Limits...
Glycerol Production from Glucose and Fructose by 3T3-L1 Cells: A Mechanism of Adipocyte Defense from Excess Substrate.

Romero Mdel M, Sabater D, Fernández-López JA, Remesar X, Alemany M - PLoS ONE (2015)

Bottom Line: Fructose conversion to lactate and glycerol was lower than that of glucose.When both hexoses were present, the effects of fructose on gene expression prevailed over those of glucose.A phosphatase pathway such as that described may have a potential regulatory function, and explain the production of glycerol by adipocytes in the absence of lipolytic stimulation.

View Article: PubMed Central - PubMed

Affiliation: Department of Nutrition and Food Science, Faculty of Biology, University of Barcelona, Av.Diagonal 643, 08028, Barcelona, Spain; Institute of Biomedicine, University of Barcelona, Barcelona, Spain; CIBER Obesity and Nutrition, Barcelona, Spain.

ABSTRACT
Cultured adipocytes (3T3-L1) produce large amounts of 3C fragments; largely lactate, depending on medium glucose levels. Increased glycolysis has been observed also in vivo in different sites of rat white adipose tissue. We investigated whether fructose can substitute glucose as source of lactate, and, especially whether the glycerol released to the medium was of lipolytic or glycolytic origin. Fructose conversion to lactate and glycerol was lower than that of glucose. The fast exhaustion of medium glucose was unrelated to significant changes in lipid storage. Fructose inhibited to a higher degree than glucose the expression of lipogenic enzymes. When both hexoses were present, the effects of fructose on gene expression prevailed over those of glucose. Adipocytes expressed fructokinase, but not aldolase b. Substantive release of glycerol accompanied lactate when fructose was the substrate. The mass of cell triacylglycerol (and its lack of change) could not justify the comparatively higher amount of glycerol released. Consequently, most of this glycerol should be derived from the glycolytic pathway, since its lipolytic origin could not be (quantitatively) sustained. Proportionally (with respect to lactate plus glycerol), more glycerol was produced from fructose than from glucose, which suggests that part of fructose was catabolized by the alternate (hepatic) fructose pathway. Earlier described adipose glycerophophatase activity may help explain the glycolytic origin of most of the glycerol. However, no gene is known for this enzyme in mammals, which suggests that this function may be carried out by one of the known phosphatases in the tissue. Break up of glycerol-3P to yield glycerol, may be a limiting factor for the synthesis of triacylglycerols through control of glycerol-3P availability. A phosphatase pathway such as that described may have a potential regulatory function, and explain the production of glycerol by adipocytes in the absence of lipolytic stimulation.

No MeSH data available.


Related in: MedlinePlus

Microphotographs of 3T3-L1 cells in culture.The cells shown were maintained under the conditions described in the text. They are representative of the conditions used throughout the whole study. Photographs A and B are shown at a lower magnifying power than C and D. A white bar shows a reference for size. Panes A and C correspond to an ordinary 3T3-L1 culture, in which differentiated adipocytes and undifferentiated fibroblasts coexist. Panels B and D represent 3T3-L1 cultures incubates using Transwells, as described for this study. All wells used in this investigation were maintained under these same conditions; there was a total absence of undifferentiated fibroblasts, as previously described [17]
© Copyright Policy
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC4591265&req=5

pone.0139502.g001: Microphotographs of 3T3-L1 cells in culture.The cells shown were maintained under the conditions described in the text. They are representative of the conditions used throughout the whole study. Photographs A and B are shown at a lower magnifying power than C and D. A white bar shows a reference for size. Panes A and C correspond to an ordinary 3T3-L1 culture, in which differentiated adipocytes and undifferentiated fibroblasts coexist. Panels B and D represent 3T3-L1 cultures incubates using Transwells, as described for this study. All wells used in this investigation were maintained under these same conditions; there was a total absence of undifferentiated fibroblasts, as previously described [17]

Mentions: Fig 1 depicts an example of standard 3T3-L1 cells two days after the beginning of the incubation in the presence of 11 mM glucose, compared with a standard 3T3-L1 cell culture incubated with the same medium but not using Transwells [17]. There was a marked absence of fibroblasts under the conditions of incubation used, in comparison with their common presence in the standard culture,


Glycerol Production from Glucose and Fructose by 3T3-L1 Cells: A Mechanism of Adipocyte Defense from Excess Substrate.

