Sphingolipid de novo synthesis: its relevance to metabolic diseases and cell polarity

Similar documents
Nutrition and Age-Associated Inflammation :Role of Nutritional Intervention Simin Nikbin Meydani, DVM, PhD.

Supplementary Figure S1. Effect of Glucose on Energy Balance in WT and KHK A/C KO

Hmgcoar AGCTTGCCCGAATTGTATGTG TCTGTTGTAACCATGTGACTTC. Cyp7α GGGATTGCTGTGGTAGTGAGC GGTATGGAATCAACCCGTTGTC

Increased de novo ceramide synthesis and accumulation in failing myocardium

Gene Polymorphisms and Carbohydrate Diets. James M. Ntambi Ph.D

Cholesterol and Sphingolipids in Non-Alcoholic fatty liver disease.

BCM 221 LECTURES OJEMEKELE O.

Yifan Fan, Fujun Shi, Jing Liu, Jibin Dong, Hai H. Bui, David A. Peake, Ming-Shang Kuo, Guoqing Cao, Xian-Cheng Jiang

There is a relationship between sphingolipid de novo biosynthesis

Summary and concluding remarks

3-keto-Dihydrosphingosine is an Important Early Metabolite of Sphingolipid Biosynthesis

A Central Role of MG53 in Metabolic Syndrome. and Type-2 Diabetes

Phospholipids Metabolism

Development of Sphingosine Kinase Selective Inhibitors for Cancer Therapy

ANSC/NUTR 601 GENERAL ANIMAL NUTRITION Stearoyl-CoA desaturase, VLDL metabolism, and obesity


Quantitation of Sphingolipids in Tissue Extracts by LC/MS/MS

Sphingosine-1-phosphate signaling and cardiac fibrosis. Department of Physiology, Kanazawa University School of Medicine, Kanazawa, Japan

Metabolism of acylglycerols and sphingolipids. Martina Srbová

Supplementary Information. MicroRNA-33b knock-in mice for an intron of sterol regulatory

MEMBRANE LIPIDS I and II: GLYCEROPHOSPHOLIPIDS AND SPHINGOLIPIDS

Lecture 3 6/28/10. Membrane Lipids. Importance of Membranes. Categories of Lipids. Lipids: Chapter 20 Sections 4-7. ! Membranes are important in

Suppl. Table 1: CV of pooled lipoprotein fractions analysed by ESI-MS/MS

Lipoprotein Formation, Structure and Metabolism: Cholesterol Balance and the Regulation of Plasma Lipid Levels

Unit IV Problem 3 Biochemistry: Cholesterol Metabolism and Lipoproteins

Supplemental Material. Results

Novel Reduction of PCSK9 Expression: Mechanistic Insights into the Anti-Atherosclerotic & Hypolipidemic Effects of Heat Shock Protein 27

ANSC (NUTR) 618 LIPIDS & LIPID METABOLISM Membrane Lipids and Sphingolipidsd

Table S1. Quantitative RT-PCR primers

Lipid Metabolism Prof. Dr. rer physiol. Dr.h.c. Ulrike Beisiegel

Receptor-mediated activation of ceramidase activity initiates the pleiotropic actions of adiponectin

AAV-TBGp-Cre treatment resulted in hepatocyte-specific GH receptor gene recombination

Optimising. membranes

Chapter 1 The Lipid Droplet: a Dynamic Organelle, not only Involved in the Storage and Turnover of Lipids

Metabolism dysregulation induces a specific lipid signature of nonalcoholic steatohepatitis in patients

AdPLA ablation increases lipolysis and prevents obesity induced by high fat feeding or leptin deficiency

Cholesterol Metabolism

Chapter 26 Biochemistry 5th edition. phospholipids. Sphingolipids. Cholesterol. db=books&itool=toolbar

Is it really that simple? Alyssa Hasty, PhD Associate Professor Molecular Physiology and Biophysics

