Kallikrein-related peptidases protein expression in lymphoid tissues suggests potential implications in immune response.


Journal

Clinical biochemistry
ISSN: 1873-2933
Titre abrégé: Clin Biochem
Pays: United States
ID NLM: 0133660

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 11 09 2019
revised: 02 12 2019
accepted: 27 12 2019
pubmed: 7 1 2020
medline: 3 4 2020
entrez: 7 1 2020
Statut: ppublish

Résumé

Kallikrein-related peptidases (KLKs) are a subgroup of 15 secreted chymotrypsin- and trypsin-like serine proteases that have been reported to possess novel functions in innate immunity and inflammation. Since the potential role of KLKs in immunity has not been studied in detail at the protein level, we examined the expression pattern of 12 members of the KLK family in immune-related tissues. Protein expression in tissue extracts was evaluated using immunoassays (ELISA). Immunohistochemistry (IHC) was performed on representative sections of tonsil and lymph nodes to determine the cellular localization of the KLK family members. ELISA profiling of KLK3-KLK15 (except KLK12) revealed higher protein levels in the tonsil, compared to the lymph nodes and spleen. Relatively high protein levels in the tonsil were observed for KLK7, KLK9, KLK10 and KLK13. Expression of these KLKs was significantly lower in lymph nodes and spleen. IHC analysis in tonsil unveiled that KLK9 and KLK10 were differentially expressed in lymphoid cells. KLK9 was strongly expressed in the germinal center of lymphoid follicles where activated B-cells reside, whereas KLK10 was expressed in the follicular dendritic cells (FDCs) that are vital for maintaining the cycle of B cell maturation. Overall, our study revealed the possible implications of KLK expression and regulation in the immune cells of lymphoid tissues.

Identifiants

pubmed: 31904348
pii: S0009-9120(19)31011-2
doi: 10.1016/j.clinbiochem.2019.12.015
pii:
doi:

Substances chimiques

RNA, Messenger 0
Peptide Hydrolases EC 3.4.-
Kallikreins EC 3.4.21.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-47

Informations de copyright

Copyright © 2020 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Panagiota S Filippou (PS)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada; Department of Clinical Biochemistry, University Health Network, Toronto, Canada.

Annie H Ren (AH)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada.

Antoninus Soosaipillai (A)

Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.

Roaa Safar (R)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada.

Ioannis Prassas (I)

Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.

Eleftherios P Diamandis (EP)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada; Department of Clinical Biochemistry, University Health Network, Toronto, Canada; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.

James R Conner (JR)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada. Electronic address: james.conner@sinaihealthsystem.ca.

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Classifications MeSH