Romero Mdel M, Sabater D, Fernández-López JA, Remesar X, Alemany M - PLoS ONE (2015)

Microphotographs of 3T3-L1 cells in culture.The cells shown were maintained under the conditions described in the text. They are representative of the conditions used throughout the whole study. Photographs A and B are shown at a lower magnifying power than C and D. A white bar shows a reference for size. Panes A and C correspond to an ordinary 3T3-L1 culture, in which differentiated adipocytes and undifferentiated fibroblasts coexist. Panels B and D represent 3T3-L1 cultures incubates using Transwells, as described for this study. All wells used in this investigation were maintained under these same conditions; there was a total absence of undifferentiated fibroblasts, as previously described [17]
© Copyright Policy
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4591265&req=5

pone.0139502.g001: Microphotographs of 3T3-L1 cells in culture.The cells shown were maintained under the conditions described in the text. They are representative of the conditions used throughout the whole study. Photographs A and B are shown at a lower magnifying power than C and D. A white bar shows a reference for size. Panes A and C correspond to an ordinary 3T3-L1 culture, in which differentiated adipocytes and undifferentiated fibroblasts coexist. Panels B and D represent 3T3-L1 cultures incubates using Transwells, as described for this study. All wells used in this investigation were maintained under these same conditions; there was a total absence of undifferentiated fibroblasts, as previously described [17]
Mentions: Fig 1 depicts an example of standard 3T3-L1 cells two days after the beginning of the incubation in the presence of 11 mM glucose, compared with a standard 3T3-L1 cell culture incubated with the same medium but not using Transwells [17]. There was a marked absence of fibroblasts under the conditions of incubation used, in comparison with their common presence in the standard culture,

Bottom Line: Fructose conversion to lactate and glycerol was lower than that of glucose.When both hexoses were present, the effects of fructose on gene expression prevailed over those of glucose.A phosphatase pathway such as that described may have a potential regulatory function, and explain the production of glycerol by adipocytes in the absence of lipolytic stimulation.

View Article: PubMed Central - PubMed

Affiliation: Department of Nutrition and Food Science, Faculty of Biology, University of Barcelona, Av.Diagonal 643, 08028, Barcelona, Spain; Institute of Biomedicine, University of Barcelona, Barcelona, Spain; CIBER Obesity and Nutrition, Barcelona, Spain.

ABSTRACT
Cultured adipocytes (3T3-L1) produce large amounts of 3C fragments; largely lactate, depending on medium glucose levels. Increased glycolysis has been observed also in vivo in different sites of rat white adipose tissue. We investigated whether fructose can substitute glucose as source of lactate, and, especially whether the glycerol released to the medium was of lipolytic or glycolytic origin. Fructose conversion to lactate and glycerol was lower than that of glucose. The fast exhaustion of medium glucose was unrelated to significant changes in lipid storage. Fructose inhibited to a higher degree than glucose the expression of lipogenic enzymes. When both hexoses were present, the effects of fructose on gene expression prevailed over those of glucose. Adipocytes expressed fructokinase, but not aldolase b. Substantive release of glycerol accompanied lactate when fructose was the substrate. The mass of cell triacylglycerol (and its lack of change) could not justify the comparatively higher amount of glycerol released. Consequently, most of this glycerol should be derived from the glycolytic pathway, since its lipolytic origin could not be (quantitatively) sustained. Proportionally (with respect to lactate plus glycerol), more glycerol was produced from fructose than from glucose, which suggests that part of fructose was catabolized by the alternate (hepatic) fructose pathway. Earlier described adipose glycerophophatase activity may help explain the glycolytic origin of most of the glycerol. However, no gene is known for this enzyme in mammals, which suggests that this function may be carried out by one of the known phosphatases in the tissue. Break up of glycerol-3P to yield glycerol, may be a limiting factor for the synthesis of triacylglycerols through control of glycerol-3P availability. A phosphatase pathway such as that described may have a potential regulatory function, and explain the production of glycerol by adipocytes in the absence of lipolytic stimulation.

No MeSH data available.


Related in: MedlinePlus