Literature DB >> 28305654

Fluorescent latex microparticles: A non-invasive short-term cell lineage marker suitable for use in the mouse early embryo.

Tom P Fleming1, Martin A George1.   

Abstract

We have examined the potential of fluorescent latex microparticles for use as a short term cell lineage marker in the mouse preimplantation embryo. Isolated blastomeres and intact embryos rapidly adsorb and subsequently endocytose the particles (0.2 μm diameter) from a monodisperse suspension in normal medium, so that cytoplasmic endocytic organelles, but not the cytosol itself, becomes labelled. Latex fluorescence, either within intact embryos, disaggregated cells or thick resin sections, is stable during UV irradiation. The development of labelled embryos, both in terms of sequential morphological changes and their time of expression, was comparable to controls and resulted in blastocysts with normal cell numbers and capacity for tissue differentiation. Latex fluorescence is preserved within all the progeny of labelled blastomeres over several cell cycles (e.g. from 8-cell stage to 64-cell stage) and is not transmitted to unlabelled cells either by exocytosis or via midbodies. The particles are particularly suitable for labelling exclusively the entire population of outside cells in the intact embryo from the 16-cell stage onwards.

Entities:  

Keywords:  Cell lineage; Fluorescent latex microparticles; Mouse embryos

Year:  1987        PMID: 28305654     DOI: 10.1007/BF00376016

Source DB:  PubMed          Journal:  Rouxs Arch Dev Biol        ISSN: 0930-035X


  40 in total

1.  Investigations into the degree of cell mixing that occurs between the 8-cell stage and the blastocyst stage of mouse development.

Authors:  S J Kelly
Journal:  J Exp Zool       Date:  1979-01

2.  Preimplantation differentiation in the mouse egg as revealed by microinjection of vital markers.

Authors:  I B Wilson; E Bolton; R H Cuttler
Journal:  J Embryol Exp Morphol       Date:  1972-04

3.  Cell division and cell allocation in early mouse development.

Authors:  S J Kelly; J G Mulnard; C F Graham
Journal:  J Embryol Exp Morphol       Date:  1978-12

4.  The roles of phenotype and position in guiding the fate of 16-cell mouse blastomeres.

Authors:  C A Ziomek; M H Johnson
Journal:  Dev Biol       Date:  1982-06       Impact factor: 3.582

5.  Changes in the distribution of membranous organelles during mouse early development.

Authors:  B Maro; M H Johnson; S J Pickering; D Louvard
Journal:  J Embryol Exp Morphol       Date:  1985-12

6.  Allocation of cells to inner cell mass and trophectoderm lineages in preimplantation mouse embryos.

Authors:  H Bałakier; R A Pedersen
Journal:  Dev Biol       Date:  1982-04       Impact factor: 3.582

7.  The use of fluorescein isothiocyanate (FITC) as a short-term cell lineage marker in the peri-implantation mouse embryo.

Authors:  Carol Ann Ziomek
Journal:  Wilehm Roux Arch Dev Biol       Date:  1982-01

8.  Molecular differentiation of inside cells and inner cell masses isolated from the preimplantation mouse embryo.

Authors:  M H Johnson
Journal:  J Embryol Exp Morphol       Date:  1979-10

9.  Temporal and spatial patterns of the synthesis of tissue-specific polypeptides in the preimplantation mouse embryo.

Authors:  A H Handyside; M H Johnson
Journal:  J Embryol Exp Morphol       Date:  1978-04

10.  A quantitative analysis of cell allocation to trophectoderm and inner cell mass in the mouse blastocyst.

Authors:  T P Fleming
Journal:  Dev Biol       Date:  1987-02       Impact factor: 3.582

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  3 in total

1.  Organisation and assembly of the surface membrane during early cleavage of the mouse embryo.

Authors:  Hester P M Pratt; Martin A George
Journal:  Rouxs Arch Dev Biol       Date:  1989-10

Review 2.  Developmental control of human preimplantation embryos: a comparative approach.

Authors:  J Tesarík
Journal:  J In Vitro Fert Embryo Transf       Date:  1988-12

3.  Plasticity of the inner cell mass in mouse blastocyst is restricted by the activity of FGF/MAPK pathway.

Authors:  M Wigger; K Kisielewska; K Filimonow; B Plusa; M Maleszewski; A Suwińska
Journal:  Sci Rep       Date:  2017-11-09       Impact factor: 4.379

  3 in total

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