Dynamics of adipose tissue turnover in human metabolic health and disease
White adipose tissue is a highly plastic organ and is an important regulator of whole-body metabolism and energy balance. The magnitude of adipose tissue mass is determined by dynamic changes in the synthesis and breakdown (i.e. turnover) of adipocytes and triacylglycerols (TGs). Obesity is a disorder characterised by excessive adiposity and is a risk factor for diseases, including the metabolic syndrome and type 2 diabetes. Adipose tissue expansion is necessary to accommodate chronic excess energy intake and is characterised by enlargement of existing adipocytes (hypertrophy) and by increase in pre-adipocyte and adipocyte numbers (hyperplasia). Evidence suggests that the manner of subcutaneous adipose expansion can influence metabolic health, as impaired adipogenesis, namely restricted hyperplasia, may lead to ectopic lipid deposition in the liver and skeletal muscle, contributing to the pathogenesis of obesity-related disorders. Despite the plausible role of adipose turnover in human health and pathology, little is known about the in vivo kinetics of adipose tissue components (both adipose cells and TGs). This is due, in part, to the slow turnover rate of adipose tissue and the complexity of directly labelling pathway precursors. This review provides a brief summary of findings derived from in vitro techniques, as well as an overview of two in vivo methods that are being implemented to assess the turnover of adipose cells and TGs. Finally, the role of adipose tissue turnover in metabolic health and disease is discussed.
KeywordsAdipocyte Adipocyte death Adipose kinetics Adipose lipid turnover Adipose tissue Metabolic disease Metabolic health Obesity Review Triacylglycerol
Brown adipose tissue
Mass isotopomer distribution analysis
Visceral adipose tissue
White adipose tissue
Adipose tissue is an essential organ and is the primary site for energy storage as triacylglycerols (TGs). White adipose tissue (WAT) and brown adipose tissue (BAT) are the predominant types in mammals. As WAT and BAT have different developmental origins and the majority of human adipose tissue is WAT, this type will be the focus of this review. Traditionally, studies of WAT function have revolved around its significant role in controlling energy homeostasis by storing and releasing lipids in response to energy demands. However, WAT has additional properties, including secretory functions (release of adipokines), that affect insulin sensitivity and metabolic homeostasis, contributing to the pathogenesis of obesity and related comorbidities .
WAT is distributed throughout the body in several depots, each with distinct functions. Evidence suggests that regional distribution of WAT, rather than overall obesity, may be a stronger predictor of metabolic health risks. The accumulation of fat in the upper body (namely visceral adipose tissue [VAT] but also subcutaneous abdominal [scABD]) confers a higher risk of developing type 2 diabetes mellitus and cardiovascular disease, while in the lower body, subcutaneous gluteal and subcutaneous femoral (scFEM) fat may be metabolically protective . Sexual dimorphism in fat distribution is also well-documented: women, despite having, on average, a higher percentage of body fat than men, display preferential adipose accumulation in the ‘protective’ lower-body depots . Conversely, men tend to deposit more fat in the upper-body VAT depot . Sex differences in fat distribution and the distinct functions of adipose depots have been discussed in previous reviews [5, 6].
Although most adipose growth occurs during childhood and adolescence, WAT retains the ability to expand during adulthood in response to fluctuations in energy balance. The magnitude of adiposity during the development of obesity is determined by dynamic changes in the synthesis and removal (i.e. turnover) of adipose cells (pre-adipocytes and adipocytes) and TGs. Despite the negative health consequences associated with obesity, little is known about in vivo WAT turnover in humans. This review provides a brief summary of findings obtained from in vitro methods, as well as an overview of two in vivo approaches that are being implemented to assess the turnover of adipose cells and TGs. Finally, the role of WAT turnover in metabolic health and disease is discussed.
