To the Editor:
Mesenchymal stem cells (MSCs) are stromal cells that were originally
reported in the bone marrow (BM) but can be isolated from various other
tissues. MCSs can differentiate into multiple mesodermal cell lineages
[1].
BM-MSCs are used in numerous clinical applications including
regenerative medicine [2]. Since MSCs are a rare cell population in
the bone marrow, one should expand these cells for clinical
applications. It is generally believed that reduced oxygen tension byin vivo transplantation plays a critical role in the success of
implantation, and more specifically, cell survival and expansion
[3]. However, BM-MSCs are shown to have excellent expansion when
grown in hypoxic conditions [4]. This observation, indeed, questions
the common belief on the importance of oxygen treatment for BM-MSC
proliferation [5,6].
To check whether oxygen or glucose supplementation is the most important
factor in BM-MSC expansion, we used our previously published
context-specific metabolic network model of these cells [7]. At
three different oxygen-uptake rates, which can represent normoxia,
physoxia and hypoxia, we computed cell growth rate as a function of
glucose uptake rate.
To be specific, we used flux balance analysis (FBA) approach to simulate
the cell growth at different oxygen and glucose consumption rates
[8,9]. To this end, we assumed that all nutrients are available in
excess, which, in our constraint-based model, translates to unbound
uptake fluxes. Then, at three different oxygen-uptake flux values
(i.e. , 0.1, 4, and 24), we used FBA to compute the maximum
possible biomass production rate as a function of glucose uptake rate.
In FBA-based simulations of metabolism, biomass production rate is
typically considered as the objective function for modeling cell
expansion and proliferation.
The results of our analysis are summarized in Figure 1. In this plot,
Interestingly, one can observe that the three simulations result in
almost similar growth patterns. Therefore, our model suggests that
oxygen has only a minor influence on the proliferation of BM-MSCs. On
the other hand, glucose uptake rate considerably changes the growth
rate. On the other hand, the glucose uptake rate considerably changes
the growth rate, which is in line with the recently published
observations [8].
Here, we used a constraint-based model of BM-MSCs to investigate the
effect of oxygen and glucose on the metabolism of these cells. Our
results suggest that for cell expansion, glucose availability is more
important compared to oxygen availability. In our simulations, possible
oxygen-dependent gene regulation is ignored, i.e. , the same
metabolic network model is used at all oxygen uptake rates. However,
based on the recent observation that protein expression in MSCs is not
affected by oxygen decrease, this assumption is acceptable [4]. One
should note that, to a great extent, BM-MSCs rely on glycolytic
metabolism, which limits the effect of oxygen. Consequently,
availability of glucose to these cells seems to be a critically
important factor.
Many tissue engineering studies have considered oxygen-releasing
scaffolds for improving cell survival and proliferation postimplantation
[9]. We want to emphasize here that for a successful tissue
engineering practice, glucose-releasing scaffolds might also be a
neglected necessity.