Background
Ageing is the consequence of an accumulation of physiological changes over time, eventually increasing the mortality risk. Because ageing is the major risk factor for reduced wellbeing and for the most common human diseases of Western societies, treatment of elderly patients may be improved by understanding their biological age, the rate at which a person ages, and health status, rather than simply chronological age.
Many potential biomarkers of biological age have been suggested and are being tested for their association with chronological age, disease and prospective mortality [
1]. In a search for new transcriptomic biomarkers of ageing, we found that the expression of 1853 genes in blood was associated with chronological age. Of these, 244 were associated with familial longevity, i.e. they were differentially expressed in middle-aged offspring of nonagenarian siblings as compared with controls from the Leiden Longevity Study (LLS). A low expression level of one of these 244 genes, the interleukin 7 (IL7) receptor (
IL7R), associated with a better metabolic health profile [
2]. Hence,
IL7R gene expression in blood seems a good candidate biomarker for healthy ageing.
IL7R is important for the body’s innate and adaptive immune responses and plays a role in regulating development, differentiation and survival of T cells [
3,
4]. IL7R is required for IL7 signalling, which in mice has been shown to be crucial for early T cell development, as well as for homeostasis of naïve and memory CD8+ T cells [
5,
6]. Previously, we observed that the offspring of nonagenarian siblings avoid the usual age-related reduction of percentages and numbers of naïve T cells in the periphery [
7]. Reduction of proinflammatory IL7 signalling may contribute to this better retention of naïve T cells and may thereby influence the biological age and health status of elderly individuals, given that possessing a fuller naive T cell repertoire would be expected to better protect against pathogens to which the individual has not been previously exposed.
To explore whether the expression profiles of other genes in the close vicinity of
IL7R may exhibit even better ageing biomarker properties, we first identified the six interaction partners of
IL7R using the STRING protein-protein-interaction database (
http://string-db.org/). Next, gene expression levels of all seven genes in the
IL7R gene network were measured in 87 nonagenarians who also had a nonagenarian sibling, 337 of their offspring, considered ‘healthy agers’, and 321 controls from the LLS. We tested whether the level of expression of the
IL7R network genes associated with chronological age by comparing the nonagenarians with the middle-aged controls. Differential expression in this comparison may be explained by the age difference between these groups, early environmental factors or the longevity trait in these nonagenarians, which is not present in controls.
To further investigate whether the expression of the age-associated genes also associates with biological age and disease prevalence, we compared the offspring of the nonagenarians, representing individuals with a lower biological age, as marked by lower prevalence of age-related disease and beneficial metabolic profiles [
8,
9], with similarly aged controls. Additionally, we explored whether the expression of the IL7R interaction partners is associated with common immune-related diseases in middle-aged individuals. Finally, we performed survival analysis in the nonagenarians and the combined group of middle-aged offspring and controls to determine the relationship between expression of these genes and mortality.
Discussion
In this paper we made two opposing observations. First, relative to controls, ‘healthy agers’, i.e. nonagenarian siblings and their offspring, were characterized by reduced IL7R expression in blood and increased IL7R expression in middle age is associated with higher prevalence of immune-related diseases. Second, since gene expression levels of IL7R decreases with chronological age, higher IL7R expression levels may indicate a more ‘youthful profile’ and thus better health, which was supported by the observation that higher IL7R gene expression levels, in both the nonagenarians and middle-aged individuals, associate with better prospective survival. The mechanism underlying these observations requires further investigation to determine whether regulation of IL7R gene expression has a causal role as determinant of the rate of ageing.
The notion that low
IL7R expression levels are beneficial for reaching old age healthily corresponds with previous observations that autoimmune disease patients express increased levels of the IL receptor/ligand complex genes [
12,
13,
15] and that antagonizing IL7 or IL7R may offer possible treatment [
12,
14]. An increase in systemic inflammation has generally been reported with increasing age, so-called 'inflamm-ageing' [
17]. Long-lived individuals, such as LLS nonagenarians, can be seen as ‘slow’ or ‘healthy agers’ who do not show the commonly observed age-related characteristics of 'immunosenescence' and display relatively low levels of proinflammatory markers [
7]. Our results may suggest that nonagenarian members of long-lived families have more efficient IL7 signalling, since they seem to require less compensation because of their remaining naïve T cell population, resulting in greater reserve capacity to cope with infections in old age. On the other hand, very low IL7R signaling has been observed in severe combined immunodeficiency [
18] and in HIV infection [
19,
20]. Based on this, we conclude that, besides the troublesome effect of the absence of IL7 signalling, a somewhat lower baseline level of
IL7R gene expression, and potentially IL7 signalling, may contribute to healthy ageing.
