Artificial liver in PKU. Donna Santillan, PhD University of Iowa Hospitals & Clinics Department of Obstetrics & Gynecology

Similar documents
Chapter 1: What is PKU?

Cell encapsulation as a potential non-dietary therapy for maternal phenylketonuria

PKU PKU. Phenylketonuria TEMPLE. Information for families following Information for families after a positive newborn screening

Amal Alamri. Phenylketonuria

TEMPLE. Tools Enabling Metabolic Parents LEarning ADAPTED BY THE DIETITIANS GROUP. British Inherited Metabolic Diseases Group

PKU, a genetic disease, illustrating the principle:

Recent Studies of Phenylketonuria By: Jennifer Gastelum Dr. Koni Stone Copyright 2014

Phenylketonuria (PKU) the Biochemical Basis. Biol 405 Molecular Medicine

PHENYLKETONURIA. Debbie Galo

Lab Activity 36. Principles of Heredity. Portland Community College BI 233

PAH phenylalanine + oxidant tyrosine CH 2 +H 3 N

Prerequisites Amino acid synthesis and degradation pathways. Integration of amino acid metabolic pathways with carbohydrate metabolic pathways.

Screening for Phenylketonuria: A Literature Update for the U.S. Preventive Services Task Force

Research Article The Association between EEG Abnormality and Behavioral Disorder: Developmental Delay in Phenylketonuria

BAHAN AJAR IV Phenylketonurias (Phenylalanine Hydroxylase Deficiency) Nama Mata Kuliah/Bobot SKS : Sistem Neuropsikiatri / 8 SKS

Testing for Genetic Disorders that Cause Brain Damage

Therapeutic Programming of Synthetic Biotic Medicines

A. We are constantly being tested (from birth). 1) Why? Test newborns to check for congenital health problems. 2) What does congenital mean?

Pathophysiology of the Phenylketonuria

Summary comments: An essential pattern employed by all living things: DNA ö RNA ö Protein

PKU TEMPLE. Tools Enabling Metabolic Parents LEarning ADAPTED AND ENDORSED BY ASIEM FOR USE IN ANZ DESIGNED AND ADAPTED BY THE DIETITIANS GROUP

University Journal of Pre and Paraclinical Specialities

PKU, KUVAN, and You PKU treatment and support for adults and young adults

PKU (Phenylketonuria) Serum HPLC Analysis Kit User Manual

Human inherited diseases

ESPEN Congress Madrid 2018

THE KING AND THE SCRATCHED DIAMOND

PKU (Phenylketonuria) Serum LC-MS/MS Analysis Kit User Manual

Most common metabolic disorders in childhood. Neonatal screening and diagnostic approach to the. Inborn errors of metabolism (IEM)

- Aya Alomoush. - Talal Al-Zabin. - Belal Azab. 1 P a g e

THBA Platform - Bile acid imbalance

Summary. Syndromic versus Etiologic. Definitions. Why does it matter? ASD=autism

Metabolic Disorders. Chapter Thomson - Wadsworth

1 Cognitive, Psychological and Behavioral Assessment Based Evidence

HEREDITARY METABOLIC DISEASES

7 Medical Genetics. Hemoglobinopathies. Hemoglobinopathies. Protein and Gene Structure. and Biochemical Genetics

Phenylalanine. in cases of hyperphenylalaninemia and tetrahydrobiopterin deficiency

Phenylketonuria Jonathan Baghdadi and Evan Marlin

Guided Notes: Simple Genetics

BEHAVIORAL ASSESMENT OF THE Pah enu2 MOUSE MODEL OF PHENYLKETONURIA PADMINI ASHOK KUMAR

INVESTIGATION THE PREVALENCE OF MUTATIONS IVS 10 AND R158Q IN A NUMBER OF IRANIAN PATIENTS WITH PKU

Boston Children s Hospital Transition Toolkit

2015 PKU Patient Survey Results. National PKU Alliance PO Box 501, Tomahawk, WI

number Done by Corrected by Doctor

PKU, KUVAN, and Your Child Making smart choices for PKU treatment

Genetic Disorders. Students must provide an explanation for all problems. Students must have parent signature prior to submission.

