Details

Autor(en) / Beteiligte

• Preisendörfer, Stefan
• Ishikawa, Yoshihiro
• Hennen, Elisabeth
• Winklmeier, Stephan
• Schupp, Jonas C
• Knüppel, Larissa
• Fernandez, Isis E
• Binzenhöfer, Leonhard
• Flatley, Andrew
• Juan-Guardela, Brenda M
• Ruppert, Clemens
• Guenther, Andreas
• Frankenberger, Marion
• Hatz, Rudolf A
• Kneidinger, Nikolaus
• Behr, Jürgen
• Feederle, Regina
• Schepers, Aloys
• Hilgendorff, Anne
• Kaminski, Naftali
• Meinl, Edgar
• Bächinger, Hans Peter
• Eickelberg, Oliver
• Staab-Weijnitz, Claudia A

Titel

FK506-Binding Protein 11 Is a Novel Plasma Cell-Specific Antibody Folding Catalyst with Increased Expression in Idiopathic Pulmonary Fibrosis

Ist Teil von

• Cells (Basel, Switzerland), 2022-04, Vol.11 (8), p.1341

Ort / Verlag

Switzerland: MDPI AG

Erscheinungsjahr

2022

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Antibodies are central effectors of the adaptive immune response, widespread used therapeutics, but also potentially disease-causing biomolecules. Antibody folding catalysts in the plasma cell are incompletely defined. Idiopathic pulmonary fibrosis (IPF) is a fatal chronic lung disease with increasingly recognized autoimmune features. We found elevated expression of FK506-binding protein 11 ( ) in IPF lungs where FKBP11 specifically localized to antibody-producing plasma cells. Suggesting a general role in plasma cells, plasma cell-specific expression was equally observed in lymphatic tissues, and in vitro B cell to plasma cell differentiation was accompanied by induction of expression. Recombinant human FKBP11 was able to refold IgG antibody in vitro and inhibited by FK506, strongly supporting a function as antibody peptidyl-prolyl isomerase. Induction of ER stress in cell lines demonstrated induction of in the context of the unfolded protein response in an X-box-binding protein 1 (XBP1)-dependent manner. While deficiency of FKBP11 increased susceptibility to ER stress-mediated cell death in an alveolar epithelial cell line, FKBP11 knockdown in an antibody-producing hybridoma cell line neither induced cell death nor decreased expression or secretion of IgG antibody. Similarly, antibody secretion by the same hybridoma cell line was not affected by knockdown of the established antibody peptidyl-prolyl isomerase cyclophilin B. The results are consistent with FKBP11 as a novel XBP1-regulated antibody peptidyl-prolyl isomerase and indicate significant redundancy in the ER-resident folding machinery of antibody-producing hybridoma cells.