Supplementary Materials for

The role of apolipoprotein D in lipid metabolism and metabolic syndrome

Review. Yaron Ilan. Gastroenterology and Liver Units, Department of Medicine, Hadassah Hebrew University Medical Center, Jerusalem, Israel

Males- Western Diet WT KO Age (wks) Females- Western Diet WT KO Age (wks)

PHOSPHOLIPIDS METABOLISM. BY Dr. Walid Said Zaki Dr. Marwa Ali LECTURER OF BIOCHEMISTRY AND MOLECULAR BIOLOGY

Master class Biomolecular Sciences Molecular Cell Biology.

Control 7 d cold 7 d CL

a! b! c! Supplementary Fig. 1! Diameter (μm) S1P (LogM) U (LogM) enos! β-actin! Nogo-B! MLEC! nnos! β-actin!

Very-Long Chain Fatty Acid Biosynthesis

Lipids. Lipids: a Diverse group of chemicals. Storage Lipids: derivatives of fatty acids. 11/21/10

HSP72 HSP90. Quadriceps Muscle. MEF2c MyoD1 MyoG Myf5 Hsf1 Hsp GLUT4/GAPDH (AU)

number Done by Corrected by Doctor

Identification of Sphingolipid Metabolites That Induce Obesity via Misregulation of Appetite, Caloric Intake and Fat Storage in Drosophila

Supplementary Fig. 1 eif6 +/- mice show a reduction in white adipose tissue, blood lipids and normal glycogen synthesis. The cohort of the original

ALT (U/L) (Relative expression) HDL (mm) (Relative expression) ALT (U/L) (Relative expression)

Supplementary Figure 1.

LIPID METABOLISM. Sri Widia A Jusman Department of Biochemistry & Molecular Biology FMUI

Examination III PHRM 836 Biochemistry for Pharmaceutical Sciences II December 19, 2014

E3 ligase TRIM72 negatively regulates myogenesis by IRS-1 ubiquitination

BIOL212 Biochemistry of Disease. Metabolic Disorders - Obesity

Block A: Membrane Biology & Biochemistry. Lipid signalling and sphingolipid function

Supplementary Materials for

2.5. AMPK activity

Supplemental Information. Increased 4E-BP1 Expression Protects. against Diet-Induced Obesity and Insulin. Resistance in Male Mice

Supplementary Figure 1

Membrane Lipids & Cholesterol Metabolism

Supplementary Figures for TSC1 controls macrophage polarization to prevent inflammatory disorder by Linnan Zhu et al

Supplemental Figure 1. Western blot analysis indicated that MIF was detected in the fractions of

Biological role of lipids

Probe. Hind III Q,!&#12?R'!! /0!!!!D1"?R'! vector. Homologous recombination

Lipid/Lipoprotein Structure and Metabolism (Overview)

BIOL2005 WORKSHEET 2008

CHAPTER 28 LIPIDS SOLUTIONS TO REVIEW QUESTIONS

Supplemental Table 1. List of primers used for real time PCR.

1.5 ASK1KO fed. fasted 16 hrs w/o water. Fed. 4th. 4th WT ASK1KO N=29, 11(WT), ,5(ASK1KO) ASK1KO ASK1KO **** Time [h]

Supplemental Data. Short Article. ATF4-Mediated Induction of 4E-BP1. Contributes to Pancreatic β Cell Survival. under Endoplasmic Reticulum Stress

The use of mass spectrometry in lipidomics. Outlines

Expanded View Figures

Cholesterol metabolism. Function Biosynthesis Transport in the organism Hypercholesterolemia

CHAPTER 28 LIPIDS SOLUTIONS TO REVIEW QUESTIONS

Chapter 8. Functions of Lipids. Structural Nature of Lipids. BCH 4053 Spring 2001 Chapter 8 Lecture Notes. Slide 1. Slide 2.

