Reduced β-cell mass in MCH-KO mice on normal chow and high-fat diets.

Slides:



Advertisements
Similar presentations
Figure 1 Body weight of control and BPA-treated mothers after delivery
Advertisements

Arterioscler Thromb Vasc Biol
The gene encoding TP53INP1 is expressed in pancreatic endocrine cells A, B(A, B) Immunocytofluorescent staining of TP53INP1 (red) and insulin (green) in.
Insulin and glucagon secretion: nondiabetic and diabetic subjects.
Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell
Expression of IL-1α in goblet cells and their destruction during DSS-induced colitis. Expression of IL-1α in goblet cells and their destruction during.
Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell
Corrigendum to “Lipocalin-2 mediates non-alcoholic steatohepatitis by promoting neutrophil-macrophage crosstalk via the induction of CXCR2”  Dewei Ye,
by Ling-juan Zhang, Christian F. Guerrero-Juarez, Tissa Hata, Sagar P
Volume 142, Issue 7, Pages e6 (June 2012)
Volume 1, Issue 2, Pages (February 2005)
TrkB-T1 is upregulated in cerebellum of Pex14ΔC/ΔC BL/ICR mouse at P3.
Volume 14, Issue 5, Pages (November 2011)
Volume 1, Issue 4, Pages (April 2005)
BDNF expression in the cerebellum and brain stem region.
Quantitative RT-PCR results of relative gene expression normalized to wild-type (WT) expression levels for the LjMYB14 transgene (A) and genes specific.
Identification of SH2-B as a key regulator of leptin sensitivity, energy balance, and body weight in mice  Decheng Ren, Minghua Li, Chaojun Duan, Liangyou.
Diabetic FXR KO kidney showed increased lipid accumulation.
INT-747 treatment showed antifibrotic, anti-inflammatory, and antioxidative effects on diabetic DBA/2J mice. INT-747 treatment showed antifibrotic, anti-inflammatory,
Decreased P-IR and total FOXO1 levels in an HFS diet.
Cellularity of epididymal adipose tissue.
Exogenous CRP administration causes fasting hyperglycemia and hyperinsulinemia without altering body composition. Exogenous CRP administration causes fasting.
SIRT1 is downregulated in human gastric cancer (GC).
Volume 4, Issue 5, Pages (November 2006)
α-Cells mainly express SSTR2 and SSTR3
Nrf2−/− mice had higher TGF-β1 transcription and FN expression.
Human and mouse islets express MCH and MCHR1.
GLUT4 LXRE is required for downregulation of adipose GLUT4 mRNA during fasting and diet-induced obesity. GLUT4 LXRE is required for downregulation of adipose.
Skeletal muscle characteristics of HFD-induced obese mice.
Fragment N expression does not affect islet morphology and cellularity
Smad3-KO adipose tissues have increased FA uptake and β-oxidation.
Zn2+ and NAD(P)H content in Mafa∆panc and Mafa∆panc;Mafb+/− β-cells.
Loss of protection by linagliptin against obesity-related inflammation and insulin resistance in MIP-1α−/− mice. Loss of protection by linagliptin against.
Transgenic restoration of long-chain n-3 PUFA protects against obesity-linked insulin resistance and glucose intolerance. Transgenic restoration of long-chain.
A–E: Mechanisms underlying the blunted adiponectin secretion in adipocytes from obese/type 2 diabetic mice. A–E: Mechanisms underlying the blunted adiponectin.
Effect of berberine on white adipose tissue mass.
Grg3 is expressed in most β-cells but less frequently in α-cells.
MiRNA expression profiling in adipocytes from wild-type (WT) and leptin-deficient ob/ob mice. miRNA expression profiling in adipocytes from wild-type (WT)
GLP-1 and gastrin combination therapy increases pancreatic insulin content (A) and β-cell mass (B) in NOD mice. GLP-1 and gastrin combination therapy increases.
Reduced OXPHOS expression and increased UCP expression.
Western blot analysis of α-Syn-BAC-Tg/GBA-hetero-KO mice at multiple time points. Western blot analysis of α-Syn-BAC-Tg/GBA-hetero-KO mice at multiple.
AgRP-ATF4 KO mice have decreased food intake and enhanced energy expenditure. AgRP-ATF4 KO mice have decreased food intake and enhanced energy expenditure.
Metabolic parameters of Id1−/− and wild-type mice fed a standard chow diet (hatched bars and striped bars, respectively) or a high-fat diet (black bars.
SENP2 overexpression increases FAO by upregulating expression of FAO-associated enzymes in muscle. SENP2 overexpression increases FAO by upregulating expression.
Effect of Id1 deletion on insulin action in wild-type and Id1−/− mice fed a chow diet (white triangle/striped bar and black triangle/hatched bar, respectively)
MϕRIP140KD mice show browning in vWAT.
Liver fibrosis after CCl4 injury in 5αR1-KO and WT mice.
Hepatic fuel metabolism in male 5αR1-KO and WT mice
Insulin resistance and hepatic steatosis in ASKO mice.
Treatment of high-fat diet–fed mice with TTR-ASOs decreases circulating TTR and RBP4 levels, and improves insulin sensitivity. Treatment of high-fat diet–fed.
PEDF inhibits Wnt/T-cell factor/β-catenin signaling in resting and wounded skin. PEDF inhibits Wnt/T-cell factor/β-catenin signaling in resting and wounded.
Effects of chow-diet feeding on control and TRIB3 MOE mice.
MANF expression is required for maintaining β-cell mass.
Glucose-stimulated insulin secretion, plasma glucagon levels, and pancreatic hormone contents. Glucose-stimulated insulin secretion, plasma glucagon levels,
High-fat diet–induced glucose intolerance is prevented in ghrelin knockout (Ghr-KO) mice. High-fat diet–induced glucose intolerance is prevented in ghrelin.
A: Gene expression of β-myosin heavy chain (hypertrophic marker) was analyzed on real-time PCR and normalized against 18S expression. n = 8–11 for each.
The activity of transcription factor CREBP downstream of MEK signaling is markedly reduced in insulin-resistant macrophages. The activity of transcription.
Chronic rapamycin treatment impairs β-cell mass and insulin clearance in rats. Chronic rapamycin treatment impairs β-cell mass and insulin clearance in.
A–G: Reduced β3AR and Epac1 protein in HFD adipocytes as well as blunted epinephrine-stimulated adiponectin secretion upon β3AR and Epac1 siRNA knockdown.
Mice lacking Y1 receptor in the hematopoietic compartment remain healthy under normal chow feeding conditions. Mice lacking Y1 receptor in the hematopoietic.
IKKβ protects adipocytes from HFD-induced cell death.
Decreased M1 and increased M2 macrophages in eWAT and liver of DIO mice due to linagliptin administration. Decreased M1 and increased M2 macrophages in.
IL-17A mediates cutaneous GVHD
Aggregation and toxicity of α-synuclein in HEK293T cells.
EMT gene expression patterns of M-Wnt and E-Wnt cells in vitro and in vivo. EMT gene expression patterns of M-Wnt and E-Wnt cells in vitro and in vivo.
Osteoactivin expression is required for the invasive phenotype of in vivo selected bone metastatic 4T1 breast cancer cells. Osteoactivin expression is.
Expression of PCNA, K10, and K5 in skin lesions from Stat3+/−:HPV8 and Stat3+/+:HPV8 mice. Expression of PCNA, K10, and K5 in skin lesions from Stat3+/−:HPV8.
Reduced β-catenin and cyclin D1 expression and increased apoptosis in lactating mammary gland epithelia of DDTg mice. Reduced β-catenin and cyclin D1 expression.
NRP2 expression is associated with prostate cancer progression.
Fig. 1 Obesity-related adipocyte degeneration and cfDNA release.
Presentation transcript:

Reduced β-cell mass in MCH-KO mice on normal chow and high-fat diets. Reduced β-cell mass in MCH-KO mice on normal chow and high-fat diets. Representative pancreas sections (A) and quantitation of β-cell mass (B) from control and MCH-KO mice backcrossed on the 129Sv or C57Bl/6 genetic backgrounds. *P < 0.05, wild type vs. KO, n = 4. Sections are immunostained with a cocktail of antibodies against non–β-cell hormones (dark brown) and counterstained with hematoxylin (blue) as described in research design and methods. Representative pancreas sections (C) and quantitation of β-cell mass (D) of control and MCH-KO mice fed normal chow (left panel) or a high-fat (right panel) diet, immunostained with a cocktail of antibodies against non–β-cell hormones (dark brown) and counterstained with hematoxylin (blue). *P < 0.05 wild-type chow vs. wild-type high-fat fed, n = 4; †P < 0.05, wild-type chow vs. KO chow fed, n = 4. Alterations in expression of MCH (E) or MCHR1 (F) in wild-type mice on a chow or high-fat diet determined using real-time PCR. For E, P < 0.01, n = 4; for F, P = 0.07, n = 4. Alterations in α-cell mass in wild-type or MCH-KO mice on the B6 background (G) or on a high-fat diet (H). For G, P < 0.05, n = 4; for H, P = NS, n = 3. HF, high fat; Wt, wild type. Pavlos Pissios et al. Diabetes 2007;56:311-319 ©2007 by American Diabetes Association