The Joslin researchers then transplanted these modified human diabetic cells into wounds
in mice models of diabetes that also had suppressed immune systems so that they didn't reject human cells.
«Natural killer cells help to drive inflammation, insulin resistance: Study
in mouse models of diabetes identifies key immune mechanisms in abdominal fat.»
The two labs are now collaborating on further studies of the new enzymes — and the potential benefits of inhibiting them —
in mouse models of diabetes, inflammation and autoimmune disease.
Not exact matches
In the new work, published June 10 in the journal Scientific Reports, Zhao, Reid and colleagues used a highly sensitive probe to measure electrical fields in the corneas of isolated eyes from three different lab mouse models with different types of diabetes: genetic, drug - induced and in mice fed a high - fat die
In the new work, published June 10
in the journal Scientific Reports, Zhao, Reid and colleagues used a highly sensitive probe to measure electrical fields in the corneas of isolated eyes from three different lab mouse models with different types of diabetes: genetic, drug - induced and in mice fed a high - fat die
in the journal Scientific Reports, Zhao, Reid and colleagues used a highly sensitive probe to measure electrical fields
in the corneas of isolated eyes from three different lab mouse models with different types of diabetes: genetic, drug - induced and in mice fed a high - fat die
in the corneas
of isolated eyes from three different lab
mouse models with different types
of diabetes: genetic, drug - induced and
in mice fed a high - fat die
in mice fed a high - fat diet.
Scientists
of the German Center for
Diabetes Research (DZD) led by the German Institute
of Human Nutrition (DIfE) have shown
in a
mouse model that the epigenetic * modification
of the Igfbp2 ** gene observed
in the young animal precedes a fatty liver
in the adult animal later
in life.
In addition to looking at mouse models of diabetes, the researchers also showed that exposure of human pancreatic islet cells — both from healthy donors and from patients with Type 1 diabetes — to fasting - mimicking diet in a dish stimulated insulin productio
In addition to looking at
mouse models of diabetes, the researchers also showed that exposure
of human pancreatic islet cells — both from healthy donors and from patients with Type 1
diabetes — to fasting - mimicking diet
in a dish stimulated insulin productio
in a dish stimulated insulin production.
The new study, using an experimental
mouse model of diabetes, is published online
in the journal PLOS One.
Most importantly, these cells protected
mice from developing
diabetes in a
model of disease, having the critical ability to produce insulin
in response to changes
in glucose levels.
The patch, which feels like a mosquito bite when applied, has already proved effective
in mouse models with type 1
diabetes for up to 9 hours, scientists report online before print
in the Proceedings
of the National Academy
of Sciences.
Studies
in mouse models suggest that BL - 9020 can inhibit beta cell death
in the pancreas, thus preventing full maturation
of Type 1
diabetes.
From the first day
of transplantation, the cells produced insulin
in response to glucose spikes
in the
mice's blood, alleviating the
modeled diabetes.
Morgan Fullerton, lead author
of the study, added: «Unlike the majority
of studies using genetic
mouse models, we haven't deleted an entire protein; we have only made a very minor genetic mutation, equivalent to what might be seen
in humans, thus highlighting the very precise way metformin lowers blood sugar
in Type 2
Diabetes»
«We think that for the first time, we have a
mouse model of anorexia that closely resembles the conditions leading up to the disease
in humans,» said study leader Lori Zeltser, PhD, associate professor
of pathology & cell biology and a researcher
in the Naomi Berrie
Diabetes Center.
In a mouse model of type 1 diabetes, RGS1 affects the population of one type of T cell called a «T follicular helper cell» that is critical for B cells and antibody production, Dr. Kissler and his colleagues reported recently in Genes and Immunit
In a
mouse model of type 1
diabetes, RGS1 affects the population
of one type
of T cell called a «T follicular helper cell» that is critical for B cells and antibody production, Dr. Kissler and his colleagues reported recently
in Genes and Immunit
in Genes and Immunity.
Working
in mice that were put on high - fat diets to
model diabetes, «we demonstrated that obesity increases the expression
of pro-inflammatory genes
in abdominal fat, but not
in other organs such as the liver or muscle, nor
in subcutaneous fat,» says Jongsoon Lee, PhD, Assistant Investigator
in Joslin's Section on Pathophysiology and Molecular Pharmacology and Assistant Professor
of Medicine at Harvard Medical School.