Organochloride pesticides impaired mitochondrial function in hepatocytes and. aggravated disorders of fatty acids metabolism

Skeletal muscle lipid deposition and insulin resistance: effect of dietary fatty acids and exercise 1 3

Lipids. Lipids. Jiří Jonák and Lenka Fialová Institute of Medical Biochemistry, 1st Medical Faculty of the Charles University, Prague

NASH Bench to Bedside

By: Dr Hadi Mozafari 1

Supplementary Materials for

Familial Hypercholesterolemia

Effects of Infection and Inflammation on Lipid and Lipoprotein Metabolism: Mechanisms and

Elevated Serum Levels of Adropin in Patients with Type 2 Diabetes Mellitus and its Association with

Supplementary Figure S I: Effects of D4F on body weight and serum lipids in apoe -/- mice.

Figure 1. Effects of FGF21 on adipose tissue. (A) Representative histological. findings of epididymal adipose tissue (B) mrna expression of

Postn MCM Smad2 fl/fl Postn MCM Smad3 fl/fl Postn MCM Smad2/3 fl/fl. Postn MCM. Tgfbr1/2 fl/fl TAC

ZL ZDF ZDF + E2 *** Visceral (g) ZDF

Role of fatty acids in the development of insulin resistance and type 2 diabetes mellitus

PLASMA LIPOPROTEINS AND LIPIDS DETERMINATION OF PLASMA CHOLESTEROL AND TRIGLICERIDE LEVEL

B. Patient has not reached the percentage reduction goal with statin therapy

human epithelial cells were pretreated with control sirna (50 nm) or GSK-3β sirna (50 nm)

Supplementary Figure 1

Abdallah Q& Razi. Faisal

Lipid Metabolism. Remember fats?? Triacylglycerols - major form of energy storage in animals

Transcription:

Sphingolipid de novo synthesis: its relevance to metabolic diseases and cell polarity Xian-Cheng Jiang (shian-chen chiang) SUNY Downstate Medical Center

Cell plasma membrane Lipid rafts Sphingolipid = sphingomyelin, glycosphingolipid, and ceramide

Sphingolipid Biosynthesis Serine + Palmitoyl-CoA SPT 3-Ketosphinganine Sphingomyelin Lysosphingomyelin Diglyceride SMS Phosphatidylcholine Sphinganine Dihydroceramide Ceramide 3-Ketosphinganine reductase Ceramide synthase Ceramide-1-P Dihydroceramide desaturase Sphingosine S-1-P Kinase Sphingosine-1-P

Serine Palmitol-CoA transferase (SPT) 1. SPT has subunits: Sptlc1 and Sptlc2/Sptlc3. 2. Sptlc1 and Sptlc2 total gene knockouts are embryonic lethal.

Subtopics The relevance of plasma membrane sphingolipid changes to the metabolic diseases. The effect of adenovirus associated virus (AAV)- Cre-mediated liver SPT deficiency on lipoprotein metabolism. The effect of albumin-cre-mediated liver SPT deficiency on hepatocyte polarity.

Blood glucose (mg/dl) Plasma insulin (ng/ml) Body weight (g) Blood glucose (mg/dl) ) m a r g ( t h g i e W y d o B WT 60 50 40 30 20 10 Sptlc2 partial deficiency increases insulin sensitivity * * * * * * * * * 0 0 5 10 15 20 Time (Week) WT KO Sptlc2+/- 600 WT * Sptlc2+/- 500 400 300 200 100 * 0 0 50 100 150 200 * Time (min) * 150 WT Sptlc2+/- 100 50 * * * 4 WT Sptlc2+/- 3 2 1 * * * 0 0 10 20 30 40 50 60 70 Time (min) 0 0 10 20 30 40 50 60 70 Time after glucose injection (min)

Sptlc2 partial deficiency increases insulin receptor phosphorylation Phosphorylated insulin receptor levels (% of WT) WT Insulin Sptlc2+/- Insulin IR-P Liver IR β-actin 600 500 400 300 200 100 * WT Sptlc2+/- * * 0 Liver Adipose Muscle Li et al. MCB. 2012

