Effects of hypoxic culture conditions on umbilical cord-derived human mesenchymal stem cells


Autoria(s): Lavrentieva, Antonina; Majore, Ingrida; Kasper, Cornelia; Hass, Ralf
Data(s)

16/06/2010

Resumo

Following cultivation of distinct mesenchymal stem cell (MSC) populations derived from human umbilical cord under hypoxic conditions (between 1.5% to 5% oxygen (O-2)) revealed a 2- to 3-fold reduced oxygen consumption rate as compared to the same cultures at normoxic oxygen levels (21% O-2). A simultaneous measurement of dissolved oxygen within the culture media from 4 different MSC donors ranged from 15 mu mol/L at 1.5% O-2 to 196 mu mol/L at normoxic 21% O-2. The proliferative capacity of the different hypoxic MSC populations was elevated as compared to the normoxic culture. This effect was paralleled by a significantly reduced cell damage or cell death under hypoxic conditions as evaluated by the cellular release of LDH whereby the measurement of caspase 3/7 activity revealed little if any differences in apoptotic cell death between the various cultures. The MSC culture under hypoxic conditions was associated with the induction of hypoxia-inducing factor-alpha (HIF-1 alpha) and an elevated expression of energy metabolism-associated genes including GLUT-1, LDH and PDK1. Concomitantly, a significantly enhanced glucose consumption and a corresponding lactate production could be observed in the hypoxic MSC cultures suggesting an altered metabolism of these human stem cells within the hypoxic environment.

Identificador

http://dx.doi.org/10.15488/462

http://www.repo.uni-hannover.de/handle/123456789/485

Idioma(s)

eng

Publicador

London : Biomed Central Ltd

Relação

http://dx.doi.org/10.1186/1478-811X-8-18

ISSN:1478-811X

Direitos

CC-BY 2.0

https://creativecommons.org/licenses/by/2.0/

frei zugänglich

Fonte

Cell communication and signaling 8 (2010)

Palavras-Chave #adipose-tissue #bone-marrow #oxygen concentration #reactive oxygen #metabolism #growth #consumption #responses #damage #dna #ddc:500
Tipo

status-type:publishedVersion

doc-type:article

doc-type:Text