Despite these observations, the expression of the
IL7R gene network was negatively correlated with age, suggesting that low expression levels correlate with decreased health, which is consistent with our observation that low
IL7R gene expression associates with higher prospective mortality. Clearly, this finding is inconsistent with the observation that, in the same group of individuals, low
IL7R gene expression level is associated with familial longevity and a lower prevalence of immune-related disease. A similar paradox has been found in PBMCs, where a lower frequency of naïve T cells (and a higher frequency of differentiated T cells) was associated with better survival in elderly individuals, while a higher frequency was found in offspring of nonagenarians compared to the controls, suggesting an association with lower biological age [
7,
21]. This might be interpreted as follows; if the individual is able to counter the reduction of
IL7R gene expression with age by keeping the level of differentiated T cells high as memory cells to control disease, this may be associated with healthy old age.
Contributing to the paradox, may be the fact that there are two forms of IL7R exerting different functions, membrane-bound and soluble IL7R. Membrane-bound IL7R, also known as lymphocyte surface marker CD127, may transduce IL7 signalling, while soluble IL7R may represent a negative compensatory mechanism regulating IL7 signalling [
19,
22,
23]. Because we used the recommended Taqman assay for the measurement of
IL7R gene expression that cannot distinguish between the
IL7R splice forms, we are unable to interpret how IL7 signalling is affected by the gene expression changes.
IL7R gene expression levels and CD127 did not correlate in the offspring or controls and CD127 did not show a difference between the two groups. The absence of correlation between
IL7R gene expression levels and CD127 may be explained by the difference in cellular composition of whole blood and PBMCs, i.e. PBMCs do not contain basophils and eosinophils. However, a study by McKay and colleagues suggests that PBMCs are the main source for
IL7R gene expression levels in whole blood [
24]. In addition, adjustment for the different white blood cell counts results in similar associations in our whole blood gene expression analysis of
IL7R (Additional file
1: Table S1), indicating that the white blood cell composition has limited effect on the expression of
IL7R in our study. Although soluble IL7R has been shown to potentiate IL7 signalling [
25], our results might suggest that the decrease in
IL7R gene expression reflects mainly a decrease in the mRNA coding for soluble IL7R, resulting in more efficient IL7 signalling.
We showed that
IL7R gene expression in blood is associated with immune-related disease. Previous meta-analysis and genome-wide association studies showed that genetic variation in the
IL7R gene is associated with ulcerative colitis [
26], multiple sclerosis [
27‐
29], primary biliary cirrhosis [
30] and type 1 diabetes [
31]. These results may suggest that genetic variation in and the expression of the
IL7R gene is involved in auto-immune and chronic inflammatory disease. Hence, optimal response of the immune system may contribute to human longevity.
Further evidence that IL7 signalling may contribute to biological ageing and longevity is that it is closely connected to mTOR signalling, a pathway known for its effects on lifespan in animal models, which has recently also been implicated in human ageing and longevity [
32,
33]. Several studies in mice provided evidence for the connection between IL7 and mTOR signalling. IL7 induces phosphorylation of the mTOR complex 1 (mTORC1) downstream targets S6 and 4EBP1, an effect antagonized by the mTOR inhibitor rapamycin. The reverse may occur as well; rapamycin inhibits proliferation and induces apoptosis of pre-B acute lymphoblastic leukemia and these effects are abrogated by IL7 [
34]. Functional studies have validated
IL7R as a FoxO1 target gene [
35]. Acute deletion of FoxO1 induced a rapid and profound downregulation of
IL7R expression, which is associated with a significant reduction of
IL7R mRNA [
36]. In addition, cytokine stimulation (including IL7) induces FoxO1 phosphorylation and decreased transcription of target genes [
36]. In B cells, it has been shown that the mTOR complex 2 (mTORC2) suppresses
IL7R gene expression by regulating FoxO1 phosphorylation [
37]. Taken together, decreased IL7 levels and decreased mTORC1 activity seem to go hand-in-hand, further implying that decreased IL7 levels are beneficial, since decreased mTORC1 increases lifespan. The same is true for decreased IL7R and increased mTORC2, the latter we have recently shown to be associated with human longevity [
33]. Gene expression levels of several of the mTOR-related genes, including
RPTOR,
FOXO1 and
MTOR, are indeed positively and significantly correlated with
IL7R expression in the LLS (data not shown). Considering the clear connections with IL7 signalling and similar findings on the level of gene expression variations, mTOR signalling might also be involved in “inflamm-ageing” as part of its lifespan-regulating effect.