Myeloid cell-specific Sptlc2 deficient mouse preparation B B B R RB R R R B R B Exon 1 2 3 4 WT B B B R RB R R R B R B Neo Sptlc2-Flox Exon 1 2 3 4 LysM-Cre Transgene Loxp B B B R RB R R R B R B B: BgIII; R: EcoRI 1 kb Exon 1 4

Myeloid cell-specific Sptlc2 deficiency decreases atherosclerotic lesions (in arch) Control Sptlc2 KO Chakraborty et al. JCI. 2013

Myeloid cell-specific Sptlc2 deficiency decreases atherosclerotic lesions (root and en face) Control Sptlc2 KO Control Sptlc2 KO Chakraborty et al. JCI. 2013

Summary (1) Sphingolipid de novo synthesis related with the development of metabolic diseases. Inhibition of sphingolipid de novo synthesis may prevent metabolic diseases.

Subtopics The relevance of plasma membrane sphingolipid changes to the metabolic diseases. The effect of adenovirus associated virus (AAV)- Cre-mediated liver Sptlc2 deficiency on lipid metabolism. The effect of albumin-cre-mediated liver Sptlc2 deficiency on hepatocyte polarity.

Liver-specific KO mouse preparation 1. AAV-Cre (for adult) 2. Albumin-Cre transgenic mice (for whole life) 3. Inducible-Cre (for adult)

AAV-Cre/Sptlc2-loxp mice

Liver-specific Sptlc2 KO mouse preparation (for adult) B B B R RB R R R B R B Exon 1 2 3 4 WT B B B R RB R R R B R B Neo Sptlc2-Flox Exon 1 2 3 4 AAV-Cre Loxp B B B R RB R R R B R B B: BgIII; R: EcoRI 1 kb Exon 1 4

Plasma lipid measurement in liver-specific Sptlc2 KO and WT mice (LC/MS/MS) ----------------------------------------------------------------------- Mice SM PC PC/SM Cer Sph S-1-P DHS-1-P (mm) (mm) (ng/ml) (ng/ml) (ng/ml) (ng/ml) ----------------------------------------------------------------------- WT 96+9 1759+97 18+2 1000+85 23+2 264+21 114+14 Sptlc2+/- 61+5* 2096+89* 32+5* 462+42* 31+1* 242+13 99+13 ----------------------------------------------------------------------- Value: mean+sd; n=4-5. SM, sphingomyelin; Cer, Ceramide; Sph, Sphingosine; S-1-P, Sphingosine-1-phosphate; DHS-1-P, Dihydroxylsphingosine-1-phosphate. *P<0.01.

Plasma lipid measurement after AAV-Cre injection AAV-lacZ AAV-Cre Change P value Cholesterol (mg/dl) 104 ± 7.5 116 ± 21 Phospholipid (mg/dl) 198 ± 17 211 ± 27 Triglyceride (mg/dl) 47 ± 8 50 ± 7 Sphingomyelin (mg/dl) 28± 5 19± 2-32% P < 0.01 Li et al. JBC 2009

Liver lipid measurement in liver-specific Sptlc2 KO and WT mice (LC/MS/MS) ------------------------------------------------------------------- Mice SM PC Cer Sph S-1-P DHS-1-P (mg/mg liver) (ng/mg liver) ------------------------------------------------------------------- WT 0.58+0.02 17+1 134+10 2.2+0.3 0.10+0.01 0.12+0.02 Sptlc2KO 0.42+0.01* 15+2 82+9* 1.8+0.2 0.11+0.02 0.13+0.01 ------------------------------------------------------------------- Value: mean+sd; n=4-5. SM, sphingomyelin; PC, phosphatidylchline; Cer, ceramide; Sph, sphingosine; S-1-P, sphingosine-1-phosphate; DHS-1-P, dihydroxyl-sphingosine-1-phosphate. *P<0.01.

