Induction of Adipocyte Differentiation by a Thiazolidinedione in Cultured, Subepidermal, Fibroblast-Like Cells of an Infant with Congenital Generalized Lipodystrophy
Author(s) -
Pamela FischerPosovszky,
Peter Möller,
L. Bindl,
Ingo Melzner,
Hans Törnqvist,
KlausMichael Debatin,
Martin Wabitsch
Publication year - 2002
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jcem.87.5.8467
Subject(s) - endocrinology , medicine , adipose tissue , lipodystrophy , adipocyte , adipogenesis , fibroblast , leptin , thiazolidinedione , rosiglitazone , foreskin , biology , cellular differentiation , adipose tissue macrophages , 3t3 l1 , cell culture , microbiology and biotechnology , insulin , white adipose tissue , immunology , diabetes mellitus , biochemistry , genetics , human immunodeficiency virus (hiv) , viral load , antiretroviral therapy , type 2 diabetes , gene , obesity
Congenital generalized lipodystrophy (CGL) is characterized by the absence of adipose tissue from birth due to a hypothetical differentiation block. The genetic causes of CGL are still not completely understood. Subepidermal, fibroblast-like cells were prepared from the sc tissue of an infant with CGL. Preadipocytes from sc adipose tissue and foreskin fibroblasts from three healthy patients, respectively, were used as controls. Adipose differentiation was induced in cultured cells by exposure to 10 nM insulin, 200 pM T(3), 1 microM cortisol, and 2 microM rosiglitazone. Under these conditions 42% of the subepidermal, fibroblast-like CGL cells developed into mature adipocytes. Adipogenic differentiation was dependent on rosiglitazone. The differentiation rate was comparable in cultures of preadipocytes from control patients maintained under the same conditions (53%, 38%, and 20%). In contrast, foreskin fibroblasts did not differentiate into adipocytes. Morphological changes in CGL cells during differentiation were associated with the expression of fat cell-specific mRNAs (PPARgamma, leptin, and glut-4). In addition, these cells revealed characteristic features of mature adipocytes, such as lipogenesis or leptin secretion. Taken together, we show that adipocyte precursor cells were present in subepidermal tissue of a patient with CGL and were able to differentiate into adipocytes in the presence of a thiazolidinedione. These findings strongly support clinical trials with thiazolidinediones in patients with CGL.
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