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1.
J Cell Sci ; 136(5)2023 03 01.
Artículo en Inglés | MEDLINE | ID: mdl-36718636

RESUMEN

The regulation of mechanical tension exerted at cell junctions guides cell behavior during tissue formation and homeostasis. Cell junctions along compartment boundaries, which are lineage restrictions separating cells with different fates and functions within tissues, are characterized by increased mechanical tension compared to that of cell junctions in the bulk of the tissue. Mechanical tension depends on the actomyosin cytoskeleton; however, the mechanisms by which mechanical tension is locally increased at cell junctions along compartment boundaries remain elusive. Here, we show that non-muscle Myosin II and F-actin transiently accumulate and mechanical tension is increased at cell junctions along the forming anteroposterior compartment boundary in the Drosophila melanogaster pupal abdominal epidermis. Fluorescence recovery after photobleaching experiments showed that Myosin II accumulation correlated with its increased stabilization at these junctions. Moreover, photoconversion experiments indicated that Myosin II is preferentially recruited within cells to junctions along the compartment boundary. Our results indicate that the preferential recruitment and stabilization of Myosin II contribute to the initial build-up of mechanical tension at compartment boundaries.


Asunto(s)
Proteínas de Drosophila , Drosophila , Animales , Drosophila melanogaster , Estrés Mecánico , Miosina Tipo II , Actomiosina
2.
Development ; 147(5)2020 03 11.
Artículo en Inglés | MEDLINE | ID: mdl-32161061

RESUMEN

The replacement of cells is a common strategy during animal development. In the Drosophila pupal abdomen, larval epidermal cells (LECs) are replaced by adult progenitor cells (histoblasts). Previous work showed that interactions between histoblasts and LECs result in apoptotic extrusion of LECs during early pupal development. Extrusion of cells is closely preceded by caspase activation and is executed by contraction of a cortical actomyosin cable. Here, we identify a population of LECs that extrudes independently of the presence of histoblasts during late pupal development. Extrusion of these LECs is not closely preceded by caspase activation, involves a pulsatile medial actomyosin network, and correlates with a developmental time period when mechanical tension and E-cadherin turnover at adherens junctions is particularly high. Our work reveals a developmental switch in the cell extrusion mechanism that correlates with changes in tissue mechanical properties.


Asunto(s)
Abdomen/embriología , Drosophila melanogaster/citología , Drosophila melanogaster/crecimiento & desarrollo , Células Epidérmicas/citología , Epidermis/embriología , Uniones Adherentes/metabolismo , Animales , Animales Modificados Genéticamente , Cadherinas/metabolismo , Caspasas/metabolismo , Proliferación Celular , Larva/citología , Pupa/citología , Estrés Mecánico
3.
J Cell Sci ; 126(Pt 20): 4684-97, 2013 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-23943866

RESUMEN

The Hedgehog (Hh) signalling cascade is highly conserved and involved in development and disease throughout evolution. Nevertheless, in comparison with other pathways, our mechanistic understanding of Hh signal transduction is remarkably incomplete. In the absence of ligand, the Hh receptor Patched (Ptc) represses the key signal transducer Smoothened (Smo) through an unknown mechanism. Hh binding to Ptc alleviates this repression, causing Smo redistribution to the plasma membrane, phosphorylation and opening of the Smo cytoplasmic tail, and Smo oligomerisation. However, the order and interdependence of these events is as yet poorly understood. We have mathematically modelled and simulated Smo activation for two alternative modes of pathway activation, with Ptc primarily affecting either Smo localisation or phosphorylation. Visualising Smo activation through a novel, fluorescence-based reporter allowed us to test these competing models. Here, we show that Smo localisation to the plasma membrane is sufficient for phosphorylation of the cytoplasmic tail in the presence of Ptc. Using fluorescence cross-correlation spectroscopy (FCCS), we also demonstrate that inactivation of Ptc by Hh induces Smo clustering irrespective of Smo phosphorylation. Our observations therefore support a model of Hh signal transduction whereby Smo subcellular localisation and not phosphorylation is the primary target of Ptc function.


