2 edition of cell surface: its molecular role in morphogenesis found in the catalog.
cell surface: its molecular role in morphogenesis
A. S. G. Curtis
Bibliography: p. 349-398.
|Statement||[by] A. S. G. Curtis.|
|LC Classifications||QH601 .C86|
|The Physical Object|
|Pagination||x, 405 p.|
|Number of Pages||405|
|LC Control Number||67021470|
SUMMARY A living cell is not an aggregate of molecules but an organized pattern, structured in space and in time. This article addresses some conceptual issues in the genesis of spatial architecture, including how molecules find their proper location in cell space, the origins of supramolecular order, the role of the genes, cell morphology, the continuity of cells, and the Cited by: Multicellular organisms contain a large number of formins; however, their physiological roles in plants remain poorly understood. Here, we reveal that formin homology 5 (FH5), a type II formin mutated in rice morphology determinant (rmd), plays a crucial role in determining rice (Oryza sativa) morphology. FH5/RMD encodes a formin-like protein consisting of an N-terminal phosphatase tensin Cited by:
Contractile force generation: from molecules to tissues. While D'Arcy Thompson dismissed ʻthe many theories and speculations which would connect the phenomena of surface-tension with contractility [and] muscular movement' (p. , Thompson, ), we now understand that this connection is r, the tension at cell surfaces is not driven by surface tension, as Cited by: The female reproductive organ of angiosperms, the gynoecium, often consists of the fusion of multiple ovule-bearing carpels. It serves the important function of producing and protecting ovules as well as mediating pollination. The gynoecium has likely contributed to the tremendous success of angiosperms over their million year history. In addition, being a highly complex plant organ, the Cited by:
and why such changes occur, obviating the possibility of scientiﬁcally testing its hypothesized role in evolution. Since the late s, the determination of growth and differentiation by soluble growth factor-mediated cell-cell signaling has been acknowledged to be the mechanism of by: Hippo signaling is a critical pathway that integrates extrinsic and intrinsic mechanical cues to regulate organ size. Despite its essential role in organogenesis, little is known about its role in cell fate specification and differentiation. Here, we unravel a novel and unexpected role of the Hippo pathway effector Taz (wwtr1) in controlling the size, shape and fate of a unique cell in the Cited by: 6.
Escrow Principles and Practices
The European Social Model
Edwin D. Wescott.
Clinical Electrophysiology of the Heart (Current Topics in Cardiovascular Medicine, Vol 1)
A call to conscience
Spalding and the enlightenment
Compensation/human resource committees of boards of directors
continuity of the Church of England
Get this from a library. The cell surface: its molecular role in morphogenesis. [A S G Curtis]. Cell surface: its molecular role in morphogenesis.
London, Logos Press; New York, Academic Press [ (OCoLC) Online version: Curtis, A.S.G. Cell surface: its molecular role in morphogenesis. London, Logos Press; New York, Academic Press [ (OCoLC) Document Type: Book: All Authors / Contributors: A S G Curtis.
Cell–cell contacts change the shape of cells such that they are no longer spherical. Single cells, such as mouse embryonic cells at the two-cell stage with a b-catenin mutation that disrupts E Cited by: Morphogenesis (from the Greek morphê shape and genesis creation, literally, "beginning of the shape") is the biological process that causes an organism to develop its shape.
It is one of three fundamental aspects of developmental biology along with the control of cell growth and cellular differentiation, unified in evolutionary developmental biology (evo-devo). Sagner, in Methods in Cell Biology, Abstract.
Morphogenesis of an epithelial tissue emerges from the behavior of its constituent cells, including changes in shape, rearrangements, and divisions. In many instances the directionality of these cellular events is controlled by the polarized distribution of specific molecular components.
The cell surface looks pretty much the same in all cell types, and many early investigators thought that the cell surface was not even a living part of the cell. We now know that each type of cell has a different set of proteins in its surfaces, and that some of these differences are responsible for forming the structure of the tissues and Cited by: 2.
Paul W. Finch, Jeffrey S. Rubin, in Advances in Cancer Research, D Branching Morphogenesis. Epithelial branching morphogenesis is a highly coordinated process involving cell proliferation, cell–cell and cell–matrix interactions, and remodeling of the basement membrane.
A number of studies have demonstrated that KGF can stimulate growth and branching morphogenesis in various fetal. The book starts with a discussion of molecular self-assembly and its limitations before moving on to the cytoskeleton in all its richness.
