scholarly journals Human and Murine Innate Immune Cell Populations Display Common and Distinct Response Patterns during Their In Vitro Interaction with the Pathogenic Mold Aspergillus fumigatus

2017 ◽  
Vol 8 ◽  
Author(s):  
Anna-Maria Hellmann ◽  
Jasmin Lother ◽  
Sebastian Wurster ◽  
Manfred B. Lutz ◽  
Anna Lena Schmitt ◽  
...  
Biologicals ◽  
2015 ◽  
Vol 43 (2) ◽  
pp. 100-109 ◽  
Author(s):  
M.E. Hoonakker ◽  
L.M. Verhagen ◽  
C.F.M. Hendriksen ◽  
C.A.C.M. van Els ◽  
R.J. Vandebriel ◽  
...  

2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Joy M Stanilka ◽  
Cheryl A Rowe ◽  
Rebecca A Creasy ◽  
Xiaoshuang Dai ◽  
Susan S Percival

2012 ◽  
Vol 172 (2) ◽  
pp. 259-260
Author(s):  
A.E. Mendoza ◽  
W.J. Brickey ◽  
C.J. Neely ◽  
J. Ting ◽  
R. Maile ◽  
...  

2019 ◽  
Author(s):  
Galit H. Frydman ◽  
Felix Ellett ◽  
Julianne Jorgensen ◽  
Anika L. Marand ◽  
Lawrence Zukerberg ◽  
...  

AbstractMegakaryocytes (MKs) are precursors to platelets, the second most abundant cells in the peripheral circulation. However, while platelets are known participate in immune responses and play significant roles during infections, the role of MKs within the immune system has not been explored. Here we utilizein vitrotechniques to show that both cord blood-derived MKs (CB MKs) and MKs from a human megakaryoblastic leukemia cell line (Meg-01) chemotax towards pathogenic stimuli, phagocytose bacteria, and release chromatin webs in response to bacteria. Moreover, in patients with sepsis, we found that MK counts were significantly higher in the peripheral blood, and CD61+staining was increased in the kidneys and lungs, correlated with the development of organ dysfunction. Overall, our study suggests that MK cells display basic innate immune cell functions and respond during infections and sepsis.


PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0252642
Author(s):  
Maide Ozen ◽  
Hui Zhao ◽  
Flora Kalish ◽  
Yang Yang ◽  
Lauren L. Jantzie ◽  
...  

Heme oxygenase-1 (HO-1) is an evolutionarily conserved stress response enzyme and important in pregnancy maintenance, fetal and neonatal outcomes, and a variety of pathologic conditions. Here, we investigated the effects of an exposure to systemic inflammation late in gestation [embryonic day (E)15.5] on wild-type (Wt) and HO-1 heterozygous (Het, HO-1+/-) mothers, fetuses, and offspring. We show that alterations in fetal liver and spleen HO homeostasis during inflammation late in gestation can lead to a sustained dysregulation of innate immune cell populations and intracellular myeloid HO-1 expression in the spleen through young adolescence [postnatal day 25] in mice.


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