WAT stores energy in the form of TGs and releases fatty acids via lipolysis to maintain metabolic homeostasis. To accommodate lipids, adipose expansion occurs via the enlargement of existing adipocytes (hypertrophy) and/or the proliferation and differentiation of pre-adipocytes to adipocytes (hyperplasia or adipogenesis). Evidence suggests that the manner of subcutaneous WAT expansion (hypertrophy vs hyperplasia) in humans can influence cardiometabolic health. Cross-sectional and longitudinal studies have shown that hypertrophic abdominal adipocytes are associated with insulin resistance [7, 8] and type 2 diabetes [9, 10], independent of overall obesity. It has also been proposed that impaired adipogenesis, or restricted hyperplasia, may lead to ectopic fat deposition in the liver and skeletal muscle, contributing to the pathogenesis of obesity-related disorders . Arner et al developed an ‘adipocyte morphology value’, defined as the difference between the measured adipocyte size and the expected size given the curve-linear fit for a given body mass, to predict scABD cellularity in humans . These authors reported that greater scABD hypertrophy (i.e. higher morphology index) was linked to insulin resistance and lower adipocyte number, independent of sex and adiposity, while greater hyperplastic expansion was associated with better insulin sensitivity. Collectively, the above-mentioned data support the ‘adipose tissue expandability hypothesis’, which postulates that a lack of hyperplasia, coupled with a high prevalence of hypertrophic adipocytes, results in a limited capacity of WAT to expand and store fat, thus causing impaired metabolic health .
However, the role of adipogenesis (i.e. hyperplasia) in health risks is debatable. Recent observations reported a higher prevalence of small fat cells in insulin-resistant individuals and in those with type 2 diabetes, compared with healthy individuals, suggesting hyperplastic expansion [8, 14, 15, 16]. Importantly, we showed that 8 weeks of 40% overfeeding (~7.6 kg weight gain) resulted in greater impairment of insulin sensitivity in individuals who had smaller adipocytes at baseline compared with those who had larger adipocytes . Another human overfeeding study demonstrated that smaller adipocyte size at baseline predicted a decline in insulin sensitivity following a 3.2 kg weight gain over 4 weeks . These recent studies are contrary to the adipose expandability hypothesis and indicate that an increased population of small adipocytes (suggesting hyperplasia) is associated with impaired metabolic health outcomes.
Depot differences in adipose expansion
The opposing associations of upper-body vs lower-body fat distribution with metabolic health are probably due to intrinsic characteristics of WAT depots. Few studies have assessed regional differences in adipogenesis in humans. Depot differences in pre-adipocytes cultured from WAT have been reported, with scABD fat having higher proliferative and differentiation capacity than scFEM fat [19, 20] and VAT . Another adipocyte size assessment suggested depot-specific fat expansion in response to overfeeding: mainly hypertrophy in scABD fat and primarily hyperplasia in scFEM fat .
Sex differences in adipose expansion
Studies in the 1980s reported hyperplastic expansion (higher adipocyte number) of lower-body depots in women and abdominal depots in men . More recent analyses of fat cell size suggest that lower-body adipose tissue expansion is primarily governed by hyperplasia in women but by hypertrophy in men . A higher percentage of early differentiated adipocytes has been identified in the scFEM depot of women relative to men .
In addition to adipose expansion, adipocyte death is a vital component of adipose turnover . Rodent studies reveal an oscillatory pattern of adipose cellularity, including cycles of hypertrophy, hyperplasia and adipocyte death, with increased adipocyte death in obese rodents [25, 26]. Data in humans are scarce. Increased adipocyte death has been implicated in human obesity . Increased response to apoptotic stimuli of VAT (vs scABD fat) pre-adipocytes has been reported [27, 28]. One study suggests that scABD pre-adipocytes from obese women are more susceptible to apoptosis than the scFEM pre-adipocytes . To date, no studies have assessed in vivo adipocyte death in humans and its functional link to fat distribution and metabolic health.
