Functional characterization of an immunity-related GTPase gene in immune defense from obscure puffer (Takifugu obscurus)

2020 ◽  
Vol 103 ◽  
pp. 248-255
Author(s):  
Sufei Hu ◽  
Yan Shi ◽  
Tie Ding ◽  
Wen Duan ◽  
Ziyue Qiu ◽  
...  
2021 ◽  
Vol 119 ◽  
pp. 104019
Author(s):  
Fan-Xiang Gao ◽  
Wei-Jia Lu ◽  
Yan Shi ◽  
Li Zhou ◽  
Jian-Fang Gui ◽  
...  

2020 ◽  
Vol 106 ◽  
pp. 252-262
Author(s):  
Shengli Fu ◽  
Mingmei Ding ◽  
Junru Wang ◽  
Xiaoxue Yin ◽  
Enxu Zhou ◽  
...  

Reproduction ◽  
2019 ◽  
Vol 158 (4) ◽  
pp. 369-376
Author(s):  
Imke Bommer ◽  
Lorena Juriol ◽  
Damián Muzzio ◽  
Natalin Valeff ◽  
Jens Ehrhardt ◽  
...  

The amniotic fluid provides mechanical protection and immune defense against pathogens to the fetus. Indeed, components of the innate and adaptive immunity, including B cells, have been described in the amniotic fluid. However, limited information concerning phenotype and functionality of amniotic fluid B cells is available. Hence, we aimed to perform a full phenotypical and functional characterization of amniotic fluid B cells in normal pregnancy and in a mouse model of preterm birth. Phenotypic analysis depicted the presence of two populations of amniotic fluid B cells: an immature population, resembling B1 progenitor cells and a more mature population. Further isolation and in vitro co-culture with a bone marrow stroma cell line demonstrated the capacity of the immature B cells to mature. This was further supported by spontaneous production of IgM, a feature of the B1 B cell sub-population. An additional in vitro stimulation with lipopolysaccharide induced the activation of amniotic fluid B cells as well as the production of pro and anti-inflammatory cytokines. Furthermore, amniotic fluid B cells were expanded in the acute phase of LPS-induced preterm birth. Overall our data add new insight not only on the phenotype and developmental stage of the amniotic fluid B1 B cells but especially on their functionality. This provides important information for a better understanding of their role within the amniotic fluid as immunological protective barrier, especially with regard to intraamniotic infection and preterm birth.


2014 ◽  
Vol 47 (1) ◽  
pp. 104-114 ◽  
Author(s):  
Don Anushka Sandaruwan Elvitigala ◽  
Thanthrige Thiunuwan Priyathilaka ◽  
Bong-Soo Lim ◽  
Ilson Whang ◽  
Sang-Yeob Yeo ◽  
...  

2020 ◽  
Vol 477 (7) ◽  
pp. 1261-1286 ◽  
Author(s):  
Marie Anne Richard ◽  
Hannah Pallubinsky ◽  
Denis P. Blondin

Brown adipose tissue (BAT) has long been described according to its histological features as a multilocular, lipid-containing tissue, light brown in color, that is also responsive to the cold and found especially in hibernating mammals and human infants. Its presence in both hibernators and human infants, combined with its function as a heat-generating organ, raised many questions about its role in humans. Early characterizations of the tissue in humans focused on its progressive atrophy with age and its apparent importance for cold-exposed workers. However, the use of positron emission tomography (PET) with the glucose tracer [18F]fluorodeoxyglucose ([18F]FDG) made it possible to begin characterizing the possible function of BAT in adult humans, and whether it could play a role in the prevention or treatment of obesity and type 2 diabetes (T2D). This review focuses on the in vivo functional characterization of human BAT, the methodological approaches applied to examine these features and addresses critical gaps that remain in moving the field forward. Specifically, we describe the anatomical and biomolecular features of human BAT, the modalities and applications of non-invasive tools such as PET and magnetic resonance imaging coupled with spectroscopy (MRI/MRS) to study BAT morphology and function in vivo, and finally describe the functional characteristics of human BAT that have only been possible through the development and application of such tools.


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