## Abstract The role of the inositol lipid 5βphosphatase (SHIP2) in preadipocyte signaling is not known. Although overexpression of SHIP2 inhibited proliferation and ^3^Hβthymidine incorporation in 3T3βL1 preadipocytes, there was no effect on insulinβinduced adipogenesis. Insulin promoted SHIP2 tyr
Interaction of plasma lipoprotein subfractions with differentiating 3T3-L1 and human mammary preadipocytes in culture
β Scribed by Lee-Anne Stanton; Maryna van de Venter; Willem Oelofsen
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 158 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
β¦ Synopsis
Differentiating 3T3-L1 preadipocytes (murine fatty fibroblasts) and human preadipocytes interact with human lipoprotein subfractions (HDL 2 and LDL II/III ) at all stages of the differentiation program, displaying saturable binding behavior. Both cell types interact similarly with LDL II/III as differentiation proceeds, showing increased binding affinities and capacities and maximal rates of uptake in the mature cells, as compared with the preadipocyte stage. These changes coincide with the intracellular appearance of lipid droplets. However, with regard to HDL 2 , a markedly different pattern of interaction is evident in both cell types. For 3T3-L1 cells, lowered binding and uptake affinities and capacities are apparent in the fully differentiated state for HDL 2 , as compared with LDL II/III . Human preadipocytes displayed two distinct affinity binding sites for HDL 2 during the early stages of differentiation (days 2 and 3), as compared with a single affinity site for LDL II/III at all stages. However, in the fully differentiated human cells, only a single affinity site, indistinguishable from the high-affinity site present on day 2, is evident, and probably represents the only binding site of physiological significance in these cells. All the cellular developments appear to be largely unaffected by exposure of both preadipocyte types to added lipoproteins (HDL Ο© LDL) in the medium during the early stages of the conversion process.
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