Because PD - L1 / programmed cell death (PD - 1) deficiency accelerates development
of diabetes in mouse models, Nasr et al. hypothesized that a defect
in the PD - L1 / PD - 1 pathway may underpin the hyperglycemia observed
in the nonobese diabetic (NOD)
mouse model.
In the laboratory arm
of the Joslin study, researchers studied a
mouse model of human type 1
diabetes.
Similar findings were present
in the cerebral cortex and other regions
of the brain
in these animals and also found
in several other
mouse models of diabetes.
Harmonising ontological descriptions
of phenotype
in mouse and human and improving links between
mouse model data and human data, using
diabetes and obesity as examples, will increase the relevance
of data that is generated
in mouse studies for clinical studies.
Scientists
in the laboratory
of C. Ronald Kahn, M.D., head
of Joslin's Integrative Physiology and Metabolism research section, found that brain cholesterol synthesis, the only source
of cholesterol for the brain, drops
in several
mouse models of diabetes.
Kissler and his research team are using a
mouse model of type 1
diabetes to see what the genes do
in a living animal.
The experimenters successfully tested the compound
in the two
mouse models «either treating right at the beginning
of diabetes, or for reversal
of toxic effects after three or four months
of diabetes, which is even more difficult,» King says.
After colleagues at Sanofi provided an investigational compound that activates PKM2, the team showed that this compound could stop abnormalities
in mouse podocytes both
in cell culture and
in two
mouse models of diabetes.
In the Joslin study, scientists first examined gene expression in the hypothalamus of a mouse model of insulin - deficient (type 1) diabete
In the Joslin study, scientists first examined gene expression
in the hypothalamus of a mouse model of insulin - deficient (type 1) diabete
in the hypothalamus
of a
mouse model of insulin - deficient (type 1)
diabetes.
The metabolic exploration platform
of ICS has a large expertise
in phenotyping
mouse model for
diabetes, obesity and atherosclerosis.
The research team had already shown that the technique worked
in mice but needed a more accurate
model of human
diabetes and so used dogs.
Studies using a
mouse model of type 1
diabetes highlight a potential role for human adipose stem cells
in treatment regimens and, further, they reveal a secreted factor which has important therapeutic relevance
As Kissler's lab began to examine whether pTregs play a role
in diabetes, the scientists first looked for these cells
in the non-obese
diabetes (NOD)
mouse model of type 1
diabetes.
The researchers followed up to identify markers
of aging
in these cells, using several
mouse models — one with impaired glucose tolerance (a contributor to type 2
diabetes progression) and another that shows markers
of rapid aging.
For example,
in a
mouse model of type 1
diabetes (T1D), it has been shown that microbiomes from males protect female
mice from T1D development (Markle et al. 2013).
Using red blood cells modified to carry disease - specific antigens, a team
of scientists from Whitehead Institute and Boston Children's Hospital have prevented and alleviated two autoimmune diseases — multiple sclerosis (MS) and type 1
diabetes —
in early stage
mouse models.
The center, founded
in 2001, provides novel techniques for studying
mouse models of diabetes and other metabolic disorders.
Marc Claret, head
of the Neuronal Metabolism Control Group at IDIBAPS, adds that «our results also suggest pathological implications
of this animal
model, since a diet rich
in fats makes these
mice more susceptible to developing
diabetes.»
In the mouse model of type 1 diabetes, susceptibility was also associated with variation in CTLA - 4 gene splicing with reduced production of a splice form encoding a molecule lacking the CD80 / CD86 ligand - binding domai
In the
mouse model of type 1
diabetes, susceptibility was also associated with variation
in CTLA - 4 gene splicing with reduced production of a splice form encoding a molecule lacking the CD80 / CD86 ligand - binding domai
in CTLA - 4 gene splicing with reduced production
of a splice form encoding a molecule lacking the CD80 / CD86 ligand - binding domain.
This proposed role for GM1 (and indirectly GD1a) provides a rationale for its potency
in suppressing
diabetes in NOD
mice (10) and disease onset
in other animal
models of autoimmunity.
Autoimmune destruction
of insulin - producing pancreatic β - cells is recognized as the key pathogenic feature
of type 1
diabetes in patients and
in the NOD
mouse model (18).