» Articles » PMID: 30251416

Lymphocytes Are a Major Source of Circulating Soluble Dipeptidyl Peptidase 4

Overview
Date 2018 Sep 26
PMID 30251416
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Dipeptidyl peptidase 4 (DPP4, CD26) is a serine protease that is expressed constitutively by many haematopoietic and non-haematopoietic tissues. It exists as a membrane-associated protein, as well as in an active, soluble form (herein called sDPP4), present at high concentrations in bodily fluids. Despite the proposed use of sDPP4 as a biomarker for multiple diseases, its cellular sources are not well defined. Here, we report that individuals with congenital lymphocyte immunodeficiency had markedly lower serum concentrations of sDPP4, which were restored upon successful treatment and restoration of lymphocyte haematopoiesis. Using irradiated lymphopenic mice and wild-type to Dpp4 reciprocal bone marrow chimeric animals, we found that haematopoietic cells were a major source of circulating sDPP4. Furthermore, activation of human and mouse T lymphocytes resulted in increased sDPP4, providing a mechanistic link between immune system activation and sDPP4 concentration. Finally, we observed that acute viral infection induced a transient increase in sDPP4, which correlated with the expansion of antigen-specific CD8 T cell responses. Our study demonstrates that sDPP4 concentrations are determined by the frequency and activation state of lymphocyte populations. Insights from these studies will support the use of sDPP4 concentration as a biomarker for inflammatory and infectious diseases.

Citing Articles

Transport functions of intestinal lymphatic vessels.

Tso P, Bernier-Latmani J, Petrova T, Liu M Nat Rev Gastroenterol Hepatol. 2024; 22(2):127-145.

PMID: 39496888 DOI: 10.1038/s41575-024-00996-z.


Exploring the conformational dynamics and key amino acids in the CD26-caveolin-1 interaction and potential therapeutic interventions.

Hu X, Jiang C, Gu Y, Xue X Medicine (Baltimore). 2024; 103(22):e38367.

PMID: 39259075 PMC: 11142805. DOI: 10.1097/MD.0000000000038367.


Soluble CD26: From Suggested Biomarker for Cancer Diagnosis to Plausible Marker for Dynamic Monitoring of Immunotherapy.

Kotrulev M, Gomez-Tourino I, Cordero O Cancers (Basel). 2024; 16(13).

PMID: 39001488 PMC: 11240764. DOI: 10.3390/cancers16132427.


A Systems Biology Approach Unveils a Critical Role of DPP4 in Upper Gastrointestinal Cancer Patient Outcomes.

Kotnala S, Dhasmana A, Dhasmana S, Haque S, Yallapu M, Tripathi M J Environ Pathol Toxicol Oncol. 2024; 43(2):43-55.

PMID: 38505912 PMC: 11419273. DOI: 10.1615/JEnvironPatholToxicolOncol.2023048056.


StructuralDPPIV: a novel deep learning model based on atom structure for predicting dipeptidyl peptidase-IV inhibitory peptides.

Wang D, Jin J, Li Z, Wang Y, Fan M, Liang S Bioinformatics. 2024; 40(2).

PMID: 38305458 PMC: 10904144. DOI: 10.1093/bioinformatics/btae057.


References
1.
Gorrell M, Gysbers V, McCaughan G . CD26: a multifunctional integral membrane and secreted protein of activated lymphocytes. Scand J Immunol. 2001; 54(3):249-64. DOI: 10.1046/j.1365-3083.2001.00984.x. View

2.
Tanaka T, Duke-Cohan J, Kameoka J, YARON A, Lee I, Schlossman S . Enhancement of antigen-induced T-cell proliferation by soluble CD26/dipeptidyl peptidase IV. Proc Natl Acad Sci U S A. 1994; 91(8):3082-6. PMC: 43519. DOI: 10.1073/pnas.91.8.3082. View

3.
Decalf J, Tarbell K, Casrouge A, Price J, Linder G, Mottez E . Inhibition of DPP4 activity in humans establishes its in vivo role in CXCL10 post-translational modification: prospective placebo-controlled clinical studies. EMBO Mol Med. 2016; 8(6):679-83. PMC: 4888857. DOI: 10.15252/emmm.201506145. View

4.
Klemann C, Wagner L, Stephan M, von Horsten S . Cut to the chase: a review of CD26/dipeptidyl peptidase-4's (DPP4) entanglement in the immune system. Clin Exp Immunol. 2016; 185(1):1-21. PMC: 4908298. DOI: 10.1111/cei.12781. View

5.
Barreira da Silva R, Laird M, Yatim N, Fiette L, Ingersoll M, Albert M . Dipeptidylpeptidase 4 inhibition enhances lymphocyte trafficking, improving both naturally occurring tumor immunity and immunotherapy. Nat Immunol. 2015; 16(8):850-8. DOI: 10.1038/ni.3201. View