Epo is relevant neither for microvascular formation nor for the new formation and maintenance of mice skeletal muscle fibres in both normoxia and hypoxia

Journal of Biomedicine and Biotechnology

Volumn 2010, Issue , 2010, Pages

  Launay, Thierry ^a,c   Hagström, Luciana ^a   Agbulut, Onnik ^b   El Hasnaoui Saadani, Raja ^a   Marchant, Dominique ^a   Favret, Fabrice ^a   Richalet, Jean Paul ^a   Beaudry, Michèle ^a  

^a UNIVERSITÉ PARIS 13   (France)

^b Groupe Hospitalier Pitié Salpêtrière   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROPOIETIN; ERYTHROPOIETIN RECEPTOR; HYPOXIA INDUCIBLE FACTOR 1ALPHA; UNCLASSIFIED DRUG; VASCULOTROPIN; VASCULOTROPIN 120; VASCULOTROPIN RECEPTOR 2; HYPOXIA INDUCIBLE FACTOR 1;

ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BODY WEIGHT; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; GASTROCNEMIUS MUSCLE; HEMATOCRIT; HYPOXIA; IMMUNOHISTOCHEMISTRY; KIDNEY FAILURE; MALE; MOUSE; MUSCLE ATROPHY; MUSCLE MASS; NONHUMAN; NUCLEOTIDE SEQUENCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SARCOMERE LENGTH; SKELETAL MUSCLE; TRANSGENIC MOUSE; UPREGULATION; ANALYSIS OF VARIANCE; ANIMAL; ANOXIA; BLOOD; CHEMISTRY; CYTOCHEMISTRY; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MICROVASCULATURE; NONPARAMETRIC TEST; PHYSIOLOGY; SARCOMERE; VASCULARIZATION;

MUS; MUS MUSCULUS;

ANALYSIS OF VARIANCE; ANIMALS; ANOXIA; ERYTHROPOIETIN; HISTOCYTOCHEMISTRY; HYPOXIA-INDUCIBLE FACTOR 1; MALE; MICE; MICE, TRANSGENIC; MICROVESSELS; MUSCLE FIBERS, SKELETAL; MUSCLE, SKELETAL; MUSCULAR ATROPHY; NEOVASCULARIZATION, PHYSIOLOGIC; RECEPTORS, ERYTHROPOIETIN; SARCOMERES; STATISTICS, NONPARAMETRIC; UP-REGULATION; VASCULAR ENDOTHELIAL GROWTH FACTORS;

EID: 77952483216     PISSN: 11107243     EISSN: 11107251     Source Type: Journal    
DOI: 10.1155/2010/137817     Document Type: Article

References (47)

