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1 Departments of Medicine, 2 Pathology, and 3 Biochemistry, Boston University, Boston, Massachusetts 02118
Fat mass, adipocyte size and metabolic
responsiveness, and preadipocyte differentiation decrease between
middle and old age. We show that expression of CCAAT/enhancer binding
protein (C/EBP)-
, a key regulator of adipogenesis and fat cell
function, declined substantially with aging in differentiating
preadipocytes cultured under identical conditions from rats of various
ages. Overexpression of C/EBP
in preadipocytes cultured from old
rats restored capacity to differentiate into fat cells, indicating that
downstream differentiation-dependent genes maintain responsiveness to
regulators of adipogenesis. C/EBP
-expression also decreased with age
in fat tissue from three different depots and in isolated fat cells.
The overall level of C/EBP
, which modulates
C/EBP
-expression, did not change with age, but the truncated,
dominant-negative C/EBP
-liver inhibitory protein (LIP) isoform
increased in cultured preadipocytes and isolated fat cells. Overexpression of C/EBP
-LIP in preadipocytes from young rats impaired adipogenesis. C/EBP
, which acts with full-length C/EBP
to enhance adipogenesis, decreased with age. Thus processes intrinsic to adipose cells involving changes in C/EBP family members contribute to impaired adipogenesis and altered fat tissue function with aging.
These effects are potentially reversible.
preadipocytes; differentiation; C/EBP
; C/EBP
; c/EBP
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