Hepatic CEACAM1 over-expression protects against diet-induced fibrosis and inflammation in white adipose tissue

Sumona G. Lester, Lucia Russo, Simona Ghanem, Saja S. Khuder, Anthony M. DeAngelis, Emily L. Esakov, Thomas A. Bowman, Garrett Heinrich, Qusai Y. Al-Share, Marcia F. McInerney, William M. Philbrick, Sonia M. Najjar

Research output: Contribution to journalArticle

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Abstract

CEACAM1 promotes insulin extraction, an event that occurs mainly in liver. Phenocopying global Ceacam1 null mice (Cc1–/–), C57/BL6J mice fed a high-fat (HF) diet exhibited reduced hepatic CEACAM1 levels and impaired insulin clearance, followed by hyperinsulinemia, insulin resistance, and visceral obesity. Conversely, forced liver-specific expression of CEACAM1 protected insulin sensitivity and energy expenditure, and limited gain in total fat mass by HF diet in L-CC1 mice. Because CEACAM1 protein is barely detectable in white adipose tissue (WAT), we herein investigated whether hepatic CEACAM1-dependent insulin clearance pathways regulate adipose tissue biology in response to dietary fat. While HF diet caused a similar body weight gain in L-CC1, this effect was delayed and less intense relative to wild-type (WT) mice. Histological examination revealed less expansion of adipocytes in L-CC1 than WT by HF intake. Immunofluorescence analysis demonstrated a more limited recruitment of crown-like structures, and qRT-PCR analysis showed no significant rise in TNFα mRNA levels in response to HF intake in L-CC1 than WT mice. Unlike WT, HF diet did not activate TGF-β in WAT of L-CC1 mice, as assessed by Western analysis of Smad2/3 phosphorylation. Consistently, HF diet caused relatively less collagen deposition in L-CC1 than WT mice, as shown by Trichrome staining. Coupled with reduced lipid redistribution from liver to visceral fat, lower inflammation and fibrosis could contribute to protected energy expenditure against HF diet in L-CC1 mice. The data underscore the important role of hepatic insulin clearance in the regulation of adipose tissue inflammation and fibrosis.

Original languageEnglish
Article numberY
JournalFrontiers in Endocrinology
Volume6
DOIs
Publication statusPublished - 1 Jan 2015

Fingerprint

White Adipose Tissue
High Fat Diet
Fibrosis
Diet
Inflammation
Liver
Insulin
Fats
Energy Metabolism
Insulin Resistance
Adipose Tissue
Intra-Abdominal Fat
Abdominal Obesity
CD66 antigens
Dietary Fats
Hyperinsulinism
Crowns
Adipocytes
Weight Gain
Fluorescent Antibody Technique

Keywords

  • CEACAM1
  • Fibrosis
  • Inflammation
  • Insulin clearance
  • Insulin resistance
  • Liver-adipose tissue axis
  • Steatosis

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism

Cite this

Hepatic CEACAM1 over-expression protects against diet-induced fibrosis and inflammation in white adipose tissue. / Lester, Sumona G.; Russo, Lucia; Ghanem, Simona; Khuder, Saja S.; DeAngelis, Anthony M.; Esakov, Emily L.; Bowman, Thomas A.; Heinrich, Garrett; Al-Share, Qusai Y.; McInerney, Marcia F.; Philbrick, William M.; Najjar, Sonia M.

In: Frontiers in Endocrinology, Vol. 6, Y, 01.01.2015.

Research output: Contribution to journalArticle

Lester, SG, Russo, L, Ghanem, S, Khuder, SS, DeAngelis, AM, Esakov, EL, Bowman, TA, Heinrich, G, Al-Share, QY, McInerney, MF, Philbrick, WM & Najjar, SM 2015, 'Hepatic CEACAM1 over-expression protects against diet-induced fibrosis and inflammation in white adipose tissue', Frontiers in Endocrinology, vol. 6, Y. https://doi.org/10.3389/fendo.2015.00116
Lester, Sumona G. ; Russo, Lucia ; Ghanem, Simona ; Khuder, Saja S. ; DeAngelis, Anthony M. ; Esakov, Emily L. ; Bowman, Thomas A. ; Heinrich, Garrett ; Al-Share, Qusai Y. ; McInerney, Marcia F. ; Philbrick, William M. ; Najjar, Sonia M. / Hepatic CEACAM1 over-expression protects against diet-induced fibrosis and inflammation in white adipose tissue. In: Frontiers in Endocrinology. 2015 ; Vol. 6.
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AU - DeAngelis, Anthony M.

AU - Esakov, Emily L.

AU - Bowman, Thomas A.

AU - Heinrich, Garrett

AU - Al-Share, Qusai Y.

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