Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses

Ole E. Sørensen; Stine N Clemmensen; Sara L Dahl; Ole Østergaard; Niels H H Heegaard; Andreas Glenthøj; Finn Cilius Nielsen; Niels Borregaard

doi:10.1172/JCI76009

Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses

Ole E. Sørensen, Stine N Clemmensen, Sara L Dahl, Ole Østergaard, Niels H H Heegaard, Andreas Glenthøj, Finn Cilius Nielsen, Niels Borregaard

Department of Clinical Medicine

104 Citations (Scopus)

Abstract

Papillon-Lefèvre syndrome (PLS) results from mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine proteases considered essential for antimicrobial defense. Despite serine protease-deficient immune cell populations, PLS patients do not exhibit marked immunodeficiency. Here, we characterized a 24-year-old woman who had suffered from severe juvenile periodontal disease, but was otherwise healthy, and identified a homozygous missense mutation in CTSC indicative of PLS. Proteome analysis of patient neutrophil granules revealed that several proteins that normally localize to azurophil granules, including the major serine proteases, elastase, cathepsin G, and proteinase 3, were absent. Accordingly, neutrophils from this patient were incapable of producing neutrophil extracellular traps (NETs) in response to ROS and were unable to process endogenous cathelicidin hCAP-18 into the antibacterial peptide LL-37 in response to ionomycin. In immature myeloid cells from patient bone marrow, biosynthesis of CTSC and neutrophil serine proteases appeared normal along with initial processing and sorting to cellular storage. In contrast, these proteins were completely absent in mature neutrophils, indicating that CTSC mutation promotes protease degradation in more mature hematopoietic subsets, but does not afect protease production in progenitor cells. Together, these data indicate CTSC protects serine proteases from degradation in mature immune cells and suggest that neutrophil serine proteases are dispensable for human immunoprotection.

Original language	English
Journal	The Journal of Clinical Investigation
Volume	124
Issue number	10
Pages (from-to)	4539-48
Number of pages	10
ISSN	0021-9738
DOIs	https://doi.org/10.1172/JCI76009
Publication status	Published - 1 Oct 2014

Keywords

Adult
Antimicrobial Cationic Peptides
Bone Marrow
Cathepsin C
Cell Separation
Defensins
Female
Flow Cytometry
Homozygote
Humans
Immune System
Ionomycin
Mutation, Missense
Neutrophils
Papillon-Lefevre Disease
Proteome
Reactive Oxygen Species
Serine Proteases
Subcellular Fractions

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1172/JCI76009

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title = "Papillon-Lef{\`e}vre syndrome patient reveals species-dependent requirements for neutrophil defenses",

abstract = "Papillon-Lef{\`e}vre syndrome (PLS) results from mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine proteases considered essential for antimicrobial defense. Despite serine protease-deficient immune cell populations, PLS patients do not exhibit marked immunodeficiency. Here, we characterized a 24-year-old woman who had suffered from severe juvenile periodontal disease, but was otherwise healthy, and identified a homozygous missense mutation in CTSC indicative of PLS. Proteome analysis of patient neutrophil granules revealed that several proteins that normally localize to azurophil granules, including the major serine proteases, elastase, cathepsin G, and proteinase 3, were absent. Accordingly, neutrophils from this patient were incapable of producing neutrophil extracellular traps (NETs) in response to ROS and were unable to process endogenous cathelicidin hCAP-18 into the antibacterial peptide LL-37 in response to ionomycin. In immature myeloid cells from patient bone marrow, biosynthesis of CTSC and neutrophil serine proteases appeared normal along with initial processing and sorting to cellular storage. In contrast, these proteins were completely absent in mature neutrophils, indicating that CTSC mutation promotes protease degradation in more mature hematopoietic subsets, but does not afect protease production in progenitor cells. Together, these data indicate CTSC protects serine proteases from degradation in mature immune cells and suggest that neutrophil serine proteases are dispensable for human immunoprotection.",

keywords = "Adult, Antimicrobial Cationic Peptides, Bone Marrow, Cathepsin C, Cell Separation, Defensins, Female, Flow Cytometry, Homozygote, Humans, Immune System, Ionomycin, Mutation, Missense, Neutrophils, Papillon-Lefevre Disease, Proteome, Reactive Oxygen Species, Serine Proteases, Subcellular Fractions",

author = "S{\o}rensen, {Ole E.} and Clemmensen, {Stine N} and Dahl, {Sara L} and Ole {\O}stergaard and Heegaard, {Niels H H} and Andreas Glenth{\o}j and Nielsen, {Finn Cilius} and Niels Borregaard",

year = "2014",

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doi = "10.1172/JCI76009",

language = "English",

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journal = "Journal of Clinical Investigation",

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T1 - Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses

AU - Sørensen, Ole E.

