Normal and Pathological Red Cell Physiology

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre.  Allali S, Peyrard T, Amiranoff D, Cohen JF, Chalumeau M, Brousse V, de Montalembert M. Br J Haematol. 2017 Apr 12. doi:10.1111/bjh.14609.

Antioxidant and Membrane Binding Properties of Serotonin Protect Lipids from Oxidation. Azouzi S, Santuz H, Morandat S, Pereira C, Cote F, Hermine O, El Kirat K, Colin Y, Le Van Kim C, Etchebest C, Amireault P. Biophysical journal. 2017 May 09;112(9):1863-1873. doi:10.1016/j.bpj.2017.03.037

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation. Brusson M, Cochet S, Leduc M, Guillonneau F, Mayeux P, Peyrard T, Chomienne C, Le Van Kim C, Cassinat B, Kiladjian JJ, El Nemer W. Haematologica. 2017 Apr 06. doi:10.3324/haematol.2016.161604.

Cerebral and muscle microvascular oxygenation in children with sickle cell disease: Influence of hematology, hemorheology and vasomotion. Charlot K, Antoine-Jonville S, Moeckesch B, Jumet S, Romana M, Waltz X, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressieres B, Tarer V, Hue O, Etienne-Julan M, Connes P. Blood Cells Mol Dis. 2017 Apr 04;65:23-28. doi:10.1016/j.bcmd.2017.03.015.

Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia. Charlot K, Hierso R, Lemonne N, Romana M, Tressieres B, Lalanne-Mistrih ML, Etienne-Julan M, Tarer V, Ferracci S, Hardy-Dessources MD, Connes P. Br J Haematol. 2017 May;177(3):484-486. doi:10.1111/bjh.14064.

Effect of velaglucerase alfa enzyme replacement therapy on red blood cell properties in Gaucher disease. Franco M, Reihani N, Marin M, De Person M, Billette de Villemeur T, Rose C, Colin Y, Moussa F, Belmatoug N, Le Van Kim C. Am J Hematol. 2017 Jun 16. doi:10.1002/ajh.24816

Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients. Garnier Y, Ferdinand S, Etienne-Julan M, Elana G, Petras M, Doumdo L, Tressieres B, Lalanne-Mistrih ML, Hardy-Dessources MD, Connes P, Romana M. PloS one. 2017;12(5):e0177397. doi:10.1371/journal.pone.0177397.

Stomatin modulates the activity of the Anion Exchanger 1 (AE1, SLC4A1). Genetet S, Desrames A, Chouali Y, Ripoche P, Lopez C, Mouro-Chanteloup I. Sci Rep. 2017 Apr 07;7:46170. doi:10.1038/srep46170.

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles. Gourri E, Denomme GA, Merki Y, Scharberg EA, Vrignaud C, Frey BM, Peyrard T, Gassner C. Br J Haematol. 2017 Mar 08. doi:10.1111/bjh.14578.

Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study. Hierso R, Lemonne N, Villaescusa R, Lalanne-Mistrih ML, Charlot K, Etienne-Julan M, Tressieres B, Lamarre Y, Tarer V, Garnier Y, Hernandez AA, Ferracci S, Connes P, Romana M, Hardy-Dessources MD.. Br J Haematol. 2017 Mar;176(5):805-813. doi:10.1111/bjh.14476.

UGT1A1 (TA)n genotype is not the major risk factor of cholelithiasis in sickle cell disease children. Joly P, Renoux C, Lacan P, Bertrand Y, Cannas G, Garnier N, Cuzzubbo D, Kebaili K, Renard C, Gauthier A, Pialoux V, Martin C, Romana M, Connes P. Eur J Haematol. 2017 Mar;98(3):296-301. doi:10.1111/ejh.12838.

The endothelin B receptor plays a crucial role for the adhesion of neutrophils to the endothelium in sickle cell disease. Koehl B, Nivoit P, El Nemer W, Lenoir O, Hermand P, Pereira C, Brousse V, Guyonnet L, Ghinatti G, Benkerrou M, Colin Y, Le Van Kim C, Tharaux PL. Haematologica. 2017 Apr 06. doi:10.3324/haematol.2016.156869.

Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease.Mockesch B, Charlot K, Jumet S, Romana M, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressieres B, Tarer V, Hue O, Etienne-Julan M, Connes P, Antoine-Jonville S. Blood Cells Mol Dis. 2017 Feb 04;64:23-29. doi:10.1016/j.bcmd.2017.02.001.

Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease. Mockesch B, Connes P, Charlot K, Skinner S, Hardy-Dessources MD, Romana M, Jumet S, Petras M, Divialle-Doumdo L, Martin C, Tressieres B, Tarer V, Hue O, Etienne-Julan M, Antoine S, Pialoux V. Br J Haematol. 2017 May 03. doi:10.1111/bjh.14693.

Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon. Mombo LE, Mabioko-Mbembo G, Kassa-Kassa RF, Ontsitsagui E, Mboui-Ondo S, Nze-Kamsi L, Nkoghe D, Elion J. Hematology. 2017 Feb 23:1-6. doi:10.1080/10245332.2017.1292622

Intercalated Cell Depletion and Vacuolar H+-ATPase Mistargeting in an Ae1 R607H Knockin Model.Mumtaz R, Trepiccione F, Hennings JC, Huebner AK, Serbin B, Picard N, Ullah A, Paunescu TG, Capen DE, Lashhab RM, Mouro-Chanteloup I, Alper SL, Wagner CA, Cordat E, Brown D, Eladari D, Hubner CA. J Am Soc Nephrol. 2017 May;28(5):1507-1520. doi:10.1681/ASN.2016020169.

Joly P. Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes. Renoux C, Connes P, Nader E, Skinner S, Faes C, Petras M, Bertrand Y, Garnier N, Cuzzubbo D, Divialle-Doumdo L, Kebaili K, Renard C, Gauthier A, Etienne-Julan M, Cannas G, Martin C, Hardy-Dessources MD, Pialoux V, Romana M,. Pediatr Blood Cancer. 2017 Jan 18. doi:10.1002/pbc.26455. Cited in: Pubmed; PMID 28097791.

Gene Therapy in a Patient with Sickle Cell Disease. The New England journal of medicine. Ribeil JA, Hacein-Bey-Abina S, Payen E, Magnani A, Semeraro M, Magrin E, Caccavelli L, Neven B, Bourget P, El Nemer W, Bartolucci P, Weber L, Puy H, Meritet JF, Grevent D, Beuzard Y, Chretien S, Lefebvre T, Ross RW, Negre O, Veres G, Sandler L, Soni S, de Montalembert M, Blanche S, Leboulch P, Cavazzana M. 2017 Mar 02;376(9):848-855. doi:10.1056/NEJMoa1609677.

Spherocytic shift of red blood cells during storage provides a quantitative whole cell-based marker of the storage lesion Roussel C, Dussiot M, Marin M, Morel A, Ndour PA, Duez J, Le Van Kim C, Hermine O, Colin Y, Buffet P, Amireault P. Transfusion. 2017 Feb 01. doi:10.1111/trf.14015.

Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malaria. Tetard M, Milet J, Dechavanne S, Fievet N, Dorin-Semblat D, Elion J, Fairhurst RM, Deloron P, Tuikue-Ndam N, Gamain B. Sci Rep. 2017 May 03;7(1):1414. doi:10.1038/s41598-017-01495-9.

Recombinant Overexpression of Mammalian TSPO Isoforms 1 and 2. Senicourt L, Iatmanen-Harbi S, Hattab C, Ostuni MA, Giraud MF, Lacapere JJ. 2017 Meth Mol Biol 1635: 1-25.

Dynamic regulation of extracellular ATP in Escherichi coli. Alvarez CL, Corrradi G, Lauri N, Marginedas-Freixa I, Leal Denis MF, Enrique N, Mate SM, Milesi V, Ostuni MA, Herlax V, Schwarzbaum PJ. Biochemical Journal. 2017 Apr 15; 474(8): 1395-1416. DOI10.1042/BCJ20160879

 From Erythroblasts to Mature Red Blood Cells: Organelle Clearance in Mammals. Moras M, Lefevre SD, Ostuni MA. Front Physiol. 2017 Dec 19;8:1076. doi: 10.3389/fphys.2017.01076. eCollection 2017.