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Curr Opin Chem Biol. Author manuscript; available in PMC Dec 1, 2010.
Published in final edited form as:
PMCID: PMC2975492
NIHMSID: NIHMS164480

Non-genetic cell-to-cell variability and the consequences for pharmacology

Summary

Recent advances in single-cell assays have focused attention on the fact that even members of a genetically identical group of cells or organisms in identical environments can exhibit variability in drug sensitivity, cellular response, and phenotype. Underlying much of this variability is stochasticity in gene expression, which can produce unique proteomes even in genetically identical cells. Here we discuss the consequences of non-genetic cell-to-cell variability in the cellular response to drugs and its potential impact for treatment of human disease.

Introduction

It has long been recognized that differences from one cell to the next can arise through variation in the extracellular environment (e.g. morphogen gradients during embryogenesis) or from genomic alteration (e.g. genetic heterogeneity within a tumor). Only recently has it become clear that intracellular biochemical fluctuations can also have profound effects on phenotype. These fluctuations cause genetically identical cells to vary significantly in their responsiveness to stimuli and drugs even in a uniform environment [1,2**,3**,4,5*,6,7**,8*]. Such cell-to-cell differences arise from stochasticity in the biochemical reactions. Gene expression is one of the best understood of these stochastic processes (see Box 1), but cytoskeletal rearrangement, protein localization, post-translational modification and formation of protein complexes are almost certainly also involved in generating variability. The net result is the creation of cell populations with the same genome but unique proteomes.

Box 1. Stochastic gene expression

An early and influential experiment analyzed the sources of noise in gene expression by tagging two copies of the same promoter with two different fluorescent proteins in E. coli [46]. The authors found that both “extrinsic noise” (affecting both gene copies equally, but varying from cell to cell) and “intrinsic noise” (caused by the inherent stochasticity in transcription and translation, and random between gene copies) contributed to cell-to-cell variability. This intrinsic noise arises in bacteria because proteins are produced in translational bursts from mRNA transcripts [47] and because mRNA molecules themselves are produced in transcriptional bursts [13]. In mammalian cells, however, transcription plays a more dominant role. Work in Chinese hamster ovary cells showed that transcriptional bursts are infrequent but long-lasting, caused by random transitions between inactive and active states of genes. These bursts produce high variation from cell to cell in mRNA levels and consequently in protein number [48*].

Network architecture has significant impact on noise propagation in complex signaling systems. Noise in upstream regulators can propagate to downstream genes, thus adding to the intrinsic noise in the gene’s output [49]. Negative feedback can reduce the effects of noise by compensating for deviations from a set point [50], while positive feedback can have the opposite effect, amplifying small fluctuations. Cooperativity helps to maintain a state, buffering it against small fluctuations, and providing a long-term protein-level memory [51].

Transient heritability is an interesting property of phenotypic variability arising from cell-to-cell differences at the proteome level [5*,9*,10**]. While genetic differences are stably passed on to progeny and epigenetic modifications are heritable for 10–105 cell divisions [11], the state of the proteome is heritable on a much shorter timescale (one to a few divisions) [5*,9*,10**]. The proteomes of recently born sister cells are similar, owing to binomial partitioning of abundant cellular components during cell division [12,13]. The phenotypes of sister cells are therefore more similar than those of two cells chosen at random, although stochastic fluctuations cause sister cells to decorrelate rapidly [5*,8*,10**].

The timescales and mechanisms underlying stochastic, epigenetic, and genetic variation are distinct, but the three types of variation interact (Figure 1a). Most obviously, genetic and epigenetic factors determine the mean levels or activities of proteins, and stochastic processes determine dispersion around the mean. However, the proteome also influences epigenetic regulation of gene expression [14,15] and it has been suggested that the expression levels of certain proteins influence the probability that mutations will be fixed [16].

Figure 1
Cell-to-cell variability of the proteome gives rise to phenotypic heterogeneity

The distribution of protein abundance and resulting variability in phenotype

When the effects of cell size are taken into account, the concentration distribution for many proteins across a clonal population of mammalian cells is well-fit by a log-normal distribution [2**,5*], with a coefficient of variation (CV, equal to the standard deviation divided by the mean) of ~0.1 to ~0.6 [2**,5*,10**]. Log-normal distributions are long-tailed so that even a tight distribution (CV=0.25) contains cells in the 95th percentile that have 2.5 times the abundance of a particular protein than cells in 5th percentile, and this spread increases dramatically with increasing CV (Figure 1b). Some distributions are even bimodal, with potentially dramatic effects on cell fate [17*]. It is not known why distributions differ [2**,10**,1820] but regulatory processes may be involved [19,20]. In mammalian cells, the relative levels of most proteins do not appear to be highly correlated [10**], although correlation is observed in the case of cell cycle regulated genes [18]. Based on current observations, uncorrelated, long-tailed distributions in protein abundance should be considered the default state; deviations from this probably reflect the operation of active processes that affect variability (feedback control on transcription, for example).

