Literature DB >> 35660921

Human induced pluripotent stem cells generated from Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome patients with a homozygous mutation in the PSMB8 gene (NIHTVBi016-A, NIHTVBi017-A, NIHTVBi018-A).

Quan Yu1, Atul Mehta1, Jizhong Zou2, Jeanette Beers2, Adriana A de Jesus Rasheed3, Raphaela Goldbach-Mansky3, Manfred Boehm1, Guibin Chen1.   

Abstract

We have successfully generated induced pluripotent stem cells (iPSC) from dermal fibroblasts and peripheral blood mononuclear cells from patients with a homozygous missense mutation in the gene encoding PSMB8. Biallelic loss of function mutations in this gene are responsible for the PSMB8 deficiency termed Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE). The iPSC carrying the homozygous PSMB8 gene mutation (c.224C > T, T75M) are phenotypically normal and have the capacity to differentiate toward the three germ layers. These iPSC have great potential to study the role of PMSB8 in the regulation of immune responses and other cellular pathways. Published by Elsevier B.V.

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Year:  2022        PMID: 35660921      PMCID: PMC9514390          DOI: 10.1016/j.scr.2022.102820

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   1.587


  5 in total

1.  Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.

Authors:  Yin Liu; Yuval Ramot; Antonio Torrelo; Amy S Paller; Nuo Si; Sofia Babay; Peter W Kim; Afzal Sheikh; Chyi-Chia Richard Lee; Yongqing Chen; Angel Vera; Xue Zhang; Raphaela Goldbach-Mansky; Abraham Zlotogorski
Journal:  Arthritis Rheum       Date:  2012-03

2.  Novel proteasome assembly chaperone mutations in PSMG2/PAC2 cause the autoinflammatory interferonopathy CANDLE/PRAAS4.

Authors:  Adriana A de Jesus; Anja Brehm; Rachel VanTries; Pascal Pillet; Anne-Sophie Parentelli; Gina A Montealegre Sanchez; Zuoming Deng; Isabelle Koné Paut; Raphaela Goldbach-Mansky; Elke Krüger
Journal:  J Allergy Clin Immunol       Date:  2019-01-18       Impact factor: 10.793

3.  Generation and characterization of a human iPSC line from a patient with propionic acidemia due to defects in the PCCA gene.

Authors:  Esmeralda Alonso-Barroso; Sandra Brasil; Álvaro Briso-Montiano; Rosa Navarrete; Celia Pérez-Cerdá; Magdalena Ugarte; Belén Pérez; Lourdes R Desviat; Eva Richard
Journal:  Stem Cell Res       Date:  2017-07-22       Impact factor: 2.020

4.  Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.

Authors:  Anja Brehm; Yin Liu; Afzal Sheikh; Bernadette Marrero; Ebun Omoyinmi; Qing Zhou; Gina Montealegre; Angelique Biancotto; Adam Reinhardt; Adriana Almeida de Jesus; Martin Pelletier; Wanxia L Tsai; Elaine F Remmers; Lela Kardava; Suvimol Hill; Hanna Kim; Helen J Lachmann; Andre Megarbane; Jae Jin Chae; Jilian Brady; Rhina D Castillo; Diane Brown; Angel Vera Casano; Ling Gao; Dawn Chapelle; Yan Huang; Deborah Stone; Yongqing Chen; Franziska Sotzny; Chyi-Chia Richard Lee; Daniel L Kastner; Antonio Torrelo; Abraham Zlotogorski; Susan Moir; Massimo Gadina; Phil McCoy; Robert Wesley; Kristina I Rother; Kristina Rother; Peter W Hildebrand; Paul Brogan; Elke Krüger; Ivona Aksentijevich; Raphaela Goldbach-Mansky
Journal:  J Clin Invest       Date:  2015-10-20       Impact factor: 14.808

5.  Generation of human induced pluripotent stem cells from individuals with a homozygous CCR5Δ32 mutation.

Authors:  Guibin Chen; Hui Jin; Zhen Yu; Yangtengyu Liu; Zhongwen Li; Keron Navarengom; Robin Schwartzbeck; Natalia Dmitrieva; Cornelia Cudrici; Elisa A Ferrante; Leslie G Biesecker; Dan Yang; Manfred Boehm
Journal:  Stem Cell Res       Date:  2019-06-05       Impact factor: 2.020

  5 in total

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