Splenectomy improves erythrocyte functionality in spherocytosis based on septin abundance, but not maturation defects.
Journal
Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425
Informations de publication
Date de publication:
12 09 2023
12 09 2023
Historique:
accepted:
13
01
2023
received:
11
10
2022
medline:
24
8
2023
pubmed:
9
2
2023
entrez:
8
2
2023
Statut:
ppublish
Résumé
Splenectomy improves the clinical parameters of patients with hereditary spherocytosis, but its potential benefit to red blood cell (RBC) functionality and the mechanism behind this benefit remain largely overlooked. Here, we compared 7 nonsplenectomized and 13 splenectomized patients with mutations in the β-spectrin or the ankyrin gene. We showed that hematological parameters, spherocyte abundance, osmotic fragility, intracellular calcium, and extracellular vesicle release were largely but not completely restored by splenectomy, whereas cryohemolysis was not. Affected RBCs exhibited decreases in β-spectrin and/or ankyrin contents and slight alterations in spectrin membrane distribution, depending on the mutation. These modifications were found in both splenectomized and nonsplenectomized patients and poorly correlated with RBC functionality alteration, suggesting additional impairments. Accordingly, we found an increased abundance of septins, small guanosine triphosphate-binding cytoskeletal proteins. Septins-2, -7, and -8 but not -11 were less abundant upon splenectomy and correlated with the disease severity. Septin-2 membrane association was confirmed by immunolabeling. Except for cryohemolysis, all parameters of RBC morphology and functionality correlated with septin abundance. The increased septin content might result from RBC maturation defects, as evidenced by (1) the decreased protein 4.2 and Rh-associated glycoprotein content in all patient RBCs, (2) increased endoplasmic reticulum remnants and endocytosis proteins in nonsplenectomized patients, and (3) increased lysosomal and mitochondrial remnants in splenectomized patients. Our study paves the way for a better understanding of the involvement of septins in RBC membrane biophysical properties. In addition, the lack of restoration of septin-independent cryohemolysis by splenectomy may call into question its recommendation in specific cases.
Identifiants
pubmed: 36753606
pii: 494357
doi: 10.1182/bloodadvances.2022009114
pmc: PMC10468371
doi:
Substances chimiques
Spectrin
12634-43-4
Septins
EC 3.6.1.-
Ankyrins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
4705-4720Informations de copyright
© 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
Références
Front Physiol. 2019 Apr 16;10:386
pubmed: 31040790
Haematologica. 2014 Feb;99(2):267-75
pubmed: 23975182
Blood. 1973 Jul;42(1):1-8
pubmed: 4717407
J Cell Sci. 2018 Jan 11;131(1):
pubmed: 29326311
Cell Physiol Biochem. 2018;51(4):1544-1565
pubmed: 30497064
Front Physiol. 2017 Sep 06;8:673
pubmed: 28932200
Expert Rev Hematol. 2011 Dec;4(6):627-35
pubmed: 22077527
Phys Biol. 2008 Aug 13;5(3):036007
pubmed: 18698116
Proc Natl Acad Sci U S A. 2018 Sep 18;115(38):9574-9579
pubmed: 30190436
Curr Health Sci J. 2016 Oct-Dec;42(4):408-412
pubmed: 30581596
Front Cell Dev Biol. 2021 Nov 11;9:768409
pubmed: 34858990
Haematologica. 2016 Sep;101(9):1018-27
pubmed: 27247322
Blood. 2002 Sep 15;100(6):2208-15
pubmed: 12200387
Nanoscale Horiz. 2018 May 1;3(3):293-304
pubmed: 32254077
Front Cell Dev Biol. 2016 Nov 03;4:124
pubmed: 27857942
Clin Chim Acta. 1984 Sep 29;142(2):183-92
pubmed: 6499204
Nouv Rev Fr Hematol. 1972 Nov-Dec;12(6):721-45
pubmed: 4268780
Ann Intern Med. 1967 Nov;67(5):990-7
pubmed: 6050825
Blood. 2012 Jun 21;119(25):6118-27
pubmed: 22461493
Blood Rev. 2013 Jul;27(4):167-78
pubmed: 23664421
Front Physiol. 2018 Jun 01;9:656
pubmed: 29910743
Pediatr Surg Int. 2020 Mar;36(3):365-371
pubmed: 31982941
Blood. 2016 Mar 24;127(12):1616-8
pubmed: 26773041
Br J Haematol. 2022 Aug;198(3):574-586
pubmed: 35670632
Front Physiol. 2017 Dec 19;8:1076
pubmed: 29311991
Front Physiol. 2020 Jul 03;11:712
pubmed: 32719614
Br J Haematol. 1994 Sep;88(1):52-5
pubmed: 7803256
Am J Hematol. 1998 Jul;58(3):206-12
pubmed: 9662272
Haematologica. 2016 Nov;101(11):1284-1294
pubmed: 27756835
Proc Natl Acad Sci U S A. 2009 Sep 8;106(36):15320-5
pubmed: 19717437
Front Physiol. 2021 Feb 23;12:638027
pubmed: 33708142
iScience. 2022 Jun 22;25(7):104654
pubmed: 35832887
Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1289-94
pubmed: 20080583
Int J Mol Sci. 2013 May 08;14(5):9848-72
pubmed: 23698771
Haematologica. 2017 Aug;102(8):1304-1313
pubmed: 28550188
Br J Haematol. 2008 May;141(3):367-75
pubmed: 18341630
J Clin Invest. 1965 Aug;44:1417-24
pubmed: 14322046
Lancet. 2008 Oct 18;372(9647):1411-26
pubmed: 18940465
Nat Rev Immunol. 2005 Aug;5(8):606-16
pubmed: 16056254
Cytoskeleton (Hoboken). 2019 Jan;76(1):143-153
pubmed: 30019536
Am J Hematol. 1984 Aug;17(2):129-39
pubmed: 6465132
Biomolecules. 2020 Jul 29;10(8):
pubmed: 32751168
Int J Mol Sci. 2020 Nov 28;21(23):
pubmed: 33260618
Acta Haematol. 2018;139(1):60-66
pubmed: 29402830
Front Physiol. 2021 Mar 25;12:641384
pubmed: 33841180
Pediatrics. 2015 Jun;135(6):1107-14
pubmed: 26009624
Blood. 2010 Jul 15;116(2):267-9
pubmed: 20339087
Protoplasma. 2010 Aug;244(1-4):99-131
pubmed: 20668894
Pediatr Res. 1975 Dec;9(12):928-31
pubmed: 127974
Exp Hematol. 2020 Sep;89:43-54.e2
pubmed: 32750404
Nat Commun. 2019 Jan 24;10(1):420
pubmed: 30679428
Front Immunol. 2017 Feb 02;8:73
pubmed: 28210260
Cell Biochem Biophys. 2016 Sep;74(3):365-71
pubmed: 27557951
Haematologica. 2020 Jan 31;105(2):338-347
pubmed: 31147440
Nano Lett. 2021 Jun 23;21(12):4950-4958
pubmed: 34125553