Plasma AAV-LacZ AAV-Cre

Sphingomyelin (OD600) Plasma sphingomyelin distribution Non-HDL HDL 0.20 0.15 WT Sptlc2 KO 0.10 0.05 0.00 0 5 10 15 20 25 30 35 Fractions Li et al. JBC 2009

Summary (2) As expected that AAV-Cre-mediated liver Sptlc2 deficiency decreases plasma sphingomyelin levels.

Subtopics The relevance of plasma membrane sphingolipid changes to the metabolic diseases. The effect of adenovirus associated virus (AAV)- Cre-mediated liver Sptlc2 deficiency on lipoprotein metabolism. The effect of albumin-cre-mediated liver Sptlc2 deficiency on hepatocyte polarity.

Albumin-Cre/Sptlc2-loxp mice

Liver-specific Sptlc2 KO mouse preparation (for whole life) B B B R RB R R R B R B Exon 1 2 3 4 WT B B B R RB R R R B R B Neo Sptlc2-Flox Exon 1 2 3 4 Albumin-Cre Transgene Loxp B B B R RB R R R B R B B: BgIII; R: EcoRI 1 kb Exon 1 4

SPT activity (% of WT) Liver SPT activity and Sptlc1/Sptlc2 protein mass in liver-specific Sptlc2 KO mice Control Sptlc2+/- Sptlc2-/- Sptlc2 Sptlc1 GAPDH 120 100 80 60 40 20 0 WT-Alb-Cre * Sptlc2-loxP/loxP-Alb- Cre

Bile ducks are few in Sptlc2 KO mouse liver (H&E staining, 2 months old) Control Hetero KO Homo KO

Bile ducks are few in Sptlc2 KO mouse liver (H&E staining, 2 months old) Control Sptlc2 KO

Reticular Fiber Staining for liver fibrosis (2 months old) WT Hetero KO Homo KO Silver staining (silver nitrate) ----Gordon-Sweets Method

Sptlc2 deficiency does not cause lipid accumulation in the liver (2 months old) Liver Oil red O staining Control Sptlc2 KO

Sptlc2-deficiency-mediated liver tumor formation (8 months old) Control Sptlc2 KO

Plasma lipid measurement (2 months old) WT Homozygous KO Heterozygous KO Cholesterol (mg/dl) 80 ± 6 354 ± 59* 77 ± 14 Phospholipid (mg/dl) 217 ± 10 746 ± 19* 173 ± 44 Sphingomyelin (mg/dl) 14 ± 2 44 ± 10* 12 ± 2 Triglyceride (mg/dl) 56 ± 8 69 ± 10 58 ± 9

Phospholipids (OD600) Triglycerid (OD490) Sphingomyelin (OD600) Cholesterol (OD600) Plasma lipid distribution (FPLC) (chow diet) 0.5 0.4 0.3 0.2 0.1 WT Sptlc2+/- Sptlc2-/- Non-HDL 0.0 0 5 10 15 20 25 30 35 Fractions HDL 0.7 0.6 0.5 0.4 0.3 0.2 0.1 WT Sptlc2+/- Sptlc2-/- 0.0 0 5 10 15 20 25 30 35 Fractions 1.5 WT Sptlc2+/- Sptlc2-/- 0.5 0.4 WT Sptlc2+/- Sptlc2-/- 1.0 0.3 0.5 0.2 0.1 0.0 0 5 10 15 20 25 30 35 Fractions 0.0 0 5 10 15 20 25 30 35 Fractions

Higher cholesterol in liver Sptlc2 KO mice has no impact on atherosclerosis WT Sptlc2 KO

Liver Sptlc2 KO mice have severe jaundice Control Sptlc2 +/- Sptlc2 -/-

Cholestasis Cholestasis is a condition where bile cannot flow from the liver to the duodenum. 1. Gallstone or malignance 2. Genetic defects