In vivo studies to measure adipose turnover
As highlighted above, established in vitro methods have been employed to assess adipose cellularity and turnover and have yielded valuable information. Primary cultures, as well as functional assays and expression analyses of genes and proteins, have been commonly used to investigate mechanisms of adipogenesis . A standard approach to estimate adipocyte cellularity and lipid content is to determine fat cell size via microscopy or osmium tetroxide fixation . Other assessments in rodents have estimated adipocyte size distributions via microbiopsies of WAT collected at different time points to assess adipocyte cellularity with weight gain . Although in vitro and indirect approaches provide insight into the mechanisms of adipose expansion and adipocyte death, these methods do not provide an assessment in the WAT’s natural milieu. Hence, in vivo approaches are necessary to assess adipose turnover accurately. Nevertheless, the assessment of fat kinetics in vivo has been very difficult in humans, due in part to the slow turnover rate of WAT and the complexity of directly labelling pathway precursors. Although informative in rodents, the incorporation of labelled nucleotides, such as 3H-labelled thymidine or 5-bromodeoxyuridine, involves several limitations, including toxicity and biochemical complications, and thus is not applicable for use in humans. Therefore, despite the broad acceptance of the adipose expandability hypothesis, there is a scarcity of data to describe the in vivo dynamics of adipose turnover and the link with metabolic health in humans. Early studies proposed that adipocytes are produced only during childhood and adolescence  but in vivo evidence is necessary to substantiate adipocyte generation in adulthood. Below, we review two novel and distinct in vivo approaches that have been implemented in humans.
2H labelling method
Hellerstein and colleagues applied the 2H-labelling approach to provide in vivo evidence that adipocytes are generated in humans during adulthood . We have recently assessed in vivo kinetics in subcutaneous WAT from the scABD and scFEM depots using an 8 week incorporation of 2H into adipose cells in obese women . We reported, for the first time, depot differences in in vivo kinetics, with higher adipose cell formation (pre-adipocytes and adipocytes) and TG synthesis rates in the scFEM depot relative to the scABD depot [34, 38]. These data demonstrate that in vivo adipose cell kinetics differ among WAT depots in humans and strengthen other experimental observations that implicate the thigh as a more efficient depot to expand and accommodate lipids in women [2, 5]. Interestingly, adipose cell formation rates in both scABD and scFEM depots were positively correlated with percentage body fat, BMI and visceral adiposity, while negatively associated with insulin sensitivity . These novel data challenge the adipose tissue expandability hypothesis and provide the first evidence of an association between facets of impaired metabolic health and higher, not lower, in vivo adipose cell formation.
Hellerstein’s laboratory was also the first to apply the 2H labelling method to directly measure TG synthesis and turnover in human WAT in vivo . TG half-life was determined to be ~6 months , similar to previous estimates made by indirect techniques . Other laboratories have applied the 2H labelling approach to demonstrate that TG kinetics in WAT plays a significant role in metabolism, reporting that in vivo rates of TG synthesis were significantly lower in insulin-resistant individuals than in insulin-sensitive individuals . Interestingly, we recently identified race and depot differences in TG replacement, with a higher rate of TG synthesis in white vs black individuals and in the scFEM vs scABD depot . These data are intriguing, as race differences in cardiometabolic health have been described .
14C dating method
In vivo adipocyte turnover in humans has also been estimated by measuring the integration of atmospheric 14C, released from nuclear bomb tests during the Cold War (1955–1963), into the genomic DNA of WAT . After cessation of the nuclear bomb testing period, the levels of 14C in the environment exponentially decreased, and 14C was incorporated into plants. The consumption of plants, or animals having eaten plants, resulted in 14C concentrations in the human body reflecting those in the atmosphere at a given time. Hence, this retrospective analysis estimated net changes in adipose turnover over a period of approximately four decades by measuring 14C levels in DNA via accelerator mass spectrometry and relating these values to 14C atmospheric data.
Spalding et al reported that ~8.4% of scABD adipocytes in vivo are replaced every year, regardless of age or degree of obesity . The authors also suggested that adipocyte generation and death rates were in equilibrium in individuals with early onset obesity and that total fat cell number is tightly regulated, even with weight gain or loss. These data suggest that total adipocyte number may be set during childhood and adolescence and constant during adulthood. However, additional studies are necessary to assess fat turnover in individuals with onset of obesity later in life who gradually gain weight over a prolonged period of time, as changes in total adipocyte number may occur. Indeed, one study has shown that total adipocyte number increased in the scFEM depot of women during overfeeding . As in vitro data based on the adipocyte morphology index supports the adipose tissue expandability hypothesis (discussed above), Arner et al observed the relationship of the morphology values to the in vivo generation of adipocytes . Interestingly, individuals displaying more hypertrophic fat expansion (higher morphology index) produced fewer adipocytes in vivo per year than individuals displaying hyperplasia.
