Literature DB >> 33811483

Platelet and neutrophil responses to Porphyromonas gingivalis in human whole blood.

William A Chen1, Hansel M Fletcher2, Kimberly J Payne3, Sheryl Aka4, Melanie B Thornburg4, Joseph D Gheorghe4, Shahnaj Binte Safi5, David Shavlik5, Udochukwu Oyoyo6, Danilo S Boskovic1.   

Abstract

Porphyromonas gingivalis is a causative agent for periodontal disease. Binding of platelets to this gram-negative anaerobe can regulate host hemostatic (thrombus forming) and immune (neutrophil interacting) responses during bacterial infection. Additionally, in response to bacterial pathogens neutrophils can release their DNA, forming highly prothrombotic neutrophil extracellular traps (NETs), which then further enhance platelet responses. This study evaluates the role of P. gingivalis on platelet expression of CD62P, platelet-neutrophil interactions, and labeled neutrophil-associated DNA. Human whole blood was preincubated with varying P. gingivalis concentrations, with or without subsequent addition of adenosine diphosphate (ADP). Flow cytometry was employed to measure platelet expression of CD62P using PerCP-anti-CD61 and PE-anti-CD62P, platelet-neutrophil interactions using PerCP-anti-CD61 and FITC-anti-CD16, and the release of neutrophil DNA using FITC-anti-CD16 and Sytox Blue labeling. Preincubation with a high (6.25 × 106  CFU/mL) level of P. gingivalis significantly increased platelet expression of CD62P in ADP treated and untreated whole blood. In addition, platelet-neutrophil interactions were significantly increased after ADP stimulation, following 5-22 min preincubation of blood with high P. gingivalis CFU. However, in the absence of added ADP, platelet-neutrophil interactions increased in a manner dependent on the preincubation time with P. gingivalis. Moreover, after ADP addition, 16 min preincubation of whole blood with P. gingivalis led to increased labeling of neutrophil-associated DNA. Taken together, the results suggest that the presence of P. gingivalis alters platelet and neutrophil responses to increase platelet activation, platelet interactions with neutrophils, and the level of neutrophil antimicrobial NETs.
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  zzm321990Porphyromonas gingivaliszzm321990; flow cytometry; platelet activation; platelet-neutrophil interaction; thrombosis

Mesh:

Year:  2021        PMID: 33811483      PMCID: PMC9281108          DOI: 10.1111/omi.12336

Source DB:  PubMed          Journal:  Mol Oral Microbiol        ISSN: 2041-1006            Impact factor:   4.107


  69 in total

1.  Src family kinases mediate neutrophil adhesion to adherent platelets.

Authors:  Virgilio Evangelista; Zehra Pamuklar; Antonio Piccoli; Stefano Manarini; Giuseppe Dell'elba; Romina Pecce; Nicola Martelli; Lorenzo Federico; Mauricio Rojas; Giorgio Berton; Clifford A Lowell; Licia Totani; Susan S Smyth
Journal:  Blood       Date:  2006-11-09       Impact factor: 22.113

2.  Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood.

Authors:  Stephen R Clark; Adrienne C Ma; Samantha A Tavener; Braedon McDonald; Zahra Goodarzi; Margaret M Kelly; Kamala D Patel; Subhadeep Chakrabarti; Erin McAvoy; Gary D Sinclair; Elizabeth M Keys; Emma Allen-Vercoe; Rebekah Devinney; Christopher J Doig; Francis H Y Green; Paul Kubes
Journal:  Nat Med       Date:  2007-03-25       Impact factor: 53.440

3.  In vivo tracking of platelets: circulating degranulated platelets rapidly lose surface P-selectin but continue to circulate and function.

Authors:  A D Michelson; M R Barnard; H B Hechtman; H MacGregor; R J Connolly; J Loscalzo; C R Valeri
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

4.  The origin of P-selectin as a circulating plasma protein.

Authors:  R Fijnheer; C J Frijns; J Korteweg; H Rommes; J H Peters; J J Sixma; H K Nieuwenhuis
Journal:  Thromb Haemost       Date:  1997-06       Impact factor: 5.249

5.  Intravascular neutrophil extracellular traps capture bacteria from the bloodstream during sepsis.

Authors:  Braedon McDonald; Rossana Urrutia; Bryan G Yipp; Craig N Jenne; Paul Kubes
Journal:  Cell Host Microbe       Date:  2012-09-13       Impact factor: 21.023

6.  The basis examination of leukocyte-platelet aggregates with CD45 gating as a novel platelet activation marker.

Authors:  A Nagasawa; K Matsuno; S Tamura; K Hayasaka; C Shimizu; T Moriyama
Journal:  Int J Lab Hematol       Date:  2013-01-29       Impact factor: 2.877

7.  Endocarditis pathogen promotes vegetation formation by inducing intravascular neutrophil extracellular traps through activated platelets.

Authors:  Chiau-Jing Jung; Chiou-Yueh Yeh; Ron-Bin Hsu; Chii-Ming Lee; Chia-Tung Shun; Jean-San Chia
Journal:  Circulation       Date:  2014-12-19       Impact factor: 29.690

8.  Clinical isolates of Enterococcus faecalis aggregate human platelets.

Authors:  Magnus Rasmussen; Daniel Johansson; Sara K Söbirk; Matthias Mörgelin; Oonagh Shannon
Journal:  Microbes Infect       Date:  2010-01-28       Impact factor: 2.700

9.  Expression of functional tissue factor by neutrophil extracellular traps in culprit artery of acute myocardial infarction.

Authors:  Dimitrios A Stakos; Konstantinos Kambas; Theocharis Konstantinidis; Ioannis Mitroulis; Eirini Apostolidou; Stella Arelaki; Victoria Tsironidou; Alexandra Giatromanolaki; Panagiotis Skendros; Stavros Konstantinides; Konstantinos Ritis
Journal:  Eur Heart J       Date:  2015-02-07       Impact factor: 29.983

10.  Measurement of NET formation in vitro and in vivo by flow cytometry.

Authors:  Sakiko Masuda; Sakika Shimizu; Junji Matsuo; Yuka Nishibata; Yoshihiro Kusunoki; Fumihiko Hattanda; Haruki Shida; Daigo Nakazawa; Utano Tomaru; Tatsuya Atsumi; Akihiro Ishizu
Journal:  Cytometry A       Date:  2017-07-17       Impact factor: 4.355

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