A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease - Archive ouverte HAL
Article Dans Une Revue Science Advances Année : 2024

A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease

Anne Molitor (1, 2, 3, 4, 5, 6) , Alexandre Lederle (1, 2, 7, 5, 3, 4, 6) , Mirjana Radosavljevic (1, 2, 5, 3, 4, 6, 8, 9) , Vinay Sapuru (10, 11) , Megan Zavorka Thomas (12) , Jianying Yang (1, 2, 5, 3, 4, 6) , Mahsa Shirin (1, 2, 5, 3, 4, 6) , Virginie Collin-Bund (1, 2, 5, 3, 4, 6) , Katerina Jerabkova-Roda (5, 1, 7, 2, 3, 4) , Zhichao Miao (13, 14) , Alice Bernard (5, 1, 2, 3, 4, 6, 8, 9) , Véronique Rolli (5, 1, 2, 3, 4, 6, 8, 9) , Pierre Grenot (5, 1, 2, 3, 4, 6, 8, 9) , Carla Noemi Castro (15) , Michelle Rosenzwajg (16, 17, 18) , Elyssa Lewis (19) , Richard Person (20) , Uxía-Saraiva Esperón-Moldes (21) , Milja Kaare (21) , Pekka Nokelainen (21) , Nurit Assia Batzir (22) , Gal Zaks Hoffer (22) , Nicodème Paul (5, 1, 2, 3, 4, 6) , Tristan Stemmelen (5, 1, 2, 3, 4, 6, 8, 9) , Lydie Naegely (5, 1, 2, 3, 4, 6) , Antoine Hanauer (5, 1, 2, 3, 4, 6) , Sabrina Bibi-Triki (5, 1, 2, 3, 4, 6) , Sarah Grün (15) , Sophie Jung (5, 1, 2, 3, 4, 9) , Ignacio Busnelli (5, 1, 2, 3, 4) , Kornelia Tripolszki (23) , Ruslan Al-Ali (23) , Natalia Ordonez (23) , Peter Bauer (23) , Eunkyung Song (12) , Kristin Zajo (12) , Santiago Partida-Sanchez (12) , Frank Robledo-Avila (12) , Attila Kumanovics (24) , Yoram Louzoun (25) , Aurélie Hirschler (26, 27, 28) , Angélique Pichot (5, 1, 2, 3, 4, 6) , Ori Toker (29, 30) , Cesar Andrés Muñoz Mejía , Nima Parvaneh (31) , Esther Knapp (19) , Joseph Hersh (19) , Heather Kenney (32) , Ottavia Delmonte (32) , Luigi Notarangelo (32) , Jacky Goetz (5, 1, 2, 3, 4) , Samir Kahwash (12) , Christine Carapito (28, 27, 26) , Rajinder Bajwa (12) , Caroline Thomas (33) , Stephan Ehl (15) , Bertrand Isidor (34) , Raphael Carapito (5, 1, 2, 3, 4, 6, 9, 8) , Roshini Abraham (12) , Richard Hite (10) , Nufar Marcus (22, 35, 36) , Aida Bertoli-Avella (23) , Seiamak Bahram (5, 1, 2, 3, 4, 6, 9, 8)
1 IRM - Immuno-Rhumatologie Moléculaire
2 GENOMAX [plateforme]
3 Centre de Recherche d’Immunologie et d’Hématologie [Strasbourg]
4 CRBS - Centre de Recherche en Biomédecine de Strasbourg
5 FMTS - Fédération de Médecine Translationnelle de Strasbourg
6 Laboratoire d'excellence (Labex) Transplantex (Nouveaux loci d’histocompatibilité et biomarqueurs en transplantation humaine, de la découverte à l’application clinique)
7 UNISTRA - Université de Strasbourg
8 Nouvel Hôpital Civil de Strasbourg
9 HUS - Les Hôpitaux Universitaires de Strasbourg
10 MSK2C - Memorial Sloan Kettering Cancer Center [New York, NY, USA]
11 Weill Cornell Medicine [Cornell University]
12 Nationwide Children's Hospital
13 GIBI - Guangzhou International Bio Island [Guangdong, China]
14 Tongji University School of Medicine [Shanghai, China]
15 Albert-Ludwigs-Universität Freiburg = University of Freiburg
16 I3 - Immunologie - Immunopathologie - Immunothérapie [CHU Pitié Salpêtrière]
17 CIC-BTi - Centre d'investigation clinique Biothérapie [CHU Pitié-Salpêtrière]
18 CHU Pitié-Salpêtrière [AP-HP]
19 University of Louisville School of Medicine [Louisville]
20 GeneDx [Gaithersburg, MD, USA]
21 Blueprint Genetics
22 Schneider Children’s Medical Center of Israel [Petah Tikva]
23 CENTOGENE AG
24 Mayo Clinic [Rochester]
25 Bar-Ilan University [Israël]
26 IPHC - Institut Pluridisciplinaire Hubert Curien
27 LSMBO - Laboratoire de Spectrométrie de Masse BioOrganique [Strasbourg]
28 FR ProFI - Fédération de Recherche nationale ProFI
29 Shaare Zedek Medical Center [Jerusalem, Israel]
30 HUJ - The Hebrew University of Jerusalem
31 IUMS - Iran University of Medical Sciences [Tehran, Iran]
32 NIAID-NIH - National Institute of Allergy and Infectious Diseases [Bethesda]
33 CHU Nantes - Centre Hospitalier Universitaire de Nantes = Nantes University Hospital
34 Hôtel-Dieu de Nantes
35 TAU - Tel Aviv University
36 Jeffrey Modell Foundation
Megan Zavorka Thomas
Richard Person
Milja Kaare
  • Fonction : Auteur
Kornelia Tripolszki
  • Fonction : Auteur
Ruslan Al-Ali
  • Fonction : Auteur
Natalia Ordonez
  • Fonction : Auteur
Peter Bauer
Kristin Zajo
Santiago Partida-Sanchez
Frank Robledo-Avila
Attila Kumanovics
Yoram Louzoun
Cesar Andrés Muñoz Mejía
Samir Kahwash
Rajinder Bajwa
Bertrand Isidor
Roshini Abraham
Aida Bertoli-Avella
  • Fonction : Auteur

