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  1. In Vitro Cellular & Developmental Biology - Animal
  2. In Vitro Cellular & Developmental Biology - Animal : Volume 37
  3. In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 4, April 2001
  4. Cryopreservation of heart cells from the eastern oyster
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In Vitro Cellular & Developmental Biology - Animal : Volume 53
In Vitro Cellular & Developmental Biology - Animal : Volume 52
In Vitro Cellular & Developmental Biology - Animal : Volume 51
In Vitro Cellular & Developmental Biology - Animal : Volume 50
In Vitro Cellular & Developmental Biology - Animal : Volume 49
In Vitro Cellular & Developmental Biology - Animal : Volume 48
In Vitro Cellular & Developmental Biology - Animal : Volume 47
In Vitro Cellular & Developmental Biology - Animal : Volume 46
In Vitro Cellular & Developmental Biology - Animal : Volume 45
In Vitro Cellular & Developmental Biology - Animal : Volume 44
In Vitro Cellular & Developmental Biology - Animal : Volume 43
In Vitro Cellular & Developmental Biology - Animal : Volume 42
In Vitro Cellular & Developmental Biology - Animal : Volume 41
In Vitro Cellular & Developmental Biology - Animal : Volume 40
In Vitro Cellular & Developmental Biology - Animal : Volume 39
In Vitro Cellular & Developmental Biology - Animal : Volume 38
In Vitro Cellular & Developmental Biology - Animal : Volume 37
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 10, November 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 9, October 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 8, September 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 7, July 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 6, June 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 5, May 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 4, April 2001
Impairment of antigen-specific cellular immune responses under simulated microgravity conditions
Simulated microgravity impairs respiratory burst activity in human promyelocytic cells
Characteristics of human dendritic cells generated in a microgravity analog culture system
Epstein-barr virus latently infected cells are selectively deleted in simulated-microgravity cultures
Normal human liver organ culture
Human keratinocytes express functional α-MSH (MC1-R) receptors
Cryopreservation of heart cells from the eastern oyster
Transforming growth factor beta may act as an autocrine-survival-promoting factor for transformed trophoblasts
Renal cell cultures for the study of growth factor interactions underlying kidney organogenesis
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 3, March 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 2, February 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 37, Issue 1, January 2001
In Vitro Cellular & Developmental Biology - Animal : Volume 36
In Vitro Cellular & Developmental Biology - Animal : Volume 35
In Vitro Cellular & Developmental Biology - Animal : Volume 34
In Vitro Cellular & Developmental Biology - Animal : Volume 33

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Cryopreservation of heart cells from the eastern oyster

Content Provider Springer Nature Link
Author Cheng, Ta Chih Peyre, Jerome F. Buchanan, John T. Tiersch, Terrence R. Cooper, Richard K.
Copyright Year 2001
Abstract Conditions were developed to cryopreserve cells from pronase-dissociated atria and ventricles of eastern oysters (Crassostrea virginica). The effect of three concentrations (5, 10, 15%) of the cryoprotectants (dimethyl sulfoxide, glycerol, and propylene glycol), three thawing temperatures (25, 45, 75°C), and three cooling rates (slow, medium, fast) were compared. Cells were frozen at −80°C and plunged in liquid nitrogen. Thawed cells were seeded in 96-well plates and primary cultures were evaluated after 3 d by measuring the metabolic activity using a tetrazolium compound, 3-(4,5-dimethylthiazol-2-yl)-5-( 3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, and by comparing the relative spreading of cells between treatments. The best conditions for freezing and thawing of cells for each cryoprotectant were selected and a final study was performed to compare cryoprotectants. For this final study, we measured the number of cells and their viability 3 d after thawing, in addition to determining cell metabolic activity and cell spreading. Primary cultures of cells frozen without cryoprotectant and of nonfrozen cells were used as controls in all studies. Atrial cells were best cryopreserved with glycerol at a concentration of 10%, a medium cooling rate, and thawing at 45°C. After thawing, atrial cells showed 53±5% of the metabolic activity, 84±5% of the number, and 92±2% of the viability of nonfrozen cells. For ventricular cells, 10% glycerol, a medium cooling rate, and thawing at 25°C yielded the best results. The thawed ventricular cells showed 83±5% of the metabolic activity, 91±5% of the number, and 96±2% of the viability of nonfrozen cells.
Starting Page 237
Ending Page 243
Page Count 7
File Format PDF
ISSN 10712690
Journal In Vitro Cellular & Developmental Biology - Animal
Volume Number 37
Issue Number 4
e-ISSN 1543706X
Language English
Publisher Springer-Verlag
Publisher Date 2001-01-01
Publisher Place Berlin, Heidelberg
Access Restriction One Nation One Subscription (ONOS)
Subject Keyword Crassostrea virginica bivalve mollusc somatic cells cultures Cell Biology Developmental Biology Animal Genetics and Genomics Animal Biochemistry Animal Physiology
Content Type Text
Resource Type Article
Subject Cell Biology Developmental Biology Medicine
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