Not intended for UK based media. Merck Announces Detailed 26-Week Results from Phase IIIb Study with Kuvan in children with PKU below 4 years of age

Thin-Layer Chromatography of Amino Acids HASPI Medical Biology Lab 15b Background Macromolecules

Newborn Screening: Blood Spot Disorders

Manual. Transfer step. Figure 1. Workflow comparison of manual phenylalanine assay and automated GSP Neonatal Phenylalanine assay

<10. IL-1β IL-6 TNF + _ TGF-β + IL-23

Genetics Unit Exam. Number of progeny with following phenotype Experiment Red White #1: Fish 2 (red) with Fish 3 (red) 100 0

Two Siblings of Hyperphenylalaninemia: Suggestion to a Genetic Variant of Phenylketonuria

Chapter 28 Modern Mendelian Genetics

Psych 3102 Lecture 3. Mendelian Genetics

Attachment 1. Newborn Screening Program Description

Tay Sachs, Cystic Fibrosis, Sickle Cell Anemia and PKU. Tay Sachs Disease (also called Hexosaminidase deficiency)

Human Genetic Diseases (non mutation)

The National Society for Phenylketonuria (United Kingdom) Ltd. The Child with PKU. Brenda Clark Professor Forester Cockburn Dr Linda Tyfield

High-Absorbable Ferric Pyrophosphate for Iron Supplement. Ferrsorb

Biology 12. Mendelian Genetics

Solutions to Genetics Unit Exam

Adult PKU. Important Information for You. Mead Johnson Metabolics

MyBaby & PKU. 1) MyBaby s diagnosis. newborn screening. call from Sick Kids. visit to PKU clinic at Sick Kids test results

Contemporary Nutrition

INBORN ERRORS OF METABOLISM (IEM) IAP UG Teaching slides

Chapter 10 FROM PROTEINS TO PHENOTYPES

YOU ARE WHAT YOU EAT. What are some of the biggest nutritionrelated threats the world faces today?

Low Therapeutic Threshold for Hepatocyte Replacement in Murine Phenylketonuria

A. History Urinalysis is the oldest lab test still being performed today

Amino Acid Disorders. Disorder name: Tyrosinemia, type 1. What is tyrosinemia 1? Genetic Fact Sheets for Parents

Instructions. Fuse-It-mRNA easy. Shipping and Storage. Overview. Kit Contents. Specifications. Note: Important Guidelines

Cystic Fibrosis. Parkland College. Monica Rahman Parkland College. Recommended Citation

Featured Topic: Natural Help for Leaky Bladders (5 slides)

PEPTIDES and PROTEINS

Research Shows Healthy Living is Longer Living

Peptides and Proteins:

11: Pathways. Reminders:

HA Convention 2016 Master course How to Handle Abnormal Newborn Metabolic Screening Results Causes, Management and Follow up

Electron micrograph of phosphotungstanic acid-stained exosomes derived from murine

Information for health professionals

Annual Conference. 34th. The Rendezvous Hotel Skipton, Yorkshire. Welcome to. Programme Information & Abstracts

For research or further manufacturing use only. Not for injection or diagnostic procedures.

Merck KGaA, Darmstadt, Germany, Receives EU-Approval to Extend Kuvan Use to Children with PKU Below 4 Years of Age

Molecules. Background

Untitled Document. 1. Which of the following is the template for the production of RNA within a cell? A. DNA B. ATP C. protein D.

3. Mating two organisms produces a 3:1 ratio of the phenotype in progeny. The parental genotypes are

Table of Contents Preface...1 What is PKU?...2 Where does PKU come from?...3 How is PKU Treated?...4 Controlling Blood Phe *...5 Phenyl-Free How

Section Objectives: Pedigrees illustrate inheritance. Pedigrees illustrate inheritance

Station One: Nutrition

Chapter 20. Assisting With Nutrition and Fluids

Enteral and parenteral nutrition in GI failure and short bowel syndrome

Genetics All somatic cells contain 23 pairs of chromosomes 22 pairs of autosomes 1 pair of sex chromosomes Genes contained in each pair of chromosomes

Disclosure. I have no disclosures to mention

Nutritional Management of Inborn Errors of Metabolism. Kay Davis, RD, CSP Esther Berenhaut, RD, CSP, CSR Aug 28, 2017

2.1 Reproduction At the end of this sequence of lessons I can:

INTEGRATION OF GENERAL AMINO ACID CONTROL AND TOR REGULATORY PATHWAYS IN NITROGEN ASSIMILATION IN YEAST

Inheritance of Aldehyde Oxidase in Drosophila melanogaster

Molecular Genetics and Metabolism

Transcription:

Artificial liver in PKU Donna Santillan, PhD University of Iowa Hospitals & Clinics Department of Obstetrics & Gynecology

Discovery of PKU Discovery of PKU Discovered in 1934 by Dr. Asbjörn Fölling Egeland family asked if children s urine odor was related to their mental retardation Studied urine samples from children Turned dark green when mixed with ferric chloride Isolated phenylpyruvic acid

Discovery of PKU Discovery of PKU Borgny & Harry Egeland and their 2 children. Tested 430 institutionalized children 8 had the same abnormality (2 sibling pairs) Dr. Penrose later named the disease phenylketonuria after the characteristic presence of the phenylketone, phenylpyruvic acid in the urine. 1950s diet food developed 1960s testing infants became common

Phenylketonuria (PKU) Autosomal recessive disorder Classic form due to inactivation of Pah Over 500 cataloged mutations Major biosynthetic route to tyrosine Cannot metabolize phenylalanine Phe makes up 5% of protein foods Significant buildup of phenylketones in bloodstream Mental retardation (IQ<30), skin rashes, seizures, excessive restlessness, irritable behavior Dietary Therapy Formula foods Stringent, foul tasting, expensive

Phenylalanine hydroxylase (PAH) PAH gene located on chromosome 12 Converts Phenylalanine to tyrosine in the presence of BH4 co-factor

How do you cure PKU? Liver Transplant

Cell Transplant: Domino Donor Infusion of transplanted liver cells using a transcutaneous portal catheter Cells from explanted liver of 14mo old with type Ib glycogen storage disease First series: 2 infusions over 2 days (viability: 82% day 1, 78% day 2) Second series: donor cells from male cadaver (viability 82%) Effects lasted 3 months Accepted 1/5/12 epub provisional 10/8/2011 Cell Transplantation

Domino transplant: Blood Phe We conclude that cell transplantation for PKU patients is an option that may correct severe hyperphenylalaninemia in poorly controlled patients being at high risk of neurologic and intellectual impairment.

How to overcome the Immune System Protect cells (native or genetically engineered) from ever being exposed to the immune system. Encapsulate cells within semipermeable microspheres

Hypothesis Injection of encapsulated cells which express Phenylalanine Hydroxylase (PAH) that can function as an artificial liver can reduce serum Phe levels and reverse disease characteristics.

Can a non-dietary therapy reverse phenotypic changes? Goal: Develop an effective long acting non-dietary therapy.

Cell Encapsulation Tyrosine, Toxins Cells Allografts (Other Humans) Xenografts (Animals) Biocompatible Material Cell Immune cells, Antibodies Nutrients, Phenylalanine Biocompatible Material

Cell encapsulation for PKU O 2 Nutrients Phenylalanine Tyrosine Immune system cells Alginate membrane PAH expressing cells Immunoglobulin Based on an image at http://www.mitr.p.lodz.pl/biomat/raport/4_9_radiation_hydrogels.html by J. Rosiak

Cell Encapsulation Cells & Alginate Air Cells are washed 2x in PBS and resuspended in 1.5% alginate Infusion pump at 59 ml/hr Air pushes droplets off Spheres polymerize upon contact with CaCl 2 solution Spheres filtered through 70 micron filter Grown under normal cell culture conditions or transplanted CaCl 2

Encapsulated Cells Optimize: Distance Cell concentration Air pressure Infuser pump speed Set up design 97.9 ± 20.0 microns n=41

Phe Measurement Plate cells and media Collect and freeze media samples Spot samples on Newborn Screening Cards Phe measured by Tandem Mass Spectrometry

Phe concentration in media [mg/dl] Phe [mg/dl] Does cell encapsulation affect the ability of cells to reduce Phe? 70 60 50 40 Mock PAH 30 20 * 10 0 Mock PAH PAH 50% reduction in Phe concentration (6 days post-transfection)

Do encapsulated cells remain viable over time? Cells encapsulated in microspheres dissolved in sodium citrate buffer to degrade alginate beads Cells stained with trypan blue and counted using hemocytometer

Cell Viability results in vitro Average percent cell viability ± SEM Days 293T cells WRL68 cells HepG2 cells 0 92.33 ± 1.45 89.33 ± 1.15 91.53 ± 1.34 4 89 ± 1.56 87.67 ± 1.53 90.2 ± 0.75 7 88.43 ± 1.54 85.33 ± 1.17 88.45 ± 1.24 14 86.2 ± 1.51 84.2 ± 1.63 86.86 ± 1.43 21 83.67 ± 1.83 81.76 ± 1.74 84.52 ± 1.78 28 79.32 ± 1.92 78.42 ± 2.12 82.79 ± 1.49 Cell viability remains high throughout 28 days of cell encapsulation.

How does PAH expression vary between cell lines? To determine mrna PAH expression levels in different cell lines by qrt-pcr RNA was isolated from frozen cell pellets mrna expression levels of different cell lines were analyzed and compared Ct = expression

Expression Quantitative Real-Time PCR 30 Ave ΔCt 25 20 15 10 5 0 293T 293T clone 1 WRL68 HepG2 HepG2 cells express the highest level of PAH.

Who s Who of Mice Homozygous C57PAH enu2 = PKU (grey fur) Heterozygous C57PAH enu2 = no PKU (black fur)

Comparison of In Vivo Phe levels posttreatment Mole/L * * P<0.05 denoted by * Days Post Treatment

Analysis of survival Strain Treatment Survival at 28 days homozygous PAHenu2 empty spheres 5/5 heterozygous empty spheres 5/5 BTBR empty spheres 5/5 homozygous PAHenu2 encapsulated cells 5/5

In vivo cell viability: Day 28 Day 0 post-encapsulation: 88% Mouse Percent cell viability 1 83.3 2 80 3 72.9 4 85 5 79.4 6 74.2 7 84.7

Understanding the PKU mouse model is critical to testing effects of therapies. Coloring Fertility Metabolism Sleep Immune System

Hypothesis Lowering Phe in mice will correct other characteristics found in homozygous (PKU) mice. There is more to know than Phe levels!

Phenotypic Correction: HepG2 DAY 0 Treated male homozygous PKU mouse Untreated male wild type mouse DAY 28 Female mouse: Delivered 5 pups Day 1: 1.1 ± 0.06g Wild type mouse Treated male homozygous PKU mouse

PKU mice are smaller than their counterparts.

What is the root cause of the difference? INPUT OUTPUT Food Intake Food Composition Digestive Efficiency Heat Production Physical Activity

What are the ins & outs in PKU mice? Group Heterozygous Female (n=7) Homozygous Female (n=8) Food Intake (grams/day) Fluid Intake (ml/day) Urine Output (grams/day) 3.72 2.97 0.35 1.16 4.47 5.39 1.72 1.46 Heterozygous Male (n=7) 3.28 2.95 0.33 1.00 Homozygous Male (n=6) 4.41 4.37 1.13 1.41 Fecal Output (grams/day) PKU mice eat more, drink more, make more urine and feces. PKU mice lose more calories through feces, but this is not made up for by the increased food smaller mice.

What are the ins & outs in treated PKU mice? Group Heterozygous Female (n=7) Homozygous Female (n=8) Food Intake (grams/day) Fluid Intake (ml/day) Urine Output (grams/day) 3.72 2.97 0.35 1.16 3.87 2.23 1.24 0.98 Heterozygous Male (n=7) 3.28 2.95 0.33 1.00 Homozygous Male (n=6) 2.89 1.8 0.93 0.835 Fecal Output (grams/day) PKU mice eat more, drink more, make more urine and feces Corrected in treated PKU mice.

