What causes the beta
cell dysfunction in the first place?
His plans for research in his own lab involve «continuing to look at the mechanisms of T
cell dysfunction in human and mice.
Research Interests: Tumor immunity, T lymphocyte effectors, immunotherapy, T -
cell dysfunction in cancer, myeloid derived suppressor cells (MDSC) and angiogenesis
This suggests to us that B
cell dysfunction in early development may contribute to later mental disorders, a possibility that we believe deserves further exploration in future studies.»
The latter substance, phosphorylated tau, is responsible for neurofibrillary tangles, which are suspected of contributing to the nerve
cell dysfunction in the brain that is responsible for Alzheimer's memory symptoms.
Not exact matches
In contrast, SOM cells are involved in cognition and emotion, and dysfunctions in these cells may contribute to ADHD and schizophrenia.&raqu
In contrast, SOM
cells are involved
in cognition and emotion, and dysfunctions in these cells may contribute to ADHD and schizophrenia.&raqu
in cognition and emotion, and
dysfunctions in these cells may contribute to ADHD and schizophrenia.&raqu
in these
cells may contribute to ADHD and schizophrenia.»
In cell culture, low concentrations of these corrector molecules can reduce mitochondrial impairment and neuronal
dysfunction.
But signs of age - associated
dysfunction in the
cell diminish.
It is these people who develop diabetes, either type 1 or type 2, while others with tougher beta
cells will remain healthy even
in if they suffer from autoimmunity or metabolic
dysfunction of the liver.»
The researchers used several measures to determine whether the stem
cells were effective
in alleviating neuropathic pain and bladder
dysfunction at six months.
«We now have a handle on the detailed structure of a complex web of interactions that causes global
dysfunction in cells resulting
in degeneration of the brain.»
The protein's role
in the pathway leading to memory impairment, however, remained unclear until scientists from IMCB utilised live -
cell imaging techniques to elucidate the mechanism of memory impairment and illustrated how SNX27 attributes to synaptic
dysfunction.
Dysfunction of these
cells, as may occur
in disease, is linked to neurodevelopmental disorders and neurodegenerative conditions.
Physician David Nathan, director of the diabetes center at Massachusetts General Hospital
in Boston, notes
in an email message that «what is ironic here is that [free radicals are] generally thought to be bad
in human diabetes,» because they lead to
dysfunction in the
cells that make insulin and vascular complications.
In March 2016, Penn researchers published a study in Blood that showed long - term ibrutinib treatment reverses the dysfunction of T cells in CLL and that combining CAR therapy with ibrutinib enhanced engineered T cell proliferation in mic
In March 2016, Penn researchers published a study
in Blood that showed long - term ibrutinib treatment reverses the dysfunction of T cells in CLL and that combining CAR therapy with ibrutinib enhanced engineered T cell proliferation in mic
in Blood that showed long - term ibrutinib treatment reverses the
dysfunction of T
cells in CLL and that combining CAR therapy with ibrutinib enhanced engineered T cell proliferation in mic
in CLL and that combining CAR therapy with ibrutinib enhanced engineered T
cell proliferation
in mic
in mice.
Death and
dysfunction of these
cells cause vision loss
in conditions like glaucoma and multiple sclerosis.
«
In these diseases of mitochondrial dysfunction, in a sense, it's a false starvation situation for the cell — there are plenty of nutrients, but because there's a block in the mitochondria's normal function, the mitochondria behave as if there's not enough oxygen,» says Chen, who with Birsoy, authored a paper in the journal Cell Reports describing this wor
In these diseases of mitochondrial
dysfunction,
in a sense, it's a false starvation situation for the cell — there are plenty of nutrients, but because there's a block in the mitochondria's normal function, the mitochondria behave as if there's not enough oxygen,» says Chen, who with Birsoy, authored a paper in the journal Cell Reports describing this wor
in a sense, it's a false starvation situation for the
cell — there are plenty of nutrients, but because there's a block in the mitochondria's normal function, the mitochondria behave as if there's not enough oxygen,» says Chen, who with Birsoy, authored a paper in the journal Cell Reports describing this w
cell — there are plenty of nutrients, but because there's a block
in the mitochondria's normal function, the mitochondria behave as if there's not enough oxygen,» says Chen, who with Birsoy, authored a paper in the journal Cell Reports describing this wor
in the mitochondria's normal function, the mitochondria behave as if there's not enough oxygen,» says Chen, who with Birsoy, authored a paper
in the journal Cell Reports describing this wor
in the journal
Cell Reports describing this w
Cell Reports describing this work.
To find genetic mutations that would rescue the
cells, Chen and Birsoy mimicked mitochondrial
dysfunction in a haploid genetic system developed by former Whitehead Fellow Thijn Brummelkamp.
«
In the study we challenged the view that the age - dependent impairment in glucose homeostasis is solely due to intrinsic, dysfunction of islet cells, and hypothesized that it is instead affected by systemic aging factors,» says first author Joana Almaca at the Diabetes Research Institute, University of Miam
In the study we challenged the view that the age - dependent impairment
in glucose homeostasis is solely due to intrinsic, dysfunction of islet cells, and hypothesized that it is instead affected by systemic aging factors,» says first author Joana Almaca at the Diabetes Research Institute, University of Miam
in glucose homeostasis is solely due to intrinsic,
dysfunction of islet
cells, and hypothesized that it is instead affected by systemic aging factors,» says first author Joana Almaca at the Diabetes Research Institute, University of Miami.
They showed that stress
in pancreatic
cells due to sleep deprivation may contribute to the loss or
dysfunction of these
cells important to maintaining proper blood sugar levels, and that these functions may be exacerbated by normal aging.
