| Literature DB >> 35660921 |
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.Entities:
Mesh:
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