The artificial liver reverses the increase in caloric intake and absorption. Group Food Intake Σ kcal/day Fecal Output Σ kcal/day Absorbed Σ kcal/day Heterozygous 13.17 2.67 10.49 Homozygous 18.59 4.00 14.58 Homozygous - treated 15.05 3.04 12.01 16 Absorbed Total kcal/day 14 12 10 8 6 4 2 0 Heterozygous Homozygous Treated

Are there basic differences in resting metabolic rate in PKU mice?

Artificial liver starts to relieve the sleep disorder in females.

Dendritic Cells B Cells NK Cells T Cells Immune system changes also begin to correct. Heterozygous Homozygous Treated Homozygous CD4+ Total 14.6 ±0.9 18.7 ±5.4 18.5 ±4.9 CD4+ Naïve 72.4 ±2.1 65.2 ±6.1 68.4 ±4 CD4+ Memory 9.4 ±4.3 9.8 ±3.6 10.7 ±2.8 CD8+ Total 10.1 ±1.5 12.7 ±2.6 8 ±4.1 CD8+ Naïve 32.6 ±3.7 28.8 ±4.1 27.7 ±2.5 CD8+ Memory 17.3 ±2.5 20 ±1.2 16.4 ±4.4 NK1.1+ 3.6 ±0.5 4.7 ±1.6 3.6 ±1.6 B220+ Total 56.7 ±2.2 47.1 ±7.6 47.6 ±4.5 B220+ CD80+ 87.7 ±13.3 32.7 ±18.1 84.8 ±18 B220+ CD86+ 5.5 ±4.2 5.8 ±1.9 7.5 ±1.8 B220+ IgM+ 47.9 ±15.2 56.9 ±4.3 59.7 ±6.7 CD11c+ Total 2.7 ±0.6 4.0 ±0.5 3.7 ±1.1 CD11c+ CD80+ 78.0 ±9.6 39.4 ±8.9 61.2 ±16.1 CD11c+ CD86+ 72.5 ±5.6 21.6 ±2.8 73.3 ±8.9

Who s who in the immune system B cells make antibodies and stimulate other immune system cells

Who s who in the immune system Dendritic cells process and present infections to stimulate other immune system cells

MFI MFI Mean Fluorescence Intensity Mean Fluorescence Intensity Heterozygous Homozygous Treated Homozygous MFI MFI Mean Fluorescence Intensity Mean Fluorescence Intensity MFI MFI Mean Fluorescence Intensity Mean Fluorescence Intensity N=4 * = p<0.05, ** = p<0.01 150 150 100 100 50 50 0 0 p=0.0524 B Cells CD40 CD80 CD86 * 5000 5000 HET 4000 HOMO HOMO+Spheres 3000 4000 3000 2000 2000 1000 1000 0 0 p=0.0804 p=0.0804 150 150 HET HOMO HOMO+Spheres 100 100 50 50 0 0 150 150 100 100 Dendritic Cells CD40 CD80 CD86 p=0.0640 3000 3000 HET HOMO 2000 HOMO+Spheres 2000 ** ** * * 3000 3000 HET HOMO HOMO+Spheres 2000 2000 * * ** ** 50 50 1000 1000 1000 1000 0 0 0 0 0 0

Summary Hepatocyte cell lines express high levels of PAH Encapsulating cells does not prevent processing of Phe Encapsulated cells reduce Phe in vitro and in vivo Phenotypic correction can be observed in treated PKU model mice Change in fur color Change in fertility Changes in Food intake and absorbed calories Changes in sleep Changes in B cells and Dendritic cells

Conclusion Cell transplantation with encapsulated PAH expressing cells holds potential has a non-dietary therapy for PKU syndrome.

Acknowledgements Stephen Hunter, MD, PhD Brenda Boese Eric Devor, PhD Justin Grobe, PhD Nicole Pearson, MS Mark Santillan, MD Sabrina Scroggins, PhD Ben Weidemann Anita Xavier, MS Department of Obstetrics & Gynecology, University of Iowa Newborn Screening Lab, University of Iowa Hygienic Lab National Institutes of Health (R01 to SH) Iowa PKU Foundation

National PKU Alliance