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SPARC-null mice exhibit increased adiposity without significant differences in overall body weight
A D Bradshaw1, D C Graves, K Motamed
1Department of Vascular Biology, Hope Heart Institute, Seattle, WA 98104, USA.
Abstract:
Secreted protein acidic and rich in cysteine/osteonectin/BM-40 (SPARC) is a matrix-associated protein that elicits changes in cell shape, inhibits cell-cycle progression, and influences the synthesis of extracellular matrix (ECM). The absence of SPARC in mice gives rise to aberrations in the structure and composition of the ECM that result in generation of cataracts, development of severe osteopenia, and accelerated closure of dermal wounds. In this report we show that SPARC-null mice have greater deposits of s.c. fat and larger epididymal fat pads in comparison with wild-type mice. Similar to earlier studies of SPARC-null dermis, we observed a reduction in collagen I in SPARC-null fat pads in comparison with wild-type. Although elevated levels of serum leptin were observed in SPARC-null mice, their overall body weights were not significantly different from those of wild-type counterparts. The diameters of adipocytes from SPARC-null versus wild-type epididymal fat pads were 252 +/- 61 and 161 +/- 33 microm (means +/- SD), respectively, and there was an increase in adipocyte number within SPARC-null fat pads in comparison with wild-type pads. Thus the absence of SPARC appears to result in an increase in the size of individual adipocytes as well as an increase in the number of adipocytes per fat pad. In fat pads isolated from wild-type mice, SPARC mRNA was associated with both the stromal/vascular and adipocyte fractions. We propose that SPARC limits the accumulation of adipose tissue in mice in part through its demonstrated effects on the regulation of cell shape and production of ECM.
Insights
Secreted protein acidic and rich in cysteine (SPARC) deficiency in mice leads to increased adipose tissue accumulation. SPARC absence results in larger adipocytes and more numerous fat cells, suggesting SPARC limits fat tissue growth.
Area of Science:
- Biochemistry
- Cell Biology
- Physiology
Background:
- Secreted protein acidic and rich in cysteine (SPARC) is an extracellular matrix (ECM) protein influencing cell behavior and ECM synthesis.
- SPARC deficiency in mice causes ECM abnormalities, cataracts, osteopenia, and rapid wound healing.
- SPARC-null mice exhibit altered adipose tissue characteristics.
Purpose of the Study:
- To investigate the role of SPARC in adipose tissue regulation.
- To determine the impact of SPARC absence on adipocyte size, number, and ECM composition.
- To explore the potential mechanisms by which SPARC affects fat accumulation.
Main Methods:
- Comparison of adipose tissue from SPARC-null and wild-type mice.
- Analysis of adipocyte size and number in epididymal fat pads.
- Assessment of collagen I levels in adipose tissue.
- Quantification of SPARC mRNA in stromal/vascular and adipocyte fractions.
Main Results:
- SPARC-null mice showed increased subcutaneous fat deposits and larger epididymal fat pads.
- Reduced collagen I content was observed in SPARC-null fat pads.
- SPARC-null mice had significantly larger adipocyte diameters and increased adipocyte numbers.
- Elevated serum leptin levels were noted in SPARC-null mice without significant body weight differences.
Conclusions:
- SPARC absence leads to increased adipose tissue mass due to enhanced adipocyte size and number.
- SPARC may limit adipose tissue accumulation by regulating adipocyte shape and ECM production.
- These findings highlight SPARC's role in metabolic regulation and adipose tissue homeostasis.

