Literature DB >> 15766744

Developmental biology meets materials science: Morphogenesis of biomineralized structures.

Fred H Wilt1.   

Abstract

Biomineralization is the process by which metazoa form hard minerals for support, defense, and feeding. The minerals so formed, e.g., teeth, bones, shells, carapaces, and spicules, are of considerable interest to chemists and materials scientists. The cell biology underlying biomineralization is not well understood. The study of the formation of mineralized structures in developing organisms offers opportunities for understanding some intriguing aspects of cell and developmental biology. Five examples of biomineralization are presented: (1) the formation of siliceous spicules and frustules in sponges and diatoms, respectively; (2) the structure of skeletal spicules composed of amorphous calcium carbonate in some tunicates; (3) the secretion of the prism and nacre of some molluscan shells; (4) the development of skeletal spicules of sea urchin embryos; and (5) the formation of enamel of vertebrate teeth. Some speculations on the cellular and molecular mechanisms that support biomineralization, and their evolutionary origins, are discussed.

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Year:  2005        PMID: 15766744     DOI: 10.1016/j.ydbio.2005.01.019

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  37 in total

1.  Mechanistic basis of otolith formation during teleost inner ear development.

Authors:  David Wu; Jonathan B Freund; Scott E Fraser; Julien Vermot
Journal:  Dev Cell       Date:  2011-02-15       Impact factor: 12.270

Review 2.  Culture of and experiments with sea urchin embryo primary mesenchyme cells.

Authors:  Bradley Moreno; Allessandra DiCorato; Alexander Park; Kellen Mobilia; Regina Knapp; Reiner Bleher; Charlene Wilke; Keith Alvares; Derk Joester
Journal:  Methods Cell Biol       Date:  2019-02-11       Impact factor: 1.441

3.  Integrating morphology and in vivo skeletal mobility with digital models to infer function in brittle star arms.

Authors:  Elizabeth G Clark; John R Hutchinson; Simon A F Darroch; Nicolás Mongiardino Koch; Travis R Brady; Sloane A Smith; Derek E G Briggs
Journal:  J Anat       Date:  2018-10-23       Impact factor: 2.610

4.  The small GTPase Arf6 regulates sea urchin morphogenesis.

Authors:  Nadezda A Stepicheva; Megan Dumas; Priscilla Kobi; Julie G Donaldson; Jia L Song
Journal:  Differentiation       Date:  2017-02-02       Impact factor: 3.880

5.  A dynamic history of gene duplications and losses characterizes the evolution of the SPARC family in eumetazoans.

Authors:  Stephanie Bertrand; Jaime Fuentealba; Antoine Aze; Clare Hudson; Hitoyoshi Yasuo; Marcela Torrejon; Hector Escriva; Sylvain Marcellini
Journal:  Proc Biol Sci       Date:  2013-02-27       Impact factor: 5.349

Review 6.  Morphogenesis in sea urchin embryos: linking cellular events to gene regulatory network states.

Authors:  Deirdre C Lyons; Stacy L Kaltenbach; David R McClay
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2011-12-27       Impact factor: 5.814

7.  Transcellular calcium transport in mammary epithelial cells.

Authors:  Joshua N VanHouten; John J Wysolmerski
Journal:  J Mammary Gland Biol Neoplasia       Date:  2007-11-13       Impact factor: 2.673

8.  A GATA2/3 gene potentially involved in larval shell formation of the Pacific oyster Crassostrea gigas.

Authors:  Gang Liu; Pin Huan; Baozhong Liu
Journal:  Dev Genes Evol       Date:  2015-07-11       Impact factor: 0.900

9.  Characterization of an endoplasmic reticulum-associated silaffin kinase from the diatom Thalassiosira pseudonana.

Authors:  Vonda Sheppard; Nicole Poulsen; Nils Kröger
Journal:  J Biol Chem       Date:  2009-11-04       Impact factor: 5.157

Review 10.  Branching out: origins of the sea urchin larval skeleton in development and evolution.

Authors:  Daniel C McIntyre; Deirdre C Lyons; Megan Martik; David R McClay
Journal:  Genesis       Date:  2014-03-05       Impact factor: 2.487

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