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81.
Machnicka B Grochowalska R Bogusławska DM Sikorski AF Lecomte MC 《Cellular and molecular life sciences : CMLS》2012,69(2):191-201
This review focuses on the recent advances in functions of spectrins in non-erythroid cells. We discuss new data concerning
the commonly known role of the spectrin-based skeleton in control of membrane organization, stability and shape, and tethering
protein mosaics to the cellular motors and to all major filament systems. Particular effort has been undertaken to highlight
recent advances linking spectrin to cell signaling phenomena and its participation in signal transduction pathways in many
cell types. 相似文献
82.
Xue B Mizianty MJ Kurgan L Uversky VN 《Cellular and molecular life sciences : CMLS》2012,69(8):1211-1259
Many proteins and protein regions are disordered in their native, biologically active states. These proteins/regions are abundant
in different organisms and carry out important biological functions that complement the functional repertoire of ordered proteins.
Viruses, with their highly compact genomes, small proteomes, and high adaptability for fast change in their biological and
physical environment utilize many of the advantages of intrinsic disorder. In fact, viral proteins are generally rich in intrinsic
disorder, and intrinsically disordered regions are commonly used by viruses to invade the host organisms, to hijack various
host systems, and to help viruses in accommodation to their hostile habitats and to manage their economic usage of genetic
material. In this review, we focus on the structural peculiarities of HIV-1 proteins, on the abundance of intrinsic disorder
in viral proteins, and on the role of intrinsic disorder in their functions. 相似文献
83.
Age is an important risk for autoimmunity, and many autoimmune diseases preferentially occur in the second half of adulthood
when immune competence has declined and thymic T cell generation has ceased. Many tolerance checkpoints have to fail for an
autoimmune disease to develop, and several of those are susceptible to the immune aging process. Homeostatic T cell proliferation
which is mainly responsible for T cell replenishment during adulthood can lead to the selection of T cells with increased
affinity to self- or neoantigens and enhanced growth and survival properties. These cells can acquire a memory-like phenotype,
in particular under lymphopenic conditions. Accumulation of end-differentiated effector T cells, either specific for self-antigen
or for latent viruses, have a low activation threshold due to the expression of signaling and regulatory molecules and generate
an inflammatory environment with their ability to be cytotoxic and to produce excessive amounts of cytokines and thereby inducing
or amplifying autoimmune responses. 相似文献
84.
Over the last two decades the molecular and cellular mechanisms underlying T cell activation, expansion, differentiation,
and memory formation have been intensively investigated. These studies revealed that the generation of memory T cells is critically
impacted by a number of factors, including the magnitude of the inflammatory response and cytokine production, the type of
dendritic cell [DC] that presents the pathogen derived antigen, their maturation status, and the concomitant provision of
costimulation. Nevertheless, the primary stimulus leading to T cell activation is generated through the T cell receptor [TCR]
following its engagement with a peptide MHC ligand [pMHC]. The purpose of this review is to highlight classical and recent
findings on how antigen recognition, the degree of TCR stimulation, and intracellular signal transduction pathways impact
the formation of effector and memory T cells. 相似文献
85.
86.
87.
Blasic JR Lane Brown R Robinson PR 《Cellular and molecular life sciences : CMLS》2012,69(9):1551-1562
Melanopsin-based phototransduction is involved in non-image forming light responses including circadian entrainment, pupil
constriction, suppression of pineal melatonin synthesis, and direct photic regulation of sleep in vertebrates. Given that
the functions of melanopsin involve the measurement and summation of total environmental luminance, there would appear to
be no need for the rapid deactivation typical of other G-protein coupled receptors. In this study, however, we demonstrate
that heterologously expressed mouse melanopsin is phosphorylated in a light-dependent manner, and that this phosphorylation
is involved in regulating the rate of G-protein activation and the lifetime of melanopsin’s active state. Furthermore, we
provide evidence for light-dependent phosphorylation of melanopsin in the mouse retina using an in situ proximity ligation
assay. Finally, we demonstrate that melanopsin preferentially interacts with the GRK2/3 family of G-protein coupled receptor
kinases through co-immunoprecipitation assays. Based on the complement of G-protein receptor kinases present in the melanopsin-expressing
retinal ganglion cells, GRK2 emerges as the best candidate for melanopsin’s cognate GRK. 相似文献
88.
Microautophagy: lesser-known self-eating 总被引:1,自引:1,他引:0
Microautophagy, the non-selective lysosomal degradative process, involves direct engulfment of cytoplasmic cargo at a boundary
membrane by autophagic tubes, which mediate both invagination and vesicle scission into the lumen. With its constitutive characteristics,
microautophagy of soluble substrates can be induced by nitrogen starvation or rapamycin via regulatory signaling complex pathways.
The maintenance of organellar size, membrane homeostasis, and cell survival under nitrogen restriction are the main functions
of microautophagy. In addition, microautophagy is coordinated with and complements macroautophagy, chaperone-mediated autophagy,
and other self-eating pathways. Three forms of selective microautophagy, including micropexophagy, piecemeal microautophagy
of the nucleus, and micromitophagy, share common ground with microautophagy to some degree. As the accumulation of experimental
data, the precise mechanisms that govern microautophagy are becoming more appreciated. Here, we review the microautophagic
molecular machinery, its physiological functions, and relevance to human diseases, especially in diseases involving multivesicular
bodies and multivesicular lysosomes. 相似文献
89.
Chronic granulomatous disease (CGD) is an uncommon congenital immunodeficiency seen approximately in 1 of 250,000 individuals.
It is caused by a profound defect in a burst of oxygen consumption that normally accompanies phagocytosis in all myeloid cells
(neutrophils, eosinophils, monocytes, and macrophages). This “respiratory burst” involves the catalytic conversion of molecular
oxygen to the oxygen free-radical superoxide, which in turn gives rise to hydrogen peroxide, hypochlorous acid, and hydroxyl
radicals. These oxygen derivatives play a critical role in the killing of pathogenic bacteria and fungi. As a result of the
failure to activate the respiratory burst in their phagocytes, the majority of CGD patients suffer from severe recurrent infections
and rather unexplained prolonged inflammatory reactions that may result in granulomatous lesions. Both may cause severe organ
dysfunction depending on the tissues involved. Preventive measures as well as rapid (invasive) diagnostic procedures are required
to successfully treat CGD. Hematopoietic stem cell transplantation may be a serious option in some of the patients. 相似文献
90.
Sieni E Cetica V Mastrodicasa E Pende D Moretta L Griffiths G Aricò M 《Cellular and molecular life sciences : CMLS》2012,69(1):29-40
Cytotoxic T lymphocytes, natural killer cells, and NKT cells are effector cells able to kill infected cells. In some inherited
human disorders, a defect in selected proteins involved in the cellular cytotoxicity mechanism results in specific clinical
syndromes, grouped under the name of familial hemophagocytic lymphohistiocytosis. Recent advances in genetic studies of these
patients has allowed the identification of different genetic subsets. Additional genetic immune deficiencies may also induce
a similar clinical picture. International cooperation and prospective trials resulted in refining the diagnostic and therapeutic
approach to these rare diseases with improved outcome but also with improved knowledge of the mechanisms underlying granule-mediated
cellular cytotoxicity in humans. 相似文献