MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes

We investigated for the first time the expression of melanoma cell adhesion molecule (MCAM) and its involvement in the differentiation of 3T3-L1 fibroblasts to adipocytes. We found that MCAM mRNA increased subsequent to the activation of the master regulator of adipogenesis, PPARγ, and this increase...

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Publicado: 2018
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v448_n1-2_p299_Gabrielli
http://hdl.handle.net/20.500.12110/paper_03008177_v448_n1-2_p299_Gabrielli
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spelling paper:paper_03008177_v448_n1-2_p299_Gabrielli2023-06-08T15:27:29Z MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes 3T3-L1 fibroblasts Adipogenesis C/EBP beta MCAM/CD146 PPAR gamma adiponectin beta catenin CCAAT enhancer binding protein beta CD146 antigen messenger RNA mitogen activated protein kinase perilipin 1 peroxisome proliferator activated receptor gamma CD146 antigen Mcam protein, mouse peroxisome proliferator activated receptor gamma 3T3-L1 cell line adipocyte adipogenesis animal cell Article cell differentiation cell maturation controlled study down regulation enzyme activation gene expression gene knockdown immunofluorescence microscopy mouse mRNA expression level NIH 3T3 cell line nonhuman protein expression level protein function quantitative analysis real time polymerase chain reaction upregulation Western blotting 3T3-L1 cell line adipocyte adipogenesis animal biosynthesis cytology fibroblast gene expression regulation gene knockdown genetics metabolism 3T3-L1 Cells Adipocytes Adipogenesis Animals CD146 Antigen Cell Differentiation Fibroblasts Gene Expression Regulation Gene Knockdown Techniques Mice PPAR gamma We investigated for the first time the expression of melanoma cell adhesion molecule (MCAM) and its involvement in the differentiation of 3T3-L1 fibroblasts to adipocytes. We found that MCAM mRNA increased subsequent to the activation of the master regulator of adipogenesis, PPARγ, and this increase was maintained in the mature adipocytes. On the other hand, MCAM knockdown impaired differentiation and induction of PPARγ as well as expression of genes activated by PPARγ. However, events that precede and are necessary for early PPARγ activation, such as C/EBPβ induction, β-catenin downregulation, and ERK activation, were not affected in the MCAM knockdown cells. In keeping with this, the increase in PPARγ mRNA that precedes MCAM induction was not altered in the knockdown cells. In conclusion, our findings suggest that MCAM is a gene upregulated and involved in maintaining PPARγ induction in the late but not in the early stages of 3T3-L1 fibroblasts adipogenesis. © 2018, Springer Science+Business Media, LLC, part of Springer Nature. 2018 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v448_n1-2_p299_Gabrielli http://hdl.handle.net/20.500.12110/paper_03008177_v448_n1-2_p299_Gabrielli
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 3T3-L1 fibroblasts
Adipogenesis
C/EBP beta
MCAM/CD146
PPAR gamma
adiponectin
beta catenin
CCAAT enhancer binding protein beta
CD146 antigen
messenger RNA
mitogen activated protein kinase
perilipin 1
peroxisome proliferator activated receptor gamma
CD146 antigen
Mcam protein, mouse
peroxisome proliferator activated receptor gamma
3T3-L1 cell line
adipocyte
adipogenesis
animal cell
Article
cell differentiation
cell maturation
controlled study
down regulation
enzyme activation
gene expression
gene knockdown
immunofluorescence microscopy
mouse
mRNA expression level
NIH 3T3 cell line
nonhuman
protein expression level
protein function
quantitative analysis
real time polymerase chain reaction
upregulation
Western blotting
3T3-L1 cell line
adipocyte
adipogenesis
animal
biosynthesis
cytology
fibroblast
gene expression regulation
gene knockdown
genetics
metabolism
3T3-L1 Cells
Adipocytes
Adipogenesis
Animals