There are then chapters on the shapes of cells and plant morphogenesis (a novel area for me) before the book really gets into its stride with a long section on cell migration, which covers the intracellular Author: Jonathan Bard.
This book provides an overview of critical components of cell signaling machinery and its role in epithelial morphogenesis, proliferation, invasions and angiogenesis in human cancer and discusses.
Heavily sialylated adhesion molecules found on leukocytes and cells in the nervous system. These molecules are usually large and strongly negatively charged, so they tend to prevent other cells from approaching and interacting, unless the other cell has specific receptors for the sialoadhesin, or, alternatively, other pairs of adhesion molecules that mediate cell-cell interactions are present.
Little is known about endocardial chamber morphogenesis. Dietrich et al. show that the endocardium is flow sensitive and has a role in adapting heart chamber growth in response to the mechanical stimulus of blood flow.
Endocardial growth also requires Bmp signaling in a Cited by: The activation process for the epidermal growth factor receptor (EGFR) involves formation of an asymmetric dimer of the tyrosine kinase domains.
Jura et al. () in this issue and Brewer et al. () in Molecular Cell now demonstrate that the juxtamembrane region of EGFR plays a crucial role in stabilizing this dimer. The Role of the Primary Cell Wall in Plant Morphogenesis. June for future studies of this model organism in cell and molecular biology.
predominantly at the lateral cell surface. PIN3. in the developing embryo. The matrix on a cell surface will be changed after each cell event according to the rule(s) dictated by the morphogenetic field of an organism. Finally, we provide some ideas about the connection between the morphogenetic code on the cell surface, cell motion law(s), and the geometry of.
Bacterial Cell-to-Cell Communication Role in Virulence and Pathogenesis. Chapter. 11 - Signaling by a cell-surface-associated signal during fruiting-body morphogenesis in Myxococcus xanthus.
By Lotte Søgaard-Andersen, Max Planck Institute for Terrestrial The C-signal is a 17 kDa cell-surface-associated protein and is thus Author: Lotte Søgaard-Andersen. Al Jumaa MA, Dewitt S, Hallett MB () Topographical interrogation of the living cell surface reveals its role in rapid cell shape changes during phagocytosis and spreading.
Sci Rep PubMed PubMedCentral CrossRef Google Scholar. The Polycystins in Cell Migration, Polarity, and Tissue Morphogenesis The involvement of PC-1 in regulating cell migration and cellular morphogenesis has been demonstrated by different groups.
The over-expression of the PKD1 cDNA in Madin Darby canine kidney (MDCKtypeII) cells was reported to induce spontaneous tubulogenesis when cells are Cited by: Proper fusion involves cell rearrangements and cell convergence movements (Kim et al., ), similar to convergence and extension morphogenesis in gastrulating embryos (Keller, ), which we previously showed to depend on cell surface cadherin regulation (Brieher and Gumbiner, ; Zhong et al., ).
Thus, whereas basal adhesive activity. Lobes Can Be Initiated at a Substantially Reduced Degree of Cellulose Crystallinity. To understand the role of crystalline cellulose during lobe development, we investigated pavement cell shape in cotyledons of wild-type Arabidopsis and of the any1 mutant (Fig.
1A; Supplemental Fig. S1).The total content of cellulose in the cell wall of this mutant was reported to be unaltered, while the Cited by: 8.
Molecular Biology of the Cell Vol. 17, No. 1 Articles Free Access From Function to Shape: A Novel Role of a Formin in Morphogenesis of the Fungus Ashbya gossypii This is the final version -. The role of RG-I in the mechanical properties of the plant cell wall is only poorly understood even if it has been implicated in cell wall extensibility and firmness.
Using RG-I-specific antibodies, McCartney et al. () observed that in pea cotyledons galactan-rich RG-I appears in the inner face of the cell wall at later stages of Cited by: The assembly of these multicellular structures during embryo development involves highly dynamic changes in cell-cell adhesion and cell migration that appear to rely on remodelling of the actin cytoskeleton and of its links with adhesion molecules.
Our goal is to understand the cellular and molecular mechanisms underlying such remodelling events. Actin microfilaments form a three-dimensional cytoskeletal network throughout the cell and constitute an essential throughway for organelle and vesicle transport.
Development of Arabidopsis trichomes, unicellular structures derived from the epidermis, is being used as a genetic system in which to study actin-dependent growth in plant cells. The present study indicates that filamentous actin (F Cited by: