos/efeitos dos fármacos , Lipidômica , Receptores Citoplasmáticos e Nucleares/fisiologia , Transcriptoma/efeitos dos fármacos
3.
Elife ; 122023 06 07.
Artigo em Inglês | MEDLINE | ID: mdl-37283438

RESUMO

Intermediate filaments (IFs) are major components of the metazoan cytoskeleton. A long-standing debate concerns the question whether IF network organization only reflects or also determines cell and tissue function. Using Caenorhabditis elegans, we have recently described mutants of the mitogen-activated protein kinase (MAPK) SMA-5 which perturb the organization of the intestinal IF cytoskeleton resulting in luminal widening and cytoplasmic invaginations. Besides these structural phenotypes, systemic dysfunctions were also observed. We now identify the IF polypeptide IFB-2 as a highly efficient suppressor of both the structural and functional deficiencies of mutant sma-5 animals by removing the aberrant IF network. Mechanistically, perturbed IF network morphogenesis is linked to hyperphosphorylation of multiple sites throughout the entire IFB-2 molecule. The rescuing capability is IF isotype-specific and not restricted to sma-5 mutants but extends to mutants that disrupt the function of the cytoskeletal linker IFO-1 and the IF-associated protein BBLN-1. The findings provide strong evidence for adverse consequences of the deranged IF networks with implications for diseases that are characterized by altered IF network organization.


Assuntos
Proteínas de Caenorhabditis elegans , Filamentos Intermediários , Animais , Filamentos Intermediários/metabolismo , Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/metabolismo , Intestinos , Citoesqueleto/metabolismo
4.
Methods Enzymol ; 568: 681-706, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26795489

RESUMO

It is commonly accepted that intermediate filaments have an important mechanical function. This function relies not only on intrinsic material properties but is also determined by dynamic interactions with other cytoskeletal filament systems, distinct cell adhesion sites, and cellular organelles which are fine-tuned by multiple signaling pathways. While aspects of these properties and processes can be studied in vitro, their full complexity can only be understood in a viable tissue context. Yet, suitable and easily accessible model systems for monitoring tissue mechanics at high precision are rare. We show that the dissected intestine of the genetic model organism Caenorhabditis elegans fulfills this requirement. The 20 intestinal cells, which are arranged in an invariant fashion, are characterized by a dense subapical mesh of intermediate filaments that are attached to the C. elegans apical junction. We present procedures to visualize details of the characteristic intermediate filament-junctional complex arrangement in living animals. We then report on methods to prepare intestines with a fully intact intermediate filament cytoskeleton and detail procedures to assess their viability. A dual micropipette assay is described to measure mechanical properties of the dissected intestine while monitoring the spatial arrangement of the intermediate filament system. Advantages of this approach are (i) the high reproducibility of measurements because of the uniform architecture of the intestine and (ii) the high degree of accessibility allowing not only mechanical manipulation of an intact tissue but also control of culture medium composition and addition of drugs as well as visualization of cell structures. With this method, examination of worms carrying mutations in the intermediate filament system, its interacting partners and its regulators will become feasible.


Assuntos
Caenorhabditis elegans/metabolismo , Filamentos Intermediários/metabolismo , Mucosa Intestinal/metabolismo , Animais
5.
Cells ; 5(3)2016 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-27429003

RESUMO

The cytoplasmic intermediate filament cytoskeleton provides a tissue-specific three-dimensional scaffolding with unique context-dependent organizational features. This is particularly apparent in the intestinal epithelium, in which the intermediate filament network is localized below the apical terminal web region and is anchored to the apical junction complex. This arrangement is conserved from the nematode Caenorhabditis elegans to humans. The review summarizes compositional, morphological and functional features of the polarized intermediate filament cytoskeleton in intestinal cells of nematodes and mammals. We emphasize the cross talk of intermediate filaments with the actin- and tubulin-based cytoskeleton. Possible links of the intermediate filament system to the distribution of apical membrane proteins and the cell polarity complex are highlighted. Finally, we discuss how these properties relate to the establishment and maintenance of polarity in the intestine.

6.
Artigo em Coreano | WPRIM | ID: wpr-76138

RESUMO

Post-intubation croup and tidal volme leak during ventilator support may occur when unsuitable size of endotracheal tube is used. Malposition of endotracheal tubes(ETT) are particularly common in pediatric ICU patients, and may lead to serious complications such as inadvertent endobronchial intubation and accidental extubation. Due to the inaccuracy of physical examination for ETT placement and although there is additional time consumption and expense, the chest X-ray is still considered the gold standard for ETT position evaluation. We assessed the predetermined endotracheal tube size and the distance from the incisor to the carina according to the patient's age, weight and height. The chest X-ray was used for evaluation of these patients who were admitted to the intensive care unit of Severance Hospital Yonsei Medical Center from March to August, 1990. We divided the 430 intubated patients into two groups. Group 1 included 163 patents who were intubated by a endotracheal tube without a cuff. Group 2 included 237 patients who were intubated by a endotracheal tube with a cuff. The conclusion from our results were as follows: 1) The coefficient of determination of the endotracheal tube size, R(2), was highest according to weight, 0.40 and 0.50 in Group 1 and 2. The regression equation of endotracheal tube size using weight was Y=0.11X+3.42 and Y=0.04X+5.46 in Group 1 and Group 2. 2) The coefficient of determination of the distance from the incisor to the carina was highest according to weight 0.57 and 0.33 in Group I and 2. The regression equation of the distance from the incisor to the carina using weight was Y=0.47+10.74 and Y=0.11X+20.17.


Assuntos
Humanos , Crupe , Incisivo , Unidades de Terapia Intensiva , Intubação , Exame Físico , Tórax , Ventiladores Mecânicos
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