Type II PtdInsP kinases: location, regulation and function

2007 ◽  
Vol 74 (1) ◽  
pp. 149 ◽  
Author(s):  
Jonathan P. Richardson ◽  
Jonathan H. Clarke ◽  
Katherine A. Hinchliffe ◽  
Robin F. Irvine
Keyword(s):  
Type Ii ◽  
2011 ◽  
Vol 51 (4) ◽  
pp. 423-428 ◽  
Author(s):  
Reza Sabaghi ◽  
Ahad Sahragard ◽  
Reza Hosseini

Functional and Numerical Responses ofScymnus SyriacusMarseul (Coleoptera: Coccinellidae) to the Black Bean Aphid,Aphis FabaeScopoli (Hemiptera: Aphididae) Under Laboratory ConditionsFunctional and numerical responses are basic to any investigation of predator-prey relationships and key components in the selection of predators for biological control. In this study, functional and numerical responses of the female and male ladybeetles,Scymnus syriacusMarseul to different densities of third instar nymphs ofAphis fabae(i.e.5, 10, 20, 30, 40, 60 and 80) as prey, were studied in a growth chamber (25°C, 65±5% RH and a photoperiod of 16L : 8D h) on the broad bean,Vicia fabaeLinn. Using the logistic regression, a type II functional response for both female and male ladybeetles was determined. Using Nonlinear least-square regression, the searching efficiency (a') and handling times (Th) of the female and male adults were estimated as 0.123±0.006 h, 0.434±0.012 h and 0.115±0.008 h, 0.514±0.016, respectively. The Rogers model was used to estimate the maximum theoretical predations (T/Th) for female and male, which were 55.18 and 46.64, respectively. These results indicated a higher efficiency in female ladybeetles. The reproductive numerical response, in terms of eggs laid, increased curvlinearly with increasing prey density. The reproductive response trend was similar to the shape of the type II functional response. This similarity means both responses are interlinked and function simultaneously. The efficiency of the ingested food conversion (ECI) of the females decreased with prey density, as females laid 25±0.65 eggs when exposed to the highest prey density (80) and 3±0.44 eggs at lowest prey density (5).


2006 ◽  
Vol 75 (2) ◽  
pp. 621-633 ◽  
Author(s):  
Hesham F. Nawar ◽  
Sergio Arce ◽  
Michael W. Russell ◽  
Terry D. Connell

ABSTRACT The structure and function LT-IIa, a type II heat-labile enterotoxin of Escherichia coli, are closely related to the structures and functions of cholera toxin and LT-I, the type I heat-labile enterotoxins of Vibrio cholerae and enterotoxigenic Escherichia coli, respectively. While LT-IIa is a potent systemic and mucosal adjuvant, recent studies demonstrated that mutant LT-IIa(T34I), which exhibits no detectable binding activity as determined by an enzyme-linked immunosorbent assay, with gangliosides GD1b, GD1a, and GM1 is a very poor adjuvant. To evaluate whether other mutant LT-IIa enterotoxins that also exhibit diminished ganglioside-binding activities have greater adjuvant activities, BALB/c mice were immunized by the intranasal route with the surface adhesin protein AgI/II of Streptococcus mutans alone or in combination with LT-IIa, LT-IIa(T14S), LT-IIa(T14I), or LT-IIa(T14D). All three mutant enterotoxins potentiated strong mucosal immune responses that were equivalent to the response promulgated by wt LT-IIa. All three mutant enterotoxins augmented the systemic immune responses that correlated with their ganglioside-binding activities. Only LT-IIa and LT-IIa(T14S), however, enhanced expression of major histocompatibility complex class II and the costimulatory molecules CD40, CD80, and CD86 on splenic dendritic cells. LT-IIa(T14I) and LT-IIa(T14D) had extremely diminished toxicities in a mouse Y1 adrenal cell bioassay and reduced abilities to induce the accumulation of intracellular cyclic AMP in a macrophage cell line.


2020 ◽  
Vol 98 (11) ◽  
pp. 834-839
Author(s):  
Alice G. Vassiliou ◽  
Chrysi Keskinidou ◽  
Anastasia Kotanidou ◽  
Frantzeska Frantzeskaki ◽  
Ioanna Dimopoulou ◽  
...  

Bone morphogenetic proteins (BMPs) were once considered only to have a role in bone formation. It is now known that they have pivotal roles in other organ diseases, including heritable pulmonary arterial hypertension (PAH), where genetic mutations in the type II BMP receptor (BMPR2) are the commonest cause of receptor dysfunction. However, it has also recently been demonstrated that aquaporin 1 (Aqp1) dysfunction may contribute to PAH, highlighting that PAH development may involve more than one pathogenic pathway. Whether reduction in BMPR2 affects Aqp1 is unknown. We therefore studied Aqp1 in BMPR2-silenced human pulmonary microvascular endothelial cells (HPMECs). We demonstrated reduced Aqp1 mRNA, protein, and function in the BMPR2-silenced cells. Additionally, BMPR2-silenced cells exhibited lower expression of BMP-signaling molecules. In conclusion, decreased BMPR2 appears to affect Aqp1 at the mRNA, protein, and functional levels. This observation may identify a contributory mechanism for PAH.


2014 ◽  
Vol 25 (6) ◽  
pp. 753-762 ◽  
Author(s):  
Dana M. Alessi Wolken ◽  
Joseph McInnes ◽  
Liza A. Pon

Whereas actomyosin and septin ring organization and function in cytokinesis are thoroughly described, little is known regarding the mechanisms by which the actomyosin ring interacts with septins and associated proteins to coordinate cell division. Here we show that the protein product of YPL158C, Aim44p, undergoes septin-dependent recruitment to the site of cell division. Aim44p colocalizes with Myo1p, the type II myosin of the contractile ring, throughout most of the cell cycle. The Aim44p ring does not contract when the actomyosin ring closes. Instead, it forms a double ring that associates with septin rings on mother and daughter cells after cell separation. Deletion of AIM44 results in defects in contractile ring closure. Aim44p coimmunoprecipitates with Hof1p, a conserved F-BAR protein that binds both septins and type II myosins and promotes contractile ring closure. Deletion of AIM44 results in a delay in Hof1p phosphorylation and altered Hof1p localization. Finally, overexpression of Dbf2p, a kinase that phosphorylates Hof1p and is required for relocalization of Hof1p from septin rings to the contractile ring and for Hof1p-triggered contractile ring closure, rescues the cytokinesis defect observed in aim44∆ cells. Our studies reveal a novel role for Aim44p in regulating contractile ring closure through effects on Hof1p.


1984 ◽  
Vol 121 (1) ◽  
pp. 215-225 ◽  
Author(s):  
Jamson S. Lwebuga-Mukasa ◽  
Gunilla Thulin ◽  
Joseph A. Madri ◽  
Carolyn Barrett ◽  
Joseph B. Warshaw

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