We are accustomed to thinking about phenotypes as discrete states in which a single genotype maps to a distinct phenotype. However, the existence of a unique proteome in each cell means that a single genotype can give rise to a range of phenotypes, with varying degrees of overlap (Figure 1c). Whether the phenotypic range is wide or narrow cannot easily be predicted a priori. For example, in the case of receptor-mediated apoptosis, the time between ligand exposure and the commitment to death is very variable from one cell to the next but the time between commitment to apoptosis and completion of caspase-mediated cell killing is not [5*,2123]. Is phenotypic variation from one cell to the next simply the inevitable consequence of building pathways from imprecise components (proteins that vary in abundance, for example) or might it actually have adaptive advantage? It has been proposed that intrinsic variability in otherwise identical lymphocytes is necessary for correct operation of the adaptive immune response [24].

In general, the connection between the levels of a set of interacting proteins and a phenotype depends on the precise biochemistry of the regulatory process. This is true for the mean levels of a protein (determined genetically) and for fluctuations around the mean. We can approximate the relationship between a protein’s level and a cellular response by a transfer function. The phenotype distribution across a population thus depends on both the heterogeneous protein distribution and the complexity of the transfer function (Figure 1d). In some cases, the function is linear, at least over a limited range, but nonlinear, non-monotonic relationships and thresholds are likely more common [1,25]. Moreover, while some phenotypes are influenced primarily by a single protein [7**,9*], most are controlled by multiple factors [2**,5*,26,27], so intuiting cellular phenotype from unique proteomes is not trivial. Therefore, understanding phenotype at a quantitative level requires methods for measuring variation (see below) and development of modeling frameworks that are able to account both for variation in the proteome and the complexity of transfer functions that determine phenotype (see Box 2).

Box 2. Modeling cell-to-cell variability

The amount and detail of information available about a biochemical process and the goals of the analysis determine how cell-to-cell variability should be modeled. The simplest models are conceptual or diagrammatic and attempt to account for the mean values of key variables (e.g. rates of physiological processes) and their dispersion about the mean [3**]. More rigorous are methods based on stochastic differential equations (SDEs) or the Langevin approach in which the biochemical reactions are cast as deterministic differential equations with an added noise term [49]. Finally, the chemical master equation, which describes the probability that individual molecules will collide and react in a given time interval, can be approximated numerically using the Stochastic Simulation Algorithm (SSA) or Gillespie Algorithm [52].

If the goal is to study the stochastic process in detail, then use of SDEs or the SSA is necessary, but it is also possible to separate the causes and consequences of stochasticity. For example, if we want to understand cell-to-cell variability in phenotype arising from differences in the levels of relatively abundant proteins, then we can combine deterministic models with distributions of initial protein concentrations and arrive at reasonable and useful approximations. The processes that generate the distribution in parameter values are stochastic, but given a measured or assumed distribution at the outset of the simulation, we can then use deterministic differential equations. This greatly facilitates parameter estimation, simulation, and model interpretation. Using such a hybrid approach merely awaits the development of a practical implementation of the modeling methodology.

Measuring cell-to-cell variation

Linking protein expression levels to phenotype is most commonly performed using fixed and live-cell microscopy. Only a limited number of cellular events are visible using bright field or phase-contrast illumination (e.g. changes in cell size, morphology, motility, cell division) and fluorescent biosensors are needed to assay specific biochemical processes. Cell permeable dyes, such as JC-1 used to measure changes in mitochondrial membrane potential during apoptosis, can simply be added to cell growth media, while genetically encoded reporters have to be actively inserted into cells. When expressed in cells, activity-sensitive fluorescent biosensors can report on protein-protein association [28], protein conformation [29], protein cleavage [1], and protein modifications [30]. The ectopic expression of fluorescently tagged proteins has also been used to monitor changes in protein subcellular localization [31], protein expression and degradation [8*], and changes in cell cycle phase [32]. One challenge with these reporters is that expressing them in cells can perturb the phenomena under study. To minimize this, fluorescent reporters can be fused to genes at their normal genomic loci, so that native promoters are retained [10**,19,20,33]. Libraries of such cell lines have been used to correlate protein levels and localization in drug-treated cells with cell fate [7**].