1. Li F., Chong Z. Z., Maiese K., Erythropoietin on a tightrope: balancing neuronal and vascular protection between intrinsic and extrinsic pathways Neurosignals 2004 13 6 265 289
2. Bozzini C. E., Enhanced erythropoietin production during hypobaric hypoxia in mice under treatments to keep the erythrocyte mass from rising: implications for the adaptive role of polycythemia High Altitude Medicine and Biology 2005 6 3 238 246
3. Abbrecht P. H., Littell J. K., Erythrocyte life-span in mice acclimatized to different degrees of hypoxia Journal of Applied Physiology 1972 32 4 443 445
4. Richalet J. P., Souberbielle J. C., Antezana A. M., Control of erythropoiesis in humans during prolonged exposure to the altitude of 6,542m American Journal of Physiology 1994 266 3, part 2 R756 R764
5. Witthuhn B. A., Quelle F. W., Silvennoinen O., JAK2 associates with the erythropoietin receptor and is tyrosine phosphorylated and activated following stimulation with erythropoietin Cell 1993 74 2 227 236
6. Jelkmann W., Erythropoietin after a century of research: younger than ever European Journal of Haematology 2007 78 3 183 205
7. Ogilvie M., Yu X., Nicolas-Metral V., Erythropoietin stimulates proliferation and interferes with differentiation of myoblasts Journal of Biological Chemistry 2000 275 50 39754 39761
8. Lundby C., Hellsten Y., Jensen M. B. F., Munch A. S., Pilegaard H., Erythropoietin receptor in human skeletal muscle and the effects of acute and long-term injections with recombinant human erythropoietin on the skeletal muscle Journal of Applied Physiology 2008 104 4 1154 1160
9. Rotter R., Menshykova M., Winkler T., Erythropoietin improves functional and histological recovery of traumatized skeletal muscle tissue Journal of Orthopaedic Research 2008 26 12 1618 1626
10. Jaquet K., Krause K., Tawakol-Khodai M., Geidel S., Kuck K.-H., Erythropoietin and VEGF exhibit equal angiogenic potential Microvascular Research 2002 64 2 326 333
11. Kertesz N., Wu J., Chen T. H.-P., Sucov H. M., Wu H., The role of erythropoietin in regulating angiogenesis Developmental Biology 2004 276 1 101 110
12. Suzuki N., Ohneda O., Takahashi S., Erythroid-specific expression of the erythropoietin receptor rescued its null mutant mice from lethality Blood 2002 100 7 2279 2288
13. El Hasnaoui-Saadani R., Pichon A., Marchant D., Cerebral adaptations to chronic anemia in a model of erythropoietin-deficient mice exposed to hypoxia American Journal of Physiology 2009 296 3 R801 R811
14. Poltorak Z., Cohen T., Sivan R., VEGF145, a secreted vascular endothelial growth factor isoform that binds to extracellular matrix Journal of Biological Chemistry 1997 272 11 7151 7158
15. Tischer E., Mitchell R., Hartman T., The human gene for vascular endothelial growth factor: Multiple protein forms are encoded through alternative exon splicing Journal of Biological Chemistry 1991 266 18 11947 11954
16. Ng Y.-S., Rohan R., Sunday M. E., Demello D. E., DAmore P. A., Differential expression of VEGF isoforms in mouse during development and in the adult Developmental Dynamics 2001 220 2 112 121
17. Robinson C. J., Stringer S. E., The splice variants of vascular endothelial growth factor (VEGF) and their receptors Journal of Cell Science 2001 114 5 853 865
18. Park J. E., Keller G.-A., Ferrara N., The vascular endothelial growth factor (VEGF) isoforms: differential deposition into the subepithelial extracellular matrix and bioactivity of extracellular matrix-bound VEGF Molecular Biology of the Cell 1993 4 12 1317 1326
19. Fahal I. H., Bell G. M., Bone J. M., Edwards R. H. T., Physiological abnormalities of skeletal muscle in dialysis patients Nephrology Dialysis Transplantation 1997 12 1 119 127
20. Kopple J. D., Storer T., Casburi R., Impaired exercise capacity and exercise training in maintenance hemodialysis patients Journal of Renal Nutrition 2005 15 1 44 48
21. Kouidi E., Albani M., Natsis K., The effects of exercise training on muscle atrophy in haemodialysis patients Nephrology Dialysis Transplantation 1998 13 3 685 699
22. Binley K., Askham Z., Iqball S., Long-term reversal of chronic anemia using a hypoxia-regulated erythropoietin gene therapy Blood 2002 100 7 2406 2413
23. Maxwell P. H., Osmond M. K., Pugh C. W., Identification of the renal erythropoietin-producing cells using transgenic mice Kidney International 1993 44 5 1149 1162