AU - Clemmensen, Stine N

AU - Dahl, Sara L

AU - Østergaard, Ole

AU - Heegaard, Niels H H

AU - Glenthøj, Andreas

AU - Nielsen, Finn Cilius

AU - Borregaard, Niels

PY - 2014/10/1

Y1 - 2014/10/1

N2 - Papillon-Lefèvre syndrome (PLS) results from mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine proteases considered essential for antimicrobial defense. Despite serine protease-deficient immune cell populations, PLS patients do not exhibit marked immunodeficiency. Here, we characterized a 24-year-old woman who had suffered from severe juvenile periodontal disease, but was otherwise healthy, and identified a homozygous missense mutation in CTSC indicative of PLS. Proteome analysis of patient neutrophil granules revealed that several proteins that normally localize to azurophil granules, including the major serine proteases, elastase, cathepsin G, and proteinase 3, were absent. Accordingly, neutrophils from this patient were incapable of producing neutrophil extracellular traps (NETs) in response to ROS and were unable to process endogenous cathelicidin hCAP-18 into the antibacterial peptide LL-37 in response to ionomycin. In immature myeloid cells from patient bone marrow, biosynthesis of CTSC and neutrophil serine proteases appeared normal along with initial processing and sorting to cellular storage. In contrast, these proteins were completely absent in mature neutrophils, indicating that CTSC mutation promotes protease degradation in more mature hematopoietic subsets, but does not afect protease production in progenitor cells. Together, these data indicate CTSC protects serine proteases from degradation in mature immune cells and suggest that neutrophil serine proteases are dispensable for human immunoprotection.

AB - Papillon-Lefèvre syndrome (PLS) results from mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine proteases considered essential for antimicrobial defense. Despite serine protease-deficient immune cell populations, PLS patients do not exhibit marked immunodeficiency. Here, we characterized a 24-year-old woman who had suffered from severe juvenile periodontal disease, but was otherwise healthy, and identified a homozygous missense mutation in CTSC indicative of PLS. Proteome analysis of patient neutrophil granules revealed that several proteins that normally localize to azurophil granules, including the major serine proteases, elastase, cathepsin G, and proteinase 3, were absent. Accordingly, neutrophils from this patient were incapable of producing neutrophil extracellular traps (NETs) in response to ROS and were unable to process endogenous cathelicidin hCAP-18 into the antibacterial peptide LL-37 in response to ionomycin. In immature myeloid cells from patient bone marrow, biosynthesis of CTSC and neutrophil serine proteases appeared normal along with initial processing and sorting to cellular storage. In contrast, these proteins were completely absent in mature neutrophils, indicating that CTSC mutation promotes protease degradation in more mature hematopoietic subsets, but does not afect protease production in progenitor cells. Together, these data indicate CTSC protects serine proteases from degradation in mature immune cells and suggest that neutrophil serine proteases are dispensable for human immunoprotection.

KW - Adult

KW - Antimicrobial Cationic Peptides

KW - Bone Marrow

KW - Cathepsin C

KW - Cell Separation

KW - Defensins

KW - Female

KW - Flow Cytometry

KW - Homozygote

KW - Humans

KW - Immune System

KW - Ionomycin

KW - Mutation, Missense

KW - Neutrophils

KW - Papillon-Lefevre Disease

KW - Proteome

KW - Reactive Oxygen Species

KW - Serine Proteases

KW - Subcellular Fractions

U2 - 10.1172/JCI76009

DO - 10.1172/JCI76009

M3 - Journal article

C2 - 25244098

SN - 0021-9738

VL - 124

SP - 4539

EP - 4548

JO - Journal of Clinical Investigation

JF - Journal of Clinical Investigation

IS - 10

ER -

Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses

Abstract

Keywords

UN SDGs

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