Immunofluorescence-based assays such as flow cytometry [6,34] and high-throughput immunofluorescence microscopy [35,36] have the advantage that no reporters are required, and all assays can be carried out in unaltered cells, often allowing for the transition of an established assay into new cell lines or even primary tissue samples. However, these assays do not provide information on temporal dynamics and are limited by the availability of specific antibodies. Ultimately, we would like to obtain data on the complete proteomes of single cells, but this is not feasible using current technology. High-dimensional flow cytometry [37,38], improved microdissection [39] and high-sensitivity mass spectrometry [40] may make systematic characterization of proteomes at the single-cell level possible. Until then, the obvious approach is to measure protein distributions by flow cytometry and phenotypes by live-cell microscopy.

Potential implications of cell-to-cell variability in pharmacology and human disease

How might emerging understanding of non-genetic cell-to-cell variability impact pharmacology and the treatment of human disease? A significant problem in cancer is fractional killing or incomplete growth inhibition of tumor cells [41]. Multiple explanations of fractional killing have been proposed including variation in the access of tumor cells to a drug, genetic heterogeneity, drug insensitivity during certain cell cycle phases [42,43] and, most recently the presence of drug-resistant cancer stem cells [44]. However, natural fluctuations in the proteome and resulting dispersion in drug responsiveness of cells [3**,4,5*,7**] is likely to be an important but poorly appreciated factor. For example, protein expression outliers in key stem cell markers such as Nanog and Sca-1 have been shown to influence pluripotency and can remix to repopulate the full distribution of expression levels [9*,17*]. Similarly, drug-resistant cancer stem cells, rather than being a static genetically or epigenetically distinct subfraction, may represent population outliers resulting from proteomic heterogeneity.

If proteomic fluctuations indeed play a critical role in drug sensitivity, new approaches to maximizing therapeutic efficacy may be required. Fractional killing is often combated by dosing patients repeatedly with the idea that cells that are resistant to the first round of therapy will be killed in the second round, perhaps because they are in a different cell cycle phase [42,43]. However, if fluctuations in the proteome play a significant role in fractional killing, then repeat treatment may not work because outliers in the dose-response profile will survive to repopulate the full distribution [5*,10**,45]. Nevertheless, it may be possible to identify compounds that alter the distribution of proteome states so as to reduce the fraction of non-responders. Combination therapy is standard in cancer care, but targeting the dispersion of phenotypic responses has not, to our knowledge, been examined as a strategy. Preliminary data suggests it might work however, since heterogeneity in the responses of cells to drugs such as a death ligand can be altered by changing the expression levels of apoptotic regulators [5*]. The way forward would appear to involve understanding which proteins contribute most to variability in response to a particular drug and then attempting to target these proteins.

In many cases, the phenotypic heterogeneity within a population is not simply a binary choice between death and survival. For example, cells treated with microtubule poisons such as nocodazole can respond with as many as seven distinct phenotypes [3**]. Thus, following exposure to a drug, even a relatively homogeneous population of cells can become significantly more diverse. This induced phenotypic heterogeneity is likely to be even more complicated when multiple drugs are employed, especially if one drug causes permanent genomic changes. As a consequence, it is exceedingly difficult to predict the optimal treatment regimen with the large number of chemotherapeutics employed at this time.

Conclusions

The complexity of cellular response to drugs suggests that it will be valuable to study pre-clinical pharmacology using sophisticated single-cell measurement of both mean behaviors and variation about the mean in proteome and phenotype. While the phenomena of stochastic gene expression, proteome fluctuations and cell-to-cell variability in phenotypes have clearly been established in the context of single-celled organisms and cell lines, the full impact on pharmacology and the treatment of human disease is currently unknown. These concepts may actually be clinically applicable in the short term, as relevant single cell data is already being collected in pharmacological screens, histopathology samples, and flow cytometry analysis of blood. Advances in mathematical modeling methods are also required to account for stochastic biochemical processes, dispersion in model parameters, and the impact on phenotype. Nonetheless, there is every reason to believe that non-genetic variability in the proteome will be recognized, alongside genetic changes and local environment, as an important factor in the development and treatment of human disease.

Acknowledgements

This work was supported by National Institute of Health (NIH grants) GM68762 and CA112967.

Footnotes

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