In a previous studies of the LLS population, Dekker and colleagues found more apoptotic activity and less senescence in the cultured skin fibroblasts of the offspring as compared to controls [
38]. In addition, flow cytometric analysis in HIV-infected individuals demonstrated that CD8+ cells expressing high levels of
IL7R also expressed slightly higher levels of anti-apoptotic markers, whereas nearly all apoptotic cells had low levels of
IL7R [
39]. Our finding of decreased
IL7R expression in members of long-lived families fits well with these previous results.
Methods
Study population
Leiden Longevity Study
The individuals investigated in this study are participants of the LLS. The families participating in this study have at least two siblings with a minimum age for men of 89 years and for women of 91 years [
40]. The offspring of these long-lived individuals were also included and, because they have an increased chance of becoming long-lived (30 % reduced standardized mortality rate) and a lower prevalence of age-related disease [
9], we consider them ‘healthy agers’. In addition, the partners of the offspring, which are similarly aged and are subjected to the same environmental exposures, were included as population controls. Blood samples were taken from all the participants. The LLS was approved by the Medical Ethical Committee of the Leiden University Medical Center and all participants gave written informed consent.
Sample collection and RNA preparation
For the current study, we selected 87 unrelated nonagenarians, 337 offspring and 321 partners belonging to 281 nuclear families (Table
1). These samples were randomly selected, but in such a way that age and gender were balanced between the groups and the age range was as large as possible. Only individuals without outlying cell counts (>3 SD below or above the standard error of the mean) were included. This subpopulation is representative for the whole LLS regarding disease prevalence and parameters involved in metabolic syndrome [
9,
41]. From these non-fasted individuals, peripheral blood was harvested using PAXgeneTM tubes (Qiagen, Venlo, The Netherlands). The tubes were frozen and kept at −20 °C for ~3–5 years. After thawing at room temperature for at least 2 h, total RNA was extracted from the approximately 2.5 ml of peripheral blood in each tube following the manufacturer’s recommended protocol (PAXgene Blood RNA Kit Handbook, Qiagen, Venlo, The Netherlands). The quality and integrity of the total RNA was evaluated on the 2100 Bioanalyzer (Agilent Technologies, Amstelveen, The Netherlands) and the concentration was measured using a NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA). Quality criteria included a 28S/18S ratio, as measured by the 2100 Bioanalyzer, of at least 1.2, and a total RNA yield of at least 3 μg.
RT-qPCR
For all seven IL7R network genes the suggested Taqman® assay (Applied Biosystems, Bleiswijk, the Netherlands) was selected. Reverse transcription was performed with total RNA from blood of the 745 samples that passed QC using the First Strand cDNA Synthesis Kit, according to the manufacturer’s protocol (Roche Applied Science, Almere, the Netherlands). cDNA was amplified using the DNA Engine Tetrad® 2 Peltier Thermal Cycler (Bio-Rad, Veenendaal, The Netherlands). qPCR was then performed with the Taqman® method using the BiomarkTM 48.48 and 96.96 Dynamic Arrays (Fluidigm Amsterdam, The Netherlands). Relative gene expression of the BioMark™ Array data were calculated by using the 2
−ΔΔCt method, in which Ct indicates cycle threshold, the fractional cycle number where the fluorescent signal reaches the detection threshold [
42].
YKT6 was used as internal control and commercially available human total reference RNA (Clontech Laboratories, Mountain View, CA, USA) as reference RNA.
White blood cell subtypes
In the whole blood samples of the participants the following white blood cell subtypes were counted using the automated Siemens ADVIA 1200 system (SMSD, Tarrytown, NY) in the Leiden Medical Diagnostics Center: leukocytes, thrombocytes, neutrophils, lymphocytes, monocytes, basophils and eosinophils.
