Related Experiment Video
Updated: Jan 30, 2026

07:48
Investigating the Function of Coronin A in the Early Starvation Response of Dictyostelium discoideum by Aggregation Assays
Published on: June 18, 2016
7.5K
Coronin-1, King of Alloimmunity
1Emory Transplant Center and Department of Surgery, Emory University, Atlanta, GA, USA.
Immunity
|January 17, 2019
Summary
Researchers identified a coronin-1-PDE4-cAMP pathway that can induce transplantation tolerance without compromising anti-microbial immunity. This discovery offers a precise way to manipulate immune responses for organ transplantation.
Area of Science:
- Immunology
- Transplantation Biology
- Molecular Signaling
Background:
- Precise manipulation of immune responses is crucial for successful organ and tissue transplantation.
- Differentiating between graft-reactive and anti-microbial T cell responses remains a challenge in transplantation immunology.
Purpose of the Study:
- To identify molecular pathways that differentially regulate T cell responses towards transplanted grafts versus pathogens.
- To explore potential therapeutic targets for inducing transplantation tolerance while preserving essential immune functions.
Main Methods:
- Investigated the role of the coronin-1-PDE4-cAMP signaling axis in T cell regulation.
- Utilized experimental models to perturb this pathway and assess its impact on immune responses.
Main Results:
- Identified a specific coronin-1-PDE4-cAMP signaling axis that plays a key role in immune cell function.
- Demonstrated that perturbing this axis can induce transplantation tolerance.
- Showed that this induced tolerance does not impair the ability to mount anti-microbial immune responses.
Conclusions:
- The coronin-1-PDE4-cAMP axis represents a novel target for modulating immune responses in transplantation.
- This pathway offers a potential strategy for achieving transplant tolerance while maintaining host defense against infections.
Related Concept Videos
SN1 Reaction: Stereochemistry
10.3K
This lesson provides an in-depth discussion of the stereochemical outcomes in an SN1 reaction.
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
10.3K
SN1 Reaction: Kinetics
9.6K
In an SN2 reaction, the reaction rate depends on both the type of nucleophile and the substrate. A hindered tertiary alkyl halide is practically inert to the SN2 mechanism despite using a strong nucleophile.
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
9.6K
SN1 Reaction: Mechanism
14.3K
Kinetic studies of ionization of a tertiary halide in a protic solvent suggest that only the substrate participates in the rate-determining step (slow step). The nucleophile is involved only after the slowest step. The SN1 reaction takes place in a multiple-step mechanism.
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
14.3K
Acidity of 1-Alkynes
11.2K
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
11.2K
Predicting Products: SN1 vs. SN2
17.3K
Nucleophilic substitution reactions of alkyl halides can proceed via an SN1 or an SN2 mechanism. While in SN2 reactions, the nucleophile attacks the substrate simultaneously as the leaving group departs, in SN1 reactions, the substrate first dissociates to give the carbocation intermediate. Various factors such as the structure of the substrate, the strength of the nucleophile, and the nature of the solvent promote one mechanism over the other.
With increased substitution on the alkyl halide,...
With increased substitution on the alkyl halide,...
17.3K
Preparation of 1° Amines: Gabriel Synthesis
4.6K
Direct alkylation is not a suitable method for synthesizing amines because it produces polyalkylated products. Gabriel synthesis is the most preferred method to exclusively make primary amines. The method uses phthalimide, which contains a protected form of nitrogen that participates in alkylation only once to predominantly give primary amines.
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
4.6K

