Literature DB >> 18623245

Death mechanisms of animal cells in conditions of intensive agitation.

M Al-Rubeai1, R P Singh, M H Goldman, A N Emery.   

Abstract

The question is addressed as to whether cells which are subject to high-energy dissipation rates in agitated bioreactors show an apoptotic response. Murine hybridoma cells in batch culture were agitated in bench-scale (1-L) bioreactors without gas sparging. At an energy dissipation rate of 1.5 W m(-3) there was no apparent damage. At 320 W m(-3) cell viability declined, and increasing proportions of the dead cells displayed the morphological features of apoptosis, but necrosis also remained as a significant mechanism of death. When cells were subjected to the intensive energy dissipation rate of 1870 W m(-3) in a bioreactor without gas headspace, the cell number dropped by 50% within 2 h and a subpopulation of smaller-sized cells emerged. This excluded trypan blue but showed some apoptotic characteristics such as reduced and condensed DNA content and low F-actin content. The incidence of apoptotic activity was further demonstrated by the appearance of numerous apoptotic bodies. Analysis of the cell cycles of both small and normal size populations indicated that greater proportions of S and G2 cells had become apoptotic and there was evidence of preferential survival of G1 cells. It is suggested that two mechanisms of cell death are apparent in hydrodynamically stressful situations, but their relative expression depends on the energy dissipation rate.

Entities:  

Year:  1995        PMID: 18623245     DOI: 10.1002/bit.260450602

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  17 in total

1.  Cell death in mammalian cell culture: molecular mechanisms and cell line engineering strategies.

Authors:  Britta Krampe; Mohamed Al-Rubeai
Journal:  Cytotechnology       Date:  2010-05-26       Impact factor: 2.058

Review 2.  Living with heterogeneities in bioreactors: understanding the effects of environmental gradients on cells.

Authors:  Alvaro R Lara; Enrique Galindo; Octavio T Ramírez; Laura A Palomares
Journal:  Mol Biotechnol       Date:  2006-11       Impact factor: 2.695

3.  Variable functions of bcl-2 in mediating bioreactor stress- induced apoptosis in hybridoma cells.

Authors:  A Perani; R P Singh; R Chauhan; M Al-Rubeai
Journal:  Cytotechnology       Date:  1998-11       Impact factor: 2.058

4.  Reactor design for large scale suspension animal cell culture.

Authors:  J Varley; J Birch
Journal:  Cytotechnology       Date:  1999-05       Impact factor: 2.058

5.  Albumin and mammalian cell culture: implications for biotechnology applications.

Authors:  Geoffrey L Francis
Journal:  Cytotechnology       Date:  2010-04-06       Impact factor: 2.058

6.  Cationic surface charge combined with either vitronectin or laminin dictates the evolution of human embryonic stem cells/microcarrier aggregates and cell growth in agitated cultures.

Authors:  Alan Tin-Lun Lam; Jian Li; Allen Kuan-Liang Chen; Shaul Reuveny; Steve Kah-Weng Oh; William R Birch
Journal:  Stem Cells Dev       Date:  2014-04-25       Impact factor: 3.272

7.  Separation of CHO cells using hydrocyclones.

Authors:  Rodrigo C V Pinto; Ricardo A Medronho; Leda R Castilho
Journal:  Cytotechnology       Date:  2007-11-14       Impact factor: 2.058

8.  Apoptosis and its suppression in hepatocytes culture.

Authors:  Nyaradzo T Mukwena; Mohamed Al-Rubeai
Journal:  Cytotechnology       Date:  2005-11-30       Impact factor: 2.058

9.  Regulated overexpression of the survival factor bcl-2 in CHO cells increases viable cell density in batch culture and decreases DNA release in extended fixed-bed cultivation.

Authors:  M Fussenegger; D Fassnacht; R Schwartz; J A Zanghi; M Graf; J E Bailey; R Pörtner
Journal:  Cytotechnology       Date:  2000-01       Impact factor: 2.058

10.  Stable transfection of CHO cells with the c-myc gene results in increased proliferation rates, reduces serum dependency, and induces anchorage independence.

Authors:  Vasiliki Ifandi; Mohamed Al-Rubeai
Journal:  Cytotechnology       Date:  2003-01       Impact factor: 2.058

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