Asunto(s)
Proteínas de Drosophila/metabolismo , Proteínas Hedgehog/metabolismo , Receptores Acoplados a Proteínas G/metabolismo , Animales , Membrana Celular/metabolismo , Células Cultivadas , Análisis por Conglomerados , Drosophila , Endocitosis/fisiología , Modelos Biológicos , Fosforilación , Glándulas Salivales/metabolismo , Transducción de Señal , Receptor Smoothened , Espectrometría de Fluorescencia , Transfección
4.
Development ; 139(15): 2663-9, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22745310

RESUMEN

In the Drosophila testis, germline stem cells (GSCs) and somatic cyst stem cells (CySCs) are arranged around a group of postmitotic somatic cells, termed the hub, which produce a variety of growth factors contributing to the niche microenvironment that regulates both stem cell pools. Here we show that CySC but not GSC maintenance requires Hedgehog (Hh) signalling in addition to Jak/Stat pathway activation. CySC clones unable to transduce the Hh signal are lost by differentiation, whereas pathway overactivation leads to an increase in proliferation. However, unlike cells ectopically overexpressing Jak/Stat targets, the additional cells generated by excessive Hh signalling remain confined to the testis tip and retain the ability to differentiate. Interestingly, Hh signalling also controls somatic cell populations in the fly ovary and the mammalian testis. Our observations might therefore point towards a higher degree of organisational homology between the somatic components of gonads across the sexes and phyla than previously appreciated.


Asunto(s)
Proteínas Hedgehog/metabolismo , Células Madre/citología , Testículo/metabolismo , Animales , Diferenciación Celular , Proliferación Celular , Clonación Molecular , Cruzamientos Genéticos , Drosophila melanogaster , Femenino , Janus Quinasa 1/metabolismo , Masculino , Microscopía/métodos , Modelos Biológicos , Mutación , Factores de Transcripción STAT/metabolismo , Transducción de Señal
5.
Dev Cell ; 36(6): 589-90, 2016 Mar 21.
Artículo en Inglés | MEDLINE | ID: mdl-27003930

RESUMEN

A century ago, Oscar Hertwig discovered that cells orient their cleavage plane orthogonal to their long axis. Reporting recently in Nature, Bosveld et al. (2016) shed light on how, showing that NuMA/Mud localization at tricellular junctions provides mitotic cells with the memory of interphase shape used to orient cleavage plane.


Asunto(s)
Forma de la Célula , Drosophila melanogaster/citología , Células Epiteliales/citología , Uniones Intercelulares , Interfase , Mitosis , Animales , Femenino , Masculino
6.
Fly (Austin) ; 10(4): 204-9, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27362651

RESUMEN

During animal development, cells with similar function and fate often stay together and sort out from cells with different fates. In Drosophila wing imaginal discs, cells of anterior and posterior fates are separated by a straight compartment boundary. Separation of anterior and posterior cells requires the homeodomain-containing protein Engrailed, which is expressed in posterior cells. Engrailed induces the expression of the short-range signaling molecule Hedgehog in posterior cells and confines Hedgehog signal transduction to anterior cells. Transduction of the Hedgehog signal in anterior cells is required for the separation of anterior and posterior cells. Previous work showed that this separation of cells involves a local increase in mechanical tension at cell junctions along the compartment boundary. However, how mechanical tension was locally increased along the compartment boundary remained unknown. A recent paper now shows that the difference in Hedgehog signal transduction between anterior and posterior cells is necessary and sufficient to increase mechanical tension. The local increase in mechanical tension biases junctional rearrangements during cell intercalations to maintain the straight shape of the compartment boundary. These data highlight how developmental signals can generate patterns of mechanical tension important for tissue organization.


Asunto(s)
Drosophila/citología , Drosophila/crecimiento & desarrollo , Animales , Proteínas de Unión al ADN/metabolismo , Drosophila/metabolismo , Proteínas de Drosophila/metabolismo , Proteínas Hedgehog/metabolismo , Proteínas de Homeodominio , Discos Imaginales/metabolismo , Transducción de Señal , Factores de Transcripción/metabolismo , Alas de Animales/embriología , Alas de Animales/metabolismo
7.
PLoS One ; 11(8): e0161668, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27552097

RESUMEN

The separation of cells with distinct fates and functions is important for tissue and organ formation during animal development. Regions of different fates within tissues are often separated from another along straight boundaries. These compartment boundaries play a crucial role in tissue patterning and growth by stably positioning organizers. In Drosophila, the wing imaginal disc is subdivided into a dorsal and a ventral compartment. Cells of the dorsal, but not ventral, compartment express the selector gene apterous. Apterous expression sets in motion a gene regulatory cascade that leads to the activation of Notch signaling in a few cell rows on either side of the dorsoventral compartment boundary. Both Notch and apterous mutant clones disturb the separation of dorsal and ventral cells. Maintenance of the straight shape of the dorsoventral boundary involves a local increase in mechanical tension at cell bonds along the boundary. The mechanisms by which cell bond tension is locally increased however remain unknown. Here we use a combination of laser ablation of cell bonds, quantitative image analysis, and genetic mutants to show that Notch and Apterous are required to increase cell bond tension along the dorsoventral compartment boundary. Moreover, clonal expression of the Apterous target gene capricious results in cell separation and increased cell bond tension at the clone borders. Finally, using a vertex model to simulate tissue growth, we find that an increase in cell bond tension at the borders of cell clones, but not throughout the cell clone, can lead to cell separation. We conclude that Apterous and Notch maintain the characteristic straight shape of the dorsoventral compartment boundary by locally increasing cell bond tension.