One reason group A Streptococcus and other invasive pathogens are so dangerous is they release pore - forming toxins that can poke holes
in the membranes of
cells within a person's body, leading to cellular
dysfunction or
cell death.
While changes
in insulin secretion are unlikely to play a major role
in the acute effects of SD, cellular stress
in pancreatic tissue suggests that chronic SD may contribute to the loss or
dysfunction of endocrine
cells, and that these effects may be exacerbated by normal aging, say the researchers.
In EAE, as with MS, immune
cells attack a nerve
cell protein called myelin, causing symptoms ranging from impaired vision to severe motor
dysfunction and even death.
This would alter ion levels inside the
cells and
in turn trigger neuronal
dysfunction and
cell death.
Kozai explains, «
Dysfunction in glial
cells has been implicated as a cause and / or major contributor to an increasing number of neurological and developmental diseases.
The researchers developed two such signatures from
cells found
in the urine that could differentiate,
in a two - step approach, the common causes of acute kidney
dysfunction with high accuracy.
Published
in Nature Neuroscience, the findings suggest that astrocytes — star - shaped
cells that are abundant
in the brain and support neuronal function — are important regulators of information storage, and their
dysfunction might lead to memory decline
in disease.
For example, how genetic programs affect the function of specific
cell types, how they vary early or later
in life and how
dysfunction in these programs might contribute to disease, all of which could help scientists learn more about the fundamental workings of the brain.
Damage to astrocytes — star - shaped
cells found
in the brain and spinal cord — is found
in many neurodegenerative conditions, but it's been unclear exactly what role astrocyte
dysfunction plays
in the development of disease.
«Our findings define a potential mechanism for neuronal
cell death
in Alexander disease and possibly other neurodegenerative diseases with astrocyte
dysfunction.»
«Each
cell in the kidney seems to have a unique non-redundant function, and
dysfunction of specific
cell types present with specific symptoms
in people.
The researchers discovered that genetic
dysfunction in what they call the HIPPO - TAZ / YAP and Gαs - protein feedback circuit disrupts the balanced production of Schwann
cells.
But there is no doubt that stem
cell therapy will become an important tool
in the treatment of erectile
dysfunction.»
Previous studies suggest that the symptoms of GWI are due to
dysfunction of the mitochondria, the site
in cells where molecules that power the body's processes are produced.
We also demonstrate that NS1 from DENV1, DENV2, DENV3, and DENV4 triggers endothelial barrier
dysfunction, causing increased permeability of human endothelial
cell monolayers
in vitro.
«Stem
cells shown to restore erection capability
in men with erectile
dysfunction.»
The study is published
in the scientific journal Oncoimmunology and describes how a
cell type
in the blood, the neutrophil, causes kidney
dysfunction in mice with cancer.
These
cells were remarkable on their own as they were able to effectively reverse the scarring that contributes to lung
dysfunction and difficulty
in breathing,» he said.
Cholesterol
in β -
cell dysfunction: The emerging connection between HDL cholesterol and type 2 diabetes
Longitudinal studies
in animals that spontaneously develop T2D (nonhuman primates and domestic cats) showed that detection of IAPP aggregates precedes β
cell dysfunction and clinical signs of the disease (Howard, 1986; de Koning et al., 1993; Ma et al., 1998).
However, compelling evidence suggests that accumulation of amyloid aggregates
in the islets of Langerhans might significantly contribute to β
cell dysfunction and disease (Hull et al., 2004; Haataja et al., 2008; Jurgens et al., 2011; Mukherjee et al., 2015).
«It was known that acute exposure to pyrethroids could lead to immune
dysfunction, and that the molecules they act on can be found
in immune
cells; now we need to know more about how longer - term exposure affects the immune system
in a way that increases risk for Parkinson's.»
The overall goal of this research is to provide new insight into the function and
dysfunction of human neural
cell populations
in aging and neurological disorders, such as LOAD, and to identify mechanisms and molecules that can be translated to developing and testing novel diagnostic tools and therapeutics.
Aguirre, J.A.; Kehr, J.; Yoshitake, T.; Liu, F.L.; Rivera, A.; Fernandez - Espinola, S.; Andbjer, B.; Leo, G.; Medhurst, A.D.; Agnati, L.F.; Fuxe, K. Protection but maintained
dysfunction of nigral dopaminergic nerve
cell bodies and striatal dopaminergic terminals
in MPTP - lesioned mice after acute treatment with the mGluR5 antagonist MPEP.
Dysfunction of mitochondria, the energy - generating organelle
in human
cells, is one hypothesis concerning the severe fatigue experienced by ME / CFS patients.
The structural analysis guides further mutagenesis and biochemical experiments
in both reconstituted systems
in vitro and
in primary
cells, to finely analyze the mechanisms that mediate macromolecular function, or lead to a pathological
dysfunction.
We are currently profiling inhibitory interneuron
cell types
in mouse models of AD to identify potential molecular mechanisms of interneuron
dysfunction and potential targets of intervention.
Human iPS
cell - derived hepatocytes differentiated with our robust differentiation protocol and cultured using our novel maintenance medium provide an inexhaustible, consistent supply of functional hepatocytes that can be used to advance the understanding of diseases related to
dysfunction in liver metabolism, including NAFLD / NASH, type 2 diabetes, and metabolic syndrome.
Aging research reveals that some aging phenotypes are reversible,
in fact age related
dysfunctions may be classified
in an early reversible stage, and
in a later stage with permanent damage (DNA mutations or deletions or
cell death) 1.
Nicola Watt (Reichmann, TUD)-- «Mitochondrial
dysfunction and lipid metabolism
in cell culture models of respiratory chain and neurodegenerative diseases» (2007)