Divergent Pathways of Surfactant Protein C Maturation for Disease-Associated Isoforms

ABSTRACT Surfactant Protein C (SP-C), a hydrophobic protein exclusively synthesized and secreted by alveolar type II (AT2) cells, is important for reducing alveolar surface tension in the distal lung. Chronic interstitial pulmonary diseases have been associated with SFTPC mutations. However, a detailed understanding of SP-C maturation in the secretory pathway and disruptions caused by mutations has remained incomplete. The goal of this study was to comprehensively ascertain differences in trafficking and post-translational processing between wild-type and disease-associated SP-C mutants using doxycycline-inducible mouse lung epithelial (MLE-12) cell lines expressing either wildtype SP-C or the common clinical variant SP-CI73T, validated using primary AT2 cells isolated from a murine SP-CI73T pulmonary fibrosis model and induced pluripotent stem cell (iPSC)-derived human alveolar type 2 cells (iAT2s) expressing the same mutant. In all 3 models SP-CWT was highly concentrated in acidic LROs while SP-CI73T accumulated on the plasma membrane, which was corroborated by inhibition of clathrin-mediated endocytosis, surface biotinylation, immunogold EM, immunofluorescent staining in non-permeabilized cells, and proteinase K protection assays supporting divergence of SP-CI73T trafficking from SP-CWT. The exclusion of SP-CI73T from normal routing occurred early in the biosynthetic pathway as Brefeldin A blocked processing of both SP-C proproteins, while a 20°C temperature shift caused selective accumulation of a processed proSP-CWT intermediate, suggesting initial C-terminal cleavage of proSP-CWT occurs in late-Golgi/ trans-Golgi network (TGN). This cleavage event was sensitive to DC1, an inhibitor of furin-related subtilisin-like proprotein convertase (PPC) family members. Site-directed mutagenesis of canonical residues K160, R167 within a predicted PPC recognition site in the proSP-C BRICHOS domain blocked its processing. Expression constructs encoding inhibitory pre-proprotein (pp) peptide fragments of Furin and ppPC7 each inhibited cleavage of proSP-CWT by MLE-12 cells. Collectively, our data demonstrate that trafficking pathways for maturation of WT and mutant I73T SP-C diverge prior to the TGN where initial cleavage of the COOH-terminal SP-C propeptide occurs via a Furin-like proprotein convertase. Competing Interest Statement The authors have declared no competing interest. Footnotes Funding: NIH 1R01HL145408 (MFB), VA Merit Review 2I01 BX001176(MFB), NIH U01 HL119436 (MFB), the Perelman School of Medicine Dyson IPF Accelerator Fund (MFB), NIH F32 HL160011 (LRR), Pulmonary Fibrosis Foundation Scholar Award (LRR), NIH K99 HL171946 (LRR), NIH K08 HL163494 (KDA), a Boston University School of Medicine Department of Medicine Career Investment Award (KDA), NIH U01 HL134745 (DNK), NIH U01 HL134766 (DNK), NIH U01 HL152976 (DNK), NIH R01 HL095993 (DNK), U01HL148692 (DNK), NIH P01 HL170952 (KDA, DNK), and NIH N01 75N92025R00004 (DNK), NIH U01148856 (JAW), U01HL134745 (JAW), U01HL136722 (JAW), and U01HL148860 (JAW). Conflict of Interest: The authors declare that no conflicts of interest exist.