24. Charifi N., Kadi F., Fasson L., Costes F., Geyssant A., Denis C., Enhancement of microvessel tortuosity in the vastus lateralis muscle of old men in response to endurance training Journal of Physiology 2004 554 2 559 569
25. Hepple R. T., A new measurement of tissue capillarity: the capillary-to-fibre perimeter exchange index Canadian Journal of Applied Physiology 1997 22 1 11 22
26. Jelkmann W., Erythropoietin Journal of Endocrinological Investigation 2003 26 9 832 837
27. Ameln H., Gustafsson T., Sundberg C. J., Physiological activation of hypoxia inducible factor-1 in human skeletal muscle FASEB Journal 2005 19 8 1009 1011
28. LeBaron M. J., Ahonen T. J., Nevalainen M. T., Rui H., In vivo response-based identification of direct hormone target cell populations using high-density tissue arrays Endocrinology 2007 148 3 989 1008
29. Rezaeian F., Wettstein R., Egger J.-F., Erythropoietin-induced upregulation of endothelial nitric oxide synthase but not vascular endothelial growth factor prevents musculocutaneous tissue from ischemic damage Laboratory Investigation 2010 90 1 40 51
30. Birot O., Bigard A. X., Rponses du rseau capillaire du muscle squelettique lentranement] Science and Sports 2003 18 1 1 10
31. Prior B. M., Lloyd P. G., Yang H. T., Terjung R. L., Exercise-induced vascular remodeling Exercise and Sport Sciences Reviews 2003 31 1 26 33
32. Hoppeler H., Vogt M., Muscle tissue adaptations to hypoxia The Journal of Experimental Biology 2001 204, part 18 3133 3139
33. Birot O. J., Exercise-induced expression of vascular endothelial growth factor mRNA in rat skeletal muscle is dependent on fibre type The Journal of Physiology 2003 552, part 1 213 221
34. Anagnostou A., Lee E. S., Kessimian N., Levinson R., Steiner M., Erythropoietin has a mitogenic and positive chemotactic effect on endothelial cells Proceedings of the National Academy of Sciences of the United States of America 1990 87 15 5978 5982
35. Richalet J. P., Herry J. P., Mdecine de Lalpinisme et des Sports de Montagne 2006 4th Paris, France Masson
36. Breen E., Tang K., Olfert M., Knapp A., Wagner P., Skeletal muscle capillarity during hypoxia: VEGF and its activation High Altitude Medicine and Biology 2008 9 2 158 166
37. Mathieu-Costello O., Muscle adaptation to altitude: tissue capillarity and capacity for aerobic metabolism High Altitude Medicine and Biology 2001 2 3 413 425
38. Hansen-Smith F. M., Blackwell L. H., Joswiak G. R., Expression of muscle capillary alkaline phosphatase is affected by hypoxia Journal of Applied Physiology 1992 73 2 776 780
39. Smith K., Marshall J. M., Physiological adjustments and arteriolar remodelling within skeletal muscle during acclimation to chronic hypoxia in the rat Journal of Physiology 1999 521 1 261 272
40. Snyder G. K., Wilcox E. E., Burnham E. W., Effects of hypoxia on muscle capillarity in rats Respiration Physiology 1985 62 1 135 140
41. Olfert I. M., Breen E. C., Mathieu-Costello O., Wagner P. D., Chronic hypoxia attenuates resting and exercise-induced VEGF, flt-1, and flk-1 mRNA levels in skeletal muscle Journal of Applied Physiology 2001 90 4 1532 1538
42. Deveci D., Marshall J. M., Egginton S., Relationship between capillary angiogenesis, fiber type, and fiber size in chronic systemic hypoxia American Journal of Physiology 2001 281 1 H241 H252
43. Armstrong R. B., Phelps R. O., Muscle fiber type composition of the rat hindlimb American Journal of Anatomy 1984 171 3 259 272
44. Luedeke J. D., McCall R. D., Dillaman R. M., Kinsey S. T., Properties of slow-and fast-twitch skeletal muscle from mice with an inherited capacity for hypoxic exercise Comparative Biochemistry and PhysiologyPart A 2004 138 3 373 382
45. Mattot V., Moons L., Lupu F., Loss of the VEGF164 and VEGF188 isoforms impairs postnatal glomerular angiogenesis and renal arteriogenesis in mice Journal of the American Society of Nephrology 2002 13 6 1548 1560
46. Zhang Y., Furumura M., Morita E., Distinct signaling pathways confer different vascular responses to VEGF 121 and VEGF 165 Growth Factors 2008 26 3 125 131
47. Kusters B., De Waal R. M. W., Wesseling P., Differential effects of vascular endothelial growth factor A isoforms in a mouse brain metastasis model of human melanoma Cancer Research 2003 63 17 5408 5413