Asunto(s)
Tipificación del Cuerpo/genética , Proteínas de Drosophila/genética , Drosophila/embriología , Drosophila/fisiología , Fenómenos Mecánicos , Receptores Notch/genética , Animales , Drosophila/anatomía & histología , Proteínas de Drosophila/metabolismo , Regulación del Desarrollo de la Expresión Génica , Modelos Teóricos , Receptores Notch/metabolismo , Selección Genética , Transducción de Señal , Estrés Mecánico
8.
Nat Commun ; 2: 415, 2011 Aug 02.
Artículo en Inglés | MEDLINE | ID: mdl-21811244

RESUMEN

According to the stem cell niche synapse hypothesis postulated for the mammalian haematopoietic system, spatial specificity of niche signals is maximized by subcellularly restricting signalling to cadherin-based adherens junctions between individual niche and stem cells. However, such a synapse has never been observed directly, in part, because tools to detect active growth factor receptors with subcellular resolution were not available. Here we describe a novel fluorescence-based reporter that directly visualizes bone morphogenetic protein (BMP) receptor activation and show that in the Drosophila testis a BMP niche signal is transmitted preferentially at adherens junctions between hub and germline stem cells, resembling the proposed synapse organization. Ligand secretion involves the exocyst complex and the Rap activator Gef26, both of which are also required for Cadherin trafficking towards adherens junctions. We, therefore, propose that local generation of the BMP signal is achieved through shared use of the Cadherin transport machinery.


Asunto(s)
Uniones Adherentes/metabolismo , Proteínas de Drosophila/metabolismo , Drosophila/metabolismo , Proteínas Serina-Treonina Quinasas/metabolismo , Receptores de Superficie Celular/metabolismo , Nicho de Células Madre , Testículo/citología , Uniones Adherentes/genética , Animales , Proteínas Morfogenéticas Óseas/metabolismo , Drosophila/genética , Proteínas de Drosophila/genética , Células Germinativas/citología , Células Germinativas/metabolismo , Masculino , Proteínas Serina-Treonina Quinasas/genética , Receptores de Superficie Celular/genética , Transducción de Señal , Células Madre/citología , Células Madre/metabolismo , Testículo/metabolismo
9.
Islets ; 1(3): 185-90, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-21099271

RESUMEN

Diabetes is a predominant metabolic disorder in the industrialized nations. Since pancreatic islets play a key role in type I and type II diabetes, the isolation of islets from pancreatic tissues represents an important step in diabetes research. However, to date, only a small fraction of all islets, resident within any given pancreas, are harvested by using currently available enzyme blends. This holds true for islet isolation from both the mouse and the human pancreas. In the present study, the newly developed Liberase TL Research Grade was compared to the widely used Liberase RI to investigate the effect of increased collagenase purity on islet yield. The study shows that reducing the degradation products of collagenases during Liberase production significantly increases the number of islets isolated from the mouse pancreas by 28%, and, therefore, is expected to lower the numbers of mice and resulting costs for diabetes research accordingly. Furthermore, this study also points to a possibility to increase the number and mass of islets isolated from human pancreases, for which only a limited donor pool exists.


Asunto(s)
Colagenasas/farmacología , Islotes Pancreáticos/citología , Islotes Pancreáticos/efectos de los fármacos , Páncreas/efectos de los fármacos , Animales , Recuento de Células , Separación Celular , Células Cultivadas , Cromatografía Líquida de Alta Presión , Colagenasas/química , Colagenasas/aislamiento & purificación , Combinación de Medicamentos , Humanos , Insulina/metabolismo , Islotes Pancreáticos/metabolismo , Masculino , Ratones , Páncreas/citología , Páncreas/metabolismo , Extractos de Tejidos/análisis , Extractos de Tejidos/farmacología , Regulación hacia Arriba/efectos de los fármacos
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