Spalding and colleagues also applied the 14C dating method to study long-term in vivo WAT lipid turnover. The mean age of scABD adipocyte TGs, reflected as the duration of TG storage in WAT until irreversible removal via lipolysis (i.e. TG lifespan), was reported to be ~1.6 years . Because the authors estimated adipocyte age as ~9.5 years, this implies that TGs are replaced roughly six times during the adipocyte lifespan. Lower TG age was significantly associated with higher in vitro adipocyte lipolysis (stimulated), implicating lipolysis as an important determinant of TG removal. Interestingly, there was no difference in TG age between sexes or among adipocyte sizes. Net TG storage was calculated to represent the amount of TG stored in WAT each year. Obese individuals had higher TG storage and TG age relative to non-obese individuals, implying that high storage and low removal of adipose TGs may be determinants of obesity . Interestingly, mean TG age, but not TG storage, was correlated with insulin resistance, as assessed by HOMA-IR. Overall, Spalding and colleagues propose that the storage and removal of lipids (TGs), similar to adipocyte turnover, is constant during adulthood. Nevertheless, the lack of variation in TG age as assessed long term does not discount the presence of short-term changes in the dynamics of lipid turnover.
Perspectives on in vivo approaches to measure adipose turnover
Summary of findings from the 2H and 14C in vivo methods
Short term (~8 weeks)
Retrospective (~40 years)
Male and female
Male and female
Lean and obese
scABD and scFEM
↑ in scFEM vs scABD 
Estimated to be equal to adipocyte deaths (~8.4%/year) 
~8.4% adipocyte death/year 
Associations between adipocyte formation vs metabolic health
+ % Body fat and BMI
+ Visceral adiposity
− Insulin sensitivity
↑ TG synthesis in scFEM vs scABD depots 
↑ TG storage in scABD depot of obese vs lean 
↑ TG synthesis in white vs African-American individuals 
↓ TG synthesis in insulin-resistant vs insulin-sensitive individuals 
TG half-life → ~6–12 months 
TG age (i.e. lifespan) → ~1.6 years 
Given the strong association between adipose tissue expandability and turnover with metabolic health, further investigations are necessary to enhance our understanding of the dynamics of adipose kinetics in humans. Our recent data provide in vivo evidence that is contrary to the adipose expandability hypothesis ; however, it is important to note that these analyses provide cross-sectional data and do not reflect causality. To date, there have been no experimental overfeeding studies to truly examine periods of fat expansion in vivo, as individuals with various capacities for adipose expandability may respond differently. Hence, it remains to be seen how extended periods of weight gain and frequent weight cycling in adulthood affect changes in total adipocyte number and turnover and influence energy metabolism. Interestingly, a recently published study by Arner et al  demonstrated that lipolysis is an important predictor of future weight gain and impaired glucose metabolism. Hence, similar prospective studies using an in vivo approach (i.e. 2H labelling) are necessary to clarify the role of adipose turnover in the pathogenesis of insulin resistance and type 2 diabetes. Such in vivo assessments of WAT will yield new knowledge of the dynamics of adipose growth during metabolic diseases, and are likely to direct the discovery of novel therapeutic targets centred on adipocyte generation and death in humans.
Both authors were responsible for drafting the article and revising it critically for important intellectual content. Both authors approved the version to be published.
Work in the authors’ laboratory is partially supported by R01DK090607 (ER) and by a Nutrition Obesity Research Center (NORC) Grant P30DK072476 (ER) through the National Institutes of Health. Work in the authors’ laboratory is also supported by K01DK100527 (UW) and R03DK112006 (UW) from the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health, which are funding sources for UW.
Duality of interest
The authors declare that there is no duality of interest associated with this manuscript.
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