Résumé

Inositol 1,4,5-trisphosphate (IP3) receptor type 1 ( ITPR1 ), 2 ( ITPR2 ), and 3 ( ITPR3 ) encode the IP3 receptor (IP3R), a key player in intracellular calcium release. In four unrelated patients, we report that an identical ITPR3 de novo variant—NM_002224.3:c.7570C>T, p.Arg2524Cys—causes, through a dominant-negative effect, a complex multisystemic disorder with immunodeficiency. This leads to defective calcium homeostasis, mitochondrial malfunction, CD4 + lymphopenia, a quasi-absence of naïve CD4 + and CD8 + cells, an increase in memory cells, and a distinct TCR repertoire. The calcium defect was recapitulated in Jurkat knock-in. Site-directed mutagenesis displayed the exquisite sensitivity of Arg 2524 to any amino acid change. Despite the fact that all patients had severe immunodeficiency, they also displayed variable multisystemic involvements, including ectodermal dysplasia, Charcot-Marie-Tooth disease, short stature, and bone marrow failure. In conclusion, unlike previously reported ITPR1-3 deficiencies leading to narrow, mainly neurological phenotypes, a recurrent dominant ITPR3 variant leads to a multisystemic disease, defining a unique role for IP3R3 in the tetrameric IP3R complex.
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Dates et versions

hal-04752335 , version 1 (24-10-2024)

Identifiants

Citer

Anne Molitor, Alexandre Lederle, Mirjana Radosavljevic, Vinay Sapuru, Megan Zavorka Thomas, et al.. A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease. Science Advances , 2024, 10 (37), pp.eado5545. ⟨10.1126/sciadv.ado5545⟩. ⟨hal-04752335⟩
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