CD127 staining
Cryopreserved PBMCs were thawed and treated with human immunoglobulin (GAMUNEX; TalecrisBiotherapeuthics) and ethidium monoazide (EMA, Invitrogen) to block Fc receptors and stain dead cells followed by indirect staining for CD3 using an OKT3 supernatant and a Pacific Orange-conjugated anti-mouse IgG (Invitrogen). After blocking unbound secondary antibodies with mouse serum (Chemicon, Millipore), cells were surface-stained with CD4-Pacific Blue, CD127-Alexa Fluor 647 (BioLegend, San Diego, USA) and CD8-PerCP (BD Biosciences, Heidelberg, Germany). Cells were measured immediately using an LSR-II (BD).
For data analysis, EMA+ dead cells were excluded and lymphocytes were gated using an FSC vs. SSC dot plot based on their size and granularity. T cells and non-T cells were characterized as CD3+ and CD3− cells within the lymphocyte gate. In the CD3+ gate, CD4 and CD8 cells were characterized in a CD4 vs. CD8 dot plot as CD4 + CD8− and CD4−CD8+ cells, respectively. The mean fluorescence intensity (MFI) of Alexa-Fluor647 (CD127) was determined on total lymphocytes, CD3−, CD3+, CD4+ and CD8+ cells. To standardize for fluctuation of the instrument over the measurement period of a few weeks, MFI of each studied population was standardized against the MFI of an unstained control PBMC for each experimental day, by dividing the MFI of each population by that of the cells in the lymphocyte gate of the unstained control. Flow cytometry data analysis was performed using FlowJo software (Tristar, San Diego, USA).
Statistical analysis
Geneset analysis of gene expression data
The Globaltest methodology was designed to determine whether the common expression pattern of genes within a pre-defined set is significantly related to clinical outcome [
10,
11]. A generalized linear model is used to estimate a ‘Q-statistic’ for each gene set, which describes the correlation between gene expression profiles, X, and clinical outcomes, Y. The Q-statistic for a gene set is the average of the Q-statistics for each gene in the set. The Globaltest method was used to perform geneset analysis comparing two groups of individuals (either nonagenarians vs. controls or offspring vs. controls) including age (in offspring vs. controls only), gender and their interaction as covariates. The globaltest R package [
43] has been used to perform analyses.
Single gene analysis of gene expression data
Differences in expression level between nonagenarians, their offspring and controls were assessed using linear regression. In these analyses, the expression level was the dependent variable and the two groups of individuals (either nonagenarians vs. controls or offspring vs. controls) were included in the model as a categorical variable together with age (in offspring vs. controls only), gender and their interaction as covariates. To take into account dependencies within sibships, robust standard errors were used, i.e. the variance was computed from the between family variation. The P-values were also based on these robust standard errors. Analyses were performed using the software package STATA/SE 11.0 (DPC Software, StataCorp 2009).
To further investigate the candidate genes, their expression level was associated with white blood cell counts. Subsequently, we adjusted both the comparison between nonagenarians and controls and between offspring and controls for each of these cell counts separately.
Association of gene expression with immune-related diseases
Information on medical history was requested from the participants’ general practitioners. Gene expression of IL7R and IL7 was associated with prevalence of T2D, COPD and RA and the sum score of these diseases. The linear regression model with IL7R/IL7 gene expression levels as outcome was adjusted for age, gender and their interaction. The sum score indicates the number of patients with T2D, COPD, RA or a combination thereof. Next, the comparison of IL7R and IL7 gene expression between offspring and controls was adjusted for the prevalence of these diseases, using the linear regression model described above.
Prospective analyses
Prospective analyses of IL7R-related genes was performed with 81 nonagenarians and the combined group of 313 offspring and 306 controls. After a mean follow-up time of 7.40 (nonagenarians) and 6.15 years (offspring and controls), 82.7 % (N = 67, nonagenarians) and 6.5 % (N = 40, offspring and controls) of the individuals had died. Prospective analyses were performed using a left-truncated Cox proportional hazards model, to adjust for late entry into the dataset according to age. Age at inclusion, gender, their interaction (middle-age only), group (offspring or partner) and white blood cell counts were included as covariates. To take into account dependencies within sibships, robust standard errors were used, i.e. the variance was computed from the between family variation. The P-values were also based on these robust standard errors. Analyses were performed using the software package STATA/SE 11.0 (DPC Software, StataCorp 2009).
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
ABM, RvdB, DvH, ED, GP, G-JBvO and PES were involved in data acquisition. WMP, EBvdA and JD performed statistical analyses. WMP, EBvdA, JD, RJ, ST, MB interpreted the data. PES and MB were responsible for the study concept and design. WMP, PES and MB drafted the manuscript. All authors read and approved the final manuscript.