This study measures hexose monophosphate (HMP) shunt activity, glycolytic rate, and glucose transport in PMN and lymphocytes of patients with glycogen storage disease (GSD) type Ib as compared with controls and with GSD Ia patients. HMP shunt activity and glycolysis were significantly lower in intact PMN cells of GSD Ib patients as compared with GSD Ia patients and with controls. These activities were above normal levels in disrupted GSD Ib PMN. HMP shunt activity and glycolytic rates in lymphocytes were similar in all three groups studied. The rate of 2-deoxyglucose transport into GSD Ib PMN was 30% of that into cells of normal controls. In GSD Ib lymphocytes or in GSD Ia PMN and lymphocytes transport was normal. The striking limitation of glucose transport across the cell membrane of the PMN of GSD Ib patients may account for the impairment of leukocyte function that is characteristic of GSD Ib, but not found in GSD Ia patients.
N Bashan, Y Hagai, R Potashnik, S W Moses
Title and authors | Publication | Year |
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G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction
B Hayee, A Antonopoulos, EJ Murphy, FZ Rahman, G Sewell, BN Smith, S McCartney, M Furman, G Hall, SL Bloom, SM Haslam, HR Morris, K Boztug, C Klein, B Winchester, E Pick, DC Linch, RE Gale, AM Smith, A Dell, AW Segal |
Glycobiology | 2011 |
Long term G-CSF-induced remission of ulcerative colitis-like inflammatory bowel disease in a patient with glycogen storage disease Ib and evaluation of associated neutrophil function
A Alsultan, RJ Sokol, MA Lovell, G Thurman, DR Ambruso |
Pediatric Blood & Cancer | 2010 |
Unusual Oral Manifestations and Evolution in Glycogen Storage Disease Type Ib
C Mortellaro, U Garagiola, V Carbone, F Cerutti, V Marci, PL Bonda |
Journal of Craniofacial Surgery | 2005 |
Amelioration of Neutrophil Membrane Function Underlies Granulocyte-Colony Stimulating Factor Action in Glycogen Storage Disease 1b
E Lesma, E Riva, M Giovannini, AM Giulio, A Gorio |
International journal of immunopathology and pharmacology | 2005 |
Atlas of Metabolic Diseases Second edition
W Nyhan, B Barshop, P Ozand |
Atlas of Metabolic Diseases Second edition | 2005 |
Membrane Transporter Diseases
S Bröer, CA Wagner |
2003 | |
Association of glycogen storage disease 1b and Crohn disease: results of a North American survey
BK Dieckgraefe, JR Korzenik, A Husain, L Dieruf |
European Journal of Pediatrics | 2002 |
The glucose-6-phosphatase system
E Schaftingen, I Gerin |
Biochemical Journal | 2002 |
Granulocyte–Macrophage Colony-Stimulating Factor for Treating Gastrostomy Tube Site Healing in a Child With Glycogen Storage Disease Type Ib
BA Steinmetz, MG Martin, RL Roberts |
Journal of Pediatric Gastroenterology and Nutrition | 2001 |
Glucose-6-Phosphatase Mutation G188R Confers an Atypical Glycogen Storage Disease Type 1b Phenotype
BW Weston, JL Lin, J Muenzer, HS Cameron, RR Arnold, HH Seydewitz, E Mayatepek, EV Schaftingen, M Veiga-Da-Cunha, D Matern, YT Chen |
Pediatric Research | 2000 |
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I
G Visser, JP Rake, J Fernandes, P Labrune, JV Leonard, S Moses, K Ullrich, GP Smit |
The Journal of Pediatrics | 2000 |
A Convenient Diagnostic Function Test of Peripheral Blood Neutrophils in Glycogen Storage Disease Type Ib
AJ Verhoeven, G Visser, RV Zwieten, B Gruszczynska, DW Poll-The, GP Smit |
Pediatric Research | 1999 |
Principles of Perinatal—Neonatal Metabolism
RM Cowett |
1998 | |
Treatment of Chronic Enteritis in Glycogen Storage Disease Type IB with Granulocyte Colny-Stimulating Factor
EG Hoover, JJ DuBois, TL Samples, JS McCullough, PJ Chenaille, RG Montes |
Journal of Pediatric Gastroenterology & Nutrition | 1996 |
Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b
J Levy, MT Abu-Ras, T Berenstein, R Potashnik, I Meisner, SW Moses, N Bashan |
Journal of Inherited Metabolic Disease | 1994 |
Defective neutrophil and monocyte functions in glycogen storage disease type Ib: A literature review
R Gitzelmann, NU Bosshard |
European Journal of Pediatrics | 1993 |
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patients
N Bashan, R Potashnik, A Peist, N Peleg, A Moran, SW Moses |
European Journal of Pediatrics | 1993 |
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b
HM Korchak, , CA Stanley, L Baker, SD Douglas, L Kilpatrick |
European Journal of Pediatrics | 1993 |
Brain abscesses in glycogen-storage disease-type 1b
BZ Garty, A Rachmel, H Mandel, M Nitzan |
Acta Paediatrica | 1992 |
Chronic inflammatory bowel disease in glycogen storage disease type 1B
IR Sanderson, WM Bisset, PJ Milla, JV Leonard |
Journal of Inherited Metabolic Disease | 1991 |
Brain Abscess in Glycogen Storage Disease Type Ib
HK Park, SG Kahler, YT Chen |
Acta Paediatrica | 1991 |
Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type Ib
H Schroten, J Roesler, T Breidenbach, U Wendel, J Elsner, S Schweitzer, C Zeidler, S Burdach, ML Lohmann-Matthes, V Wahn, K Welte |
The Journal of Pediatrics | 1991 |
Impaired metabolic function and signaling defects in phagocytic cells in glycogen storage disease type 1b
L Kilpatrick, BZ Garty, KF Lundquist, K Hunter, CA Stanley, L Baker, SD Douglas, HM Korchak |
Journal of Clinical Investigation | 1990 |
Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b
N Bashan, R Potashnik, N Peleg, A Moran, SW Moses |
Journal of Inherited Metabolic Disease | 1990 |
Normal polymorphonuclear neutrophil function in a case of glycogen storage disease type Ib
E Bonioli, C Bellini, AD Stefano, A Costa, S Canini, F Patrone |
European Journal of Pediatrics | 1990 |
A Method for the Diagnosis of Glycogen Storage Disease Type Ib using Polymorphonuclear Leukocytes
N Bashan, R Potashnik, M Phillip, YS Shin, SW Moses |
Journal of Inherited Metabolic Disease | 1989 |