CD146 Antigen
Cell Differentiation
Fibroblasts
Gene Expression Regulation
Gene Knockdown Techniques
Mice
PPAR gamma
spellingShingle 3T3-L1 fibroblasts
Adipogenesis
C/EBP beta
MCAM/CD146
PPAR gamma
adiponectin
beta catenin
CCAAT enhancer binding protein beta
CD146 antigen
messenger RNA
mitogen activated protein kinase
perilipin 1
peroxisome proliferator activated receptor gamma
CD146 antigen
Mcam protein, mouse
peroxisome proliferator activated receptor gamma
3T3-L1 cell line
adipocyte
adipogenesis
animal cell
Article
cell differentiation
cell maturation
controlled study
down regulation
enzyme activation
gene expression
gene knockdown
immunofluorescence microscopy
mouse
mRNA expression level
NIH 3T3 cell line
nonhuman
protein expression level
protein function
quantitative analysis
real time polymerase chain reaction
upregulation
Western blotting
3T3-L1 cell line
adipocyte
adipogenesis
animal
biosynthesis
cytology
fibroblast
gene expression regulation
gene knockdown
genetics
metabolism
3T3-L1 Cells
Adipocytes
Adipogenesis
Animals
CD146 Antigen
Cell Differentiation
Fibroblasts
Gene Expression Regulation
Gene Knockdown Techniques
Mice
PPAR gamma
MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
topic_facet 3T3-L1 fibroblasts
Adipogenesis
C/EBP beta
MCAM/CD146
PPAR gamma
adiponectin
beta catenin
CCAAT enhancer binding protein beta
CD146 antigen
messenger RNA
mitogen activated protein kinase
perilipin 1
peroxisome proliferator activated receptor gamma
CD146 antigen
Mcam protein, mouse
peroxisome proliferator activated receptor gamma
3T3-L1 cell line
adipocyte
adipogenesis
animal cell
Article
cell differentiation
cell maturation
controlled study
down regulation
enzyme activation
gene expression
gene knockdown
immunofluorescence microscopy
mouse
mRNA expression level
NIH 3T3 cell line
nonhuman
protein expression level
protein function
quantitative analysis
real time polymerase chain reaction
upregulation
Western blotting
3T3-L1 cell line
adipocyte
adipogenesis
animal
biosynthesis
cytology
fibroblast
gene expression regulation
gene knockdown
genetics
metabolism
3T3-L1 Cells
Adipocytes
Adipogenesis
Animals
CD146 Antigen
Cell Differentiation
Fibroblasts
Gene Expression Regulation
Gene Knockdown Techniques
Mice
PPAR gamma
description We investigated for the first time the expression of melanoma cell adhesion molecule (MCAM) and its involvement in the differentiation of 3T3-L1 fibroblasts to adipocytes. We found that MCAM mRNA increased subsequent to the activation of the master regulator of adipogenesis, PPARγ, and this increase was maintained in the mature adipocytes. On the other hand, MCAM knockdown impaired differentiation and induction of PPARγ as well as expression of genes activated by PPARγ. However, events that precede and are necessary for early PPARγ activation, such as C/EBPβ induction, β-catenin downregulation, and ERK activation, were not affected in the MCAM knockdown cells. In keeping with this, the increase in PPARγ mRNA that precedes MCAM induction was not altered in the knockdown cells. In conclusion, our findings suggest that MCAM is a gene upregulated and involved in maintaining PPARγ induction in the late but not in the early stages of 3T3-L1 fibroblasts adipogenesis. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
title MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
title_short MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
title_full MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
title_fullStr MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
title_full_unstemmed MCAM knockdown impairs PPARγ expression and 3T3-L1 fibroblasts differentiation to adipocytes
title_sort mcam knockdown impairs pparγ expression and 3t3-l1 fibroblasts differentiation to adipocytes
publishDate 2018
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v448_n1-2_p299_Gabrielli
http://hdl.handle.net/20.500.12110/paper_03008177_v448_n1-2_p299_Gabrielli
_version_ 1768541937306959872