Literature DB >> 16095930

Fibrin clots keep non-adhering living cells in place on glass for perfusion or fixation.

Arthur Forer1, Jeremy Pickett-Heaps.   

Abstract

We describe a method to hold living cells in place that ordinarily do not adhere to glass coverslips. The method, developed for insect spermatocytes but with application to other cell types, consists of embedding cells in a fibrin clot that forms after the enzyme thrombin cleaves the blood protein fibrinogen. The method permits continuous observation of living cells as they are treated with and recover from drug or other treatments: when held in the clot the living cells remain in place and keep their shapes when perfused with drugs that ordinarily cause drastic shape changes, and they remain in place and keep their shapes through lysis/fixation procedures. We describe how to place live cells in a fibrin clot and how subsequently to perfuse them.

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Year:  2005        PMID: 16095930     DOI: 10.1016/j.cellbi.2005.04.010

Source DB:  PubMed          Journal:  Cell Biol Int        ISSN: 1065-6995            Impact factor:   3.612


  14 in total

1.  Meiosis-I in Mesostoma ehrenbergii spermatocytes includes distance segregation and inter-polar movements of univalents, and vigorous oscillations of bivalents.

Authors:  Jessica Ferraro-Gideon; Carina Hoang; Arthur Forer
Journal:  Protoplasma       Date:  2013-08-07       Impact factor: 3.356

2.  Distance segregation of sex chromosomes in crane-fly spermatocytes studied using laser microbeam irradiations.

Authors:  Arthur Forer; Jessica Ferraro-Gideon; Michael Berns
Journal:  Protoplasma       Date:  2013-01-13       Impact factor: 3.356

3.  Single-cell Resolution Fluorescence Live Imaging of Drosophila Circadian Clocks in Larval Brain Culture.

Authors:  Virginie Sabado; Emi Nagoshi
Journal:  J Vis Exp       Date:  2018-01-19       Impact factor: 1.355

4.  Chromosomes selectively detach at one pole and quickly move towards the opposite pole when kinetochore microtubules are depolymerized in Mesostoma ehrenbergii spermatocytes.

Authors:  Eleni Fegaras; Arthur Forer
Journal:  Protoplasma       Date:  2018-02-21       Impact factor: 3.356

5.  Precocious cleavage furrows simultaneously move and ingress when kinetochore microtubules are depolymerized in Mesostoma ehrenbergii spermatocytes.

Authors:  Eleni Fegaras; Arthur Forer
Journal:  Protoplasma       Date:  2018-03-21       Impact factor: 3.356

6.  Possible roles of actin and myosin during anaphase chromosome movements in locust spermatocytes.

Authors:  Lacramioara Fabian; Arthur Forer
Journal:  Protoplasma       Date:  2007-10-10       Impact factor: 3.356

7.  Actin and myosin inhibitors block elongation of kinetochore fibre stubs in metaphase crane-fly spermatocytes.

Authors:  A Forer; T Spurck; J D Pickett-Heaps
Journal:  Protoplasma       Date:  2007-12-19       Impact factor: 3.356

8.  Calyculin A, an enhancer of myosin, speeds up anaphase chromosome movement.

Authors:  Lacramioara Fabian; Joanna Troscianczuk; Arthur Forer
Journal:  Cell Chromosome       Date:  2007-03-24

9.  Measurements of forces produced by the mitotic spindle using optical tweezers.

Authors:  Jessica Ferraro-Gideon; Rozhan Sheykhani; Qingyuan Zhu; Michelle L Duquette; Michael W Berns; Arthur Forer
Journal:  Mol Biol Cell       Date:  2013-03-13       Impact factor: 4.138

10.  Phospholipase C and myosin light chain kinase inhibition define a common step in actin regulation during cytokinesis.

Authors:  Raymond Wong; Lacramioara Fabian; Arthur Forer; Julie A Brill
Journal:  BMC Cell Biol       Date:  2007-05-17       Impact factor: 4.241

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