Plasma Bilirubin (mg/dl) Plasma Bilirubin 9 8 7 6 5 4 3 2 1 0 * * WT-Alb-Cre Sptlc2-loxp/loxp-Alb-Cre * Total Direct Indirect

EM picture for lipoprotein-x Felker et al. PNAS, 1978

Accumulation of lipoprotein-x in Sptlc2 KO mouse plasma Control Sptlc2 KO

Sptlc2 KO mice have much less microvilli in bile canaliculus Control Sptlc2 KO

Bile flow rate (ul/min/100 g body weight) Liver Sptlc2 deficiency dramatically decreases flow rate of bile Control KO 2.5 2 1.5 1 0.5 * 0 WT Sptlc2-loxp/loxp-Alb-Cre Collect bile for 1 hr

Hepatocyte polarity

Bile production ABCA1 (ABCB11) (ABCB4)

Sptlc2 KO mice lose hepatocyte polarity ABCB11 ABCA1 Merge Control KO

Sptlc2 KO mice lose hepatocyte polarity (Filipin staining) Control Sptlc2 KO

Comparison between liver LKB1 KO and liver Sptlc2 KO mice LKB1-Flox/albumin-Cre (Woods et al. BJ 2011) LpX accumulation in the blood Defective targeting of ABCB11 Jaundice Abnormal bile canaliculus Died at age 30 days Sptlc2-Flox/albumin-Cre LpX accumulation in the blood Defective targeting of ABCB11 Jaundice Abnormal bile canaliculus Normal life span with liver tumors Above abnormalities do not exist in AdV-Cre-mediated LKB1 liver deficiency (Shaw et al. Science, 2005) and AAV-Cre-mediated Sptlc2 liver deficiency (Li et al. JBC, 2009).

Sphingomyelin Biosynthesis Serine + Palmitoyl-CoA SPT 3-Ketosphinganine Sphingomyelin Lysosphingomyelin myriocin Fumonisin B1 Diglyceride SMS Phosphatidylcholine Sphinganine Dihydroceramide Ceramide 3-Ketosphinganine reductase Ceramide synthase Ceramide-1-P Dihydroceramide desaturase Sphingosine S-1-P Kinase Sphingosine-1-P

Myriocin treatment attenuates LKB1 activation Primary hepatocytes 0 50 100 200 Myriocin µm P-LKB1 GAPDH Huh7 Cells 0 50 100 200 Myriocin μm P-LKB1 GAPDH

Fumonisin B1 treatment attenuates LKB1 activation in primary hepatocytes 0 50 Fumonisin B1 μm P-LKB1 GAPDH

Ceramide treatment attenuates LKB1 activation in primary hepatocytes Primary hepatocytes 0 5 10 20 Ceramide μm P-LKB1 GAPDH Huh7 Cells 0 10 30 Ceramide µm P-LKB1 GAPDH

Sphingomyelin treatment promotes LKB1 activation Huh7 Cells 0 10 30 Sphingomyelin µm P-LKB1 GAPDH

Summary (3) In the early stage of life, Sptlc2 is involved in the formation of liver cell polarity. In adult livers, cell polarity formation would have progressed normally through development. Sptlc2 deficiency in adulthood do not influence cell polarity. Both LKB1 and Sptlc2 deficiencies in the liver have similar phenotype, in terms of cell polarity. Do LKB1 and Sptlc2 have a linkage?

LKB1: cell polarity and metabolism Hezel and Bardeesy, 2008

Questions: Sphingolipid de novo synthesis Where? membrane? Which factors? PKCs?

Enterocyte polarity Tight junction Basal lamina

Macrophage polarity

Mahua Zhiqiang Jiang

Acknowledgement Downstate Medical Center Zhiqiang Li Mahua Chakraborty Chongmin Huan Inamul Kair Gachon University of Medicine and Science Tae-Sik Park Eli Lilly & Company Ming-Shang Kuo Guoqing Cao