Our data in
humans and mice show that adipocyte size is a strong predictor of the percentage of macrophages in adipose tissue (Figure 3e).
Humans and mice show significantly different responses to arsenic, but the results are still important, says David Polya at the University of Manchester, UK, who was not involved in the work.
Not exact matches
Now, a new study of wild
mice shows that they, too, can develop signs of domestication — white fur patches
and short snouts — with hardly any
human influence.
A study by researchers at the University of Chicago Medicine
shows that when
mice that are genetically susceptible to developing inflammatory bowel disease (IBD) were given antibiotics during late pregnancy
and the early nursing period, their offspring were more likely to develop an inflammatory condition of the colon that resembles
human IBD.
«Our study
shows that epigenetic drift, which is characterized by gains
and losses in DNA methylation in the genome over time, occurs more rapidly in
mice than in monkeys
and more rapidly in monkeys than in
humans,» explains Jean - Pierre Issa, MD, Director of the Fels Institute for Cancer Research at LKSOM,
and senior investigator on the new study.
«We've been hearing about their potential for more than a decade, but the results have always been in
mice and rats,
and no one has
shown they're safe or effective in
humans long term,» says Robert Lanza of Advanced Cell Technology in Marlborough, Massachusetts, the company that carried out the stem cell intervention.
Duke scientists have
shown that it's possible to pick out key changes in the genetic code between chimpanzees
and humans and then visualize their respective contributions to early brain development by using
mouse embryos.
Although the researchers emphasized that laboratory results involving cell lines
and mice do not necessarily translate to
human treatment, they say their findings
show that new mTOR inhibitors combined with chemotherapy could become a new treatment strategy for T - ALL.
University of California, Irvine neurobiologists Leslie Thompson
and Joseph Ochaba with the Departments of Neurobiology & Behavior
and Psychiatry &
Human Behavior
and their colleagues from UCI
and from Children's Hospital of Philadelphia have
shown that reducing the aberrant accumulation of a particular form of the mutant Huntingtin protein corresponds to improvement in symptoms
and neuroinflammation in HD
mice.
Senior author Madhav Dhodapkar, M.D., the Arthur H.
and Isabel Bunker Professor of Medicine
and Immunobiology,
and chief of Hematology, said the study, using tissue
and blood samples from
humans and mice,
shows that chronic stimulation of the immune system by lipids made in the context of inflammation underlies the origins of at least a third of all myeloma cases.
In experiments conducted on
human lung endothelial cells
and in
mice, the researchers
showed that NS1 caused permeability of the endothelium, which lines the walls of blood
and lymph vessels.
Further research
showed that fetal
mice bred to lack these molecules — like animals lacking MHCI,
and like
humans with autism or schizophrenia — undergo inadequate synaptic pruning in some parts of their brains.
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 production.
Many PD patients typically
show an increase in anxiety
and depression,
and in this respect the SNCA
mouse model did not replicate the
human condition.
The two reports also
showed that Zika virus infected
and damaged neuronal stem cells harvested from
mice and humans.
Scientists have a promising new approach to combating deadly
human viruses thanks to an educated hunch by University of California, Riverside microbiology professor Shou - Wei Ding,
and his 20 years of research on plants, fruit flies, nematodes
and mice to
show the truth in his theory.
This take on Michelangelo's famous Sistine Chapel image symbolizes the link between
human pain patients
and the
mouse model: The lab - designed SPR inhibitor (in green),
shown within the active pocket of SPR itself (in gray with its atomic structure in colored lines), is the «bridge» between the two species.
The factor also protects proteasome function in
human,
mouse and yeast cells when challenged with various proteasome poisons, studies
showed.
The results obtained by Afsaneh Gaillard's team
and that Pierre Vanderhaeghen at the Institute of Interdisciplinary Research in
Human and Molecular Biology
show, for the first time, using
mice, that pluripotent stem cells differentiated into cortical neurons make it possible to reestablish damaged adult cortical circuits, both neuroanatomically
and functionally.
Before Katlyn
showed up at NIH, the doctors there were already well prepared: They had inserted healthy
human ADA genes into a modified
mouse retrovirus — a type of virus that can enter
human cells
and transfer new genetic material right into the DNA strands in their nuclei.
In marked contrast to the widely held notion that the insulin - producing pancreatic beta cell loses function with wear
and tear, the researchers now
show that
mouse and human beta cells are fully functional at advanced age.
Since CGP3466B has already been tested in phase II clinical trials to (unsuccessfully) treat Parkinson's disease
and ALS, it is known to be safe for
humans, but the researchers caution that many more years of studies are needed to definitively
show whether it is effective for preventing cocaine damage, first in
mice, then in
humans.
Now, a new study in
mice shows how a gene, called FOXP2, implicated in a language disorder may have changed between
humans and chimps to make learning to speak possible — or at least a little easier.
Researchers then induced a disease in these
mice that mimics
human MS.. In one genetic group, both males
and females fed a high salt diet
showed worse clinical signs of the disease.
«These results are especially exciting because they
show that we can take findings in the
mouse and possibly apply them at the
human patient population,» said Koenig.
A 2007 study co-authored by Small
shows that exercise improves its function in both
mice and humans.
Pasinetti has
shown that polyphenols in red wine reduce cognitive decline —
and may prevent it — in
mice genetically altered to develop Alzheimer's; he hopes to prescribe red wine (
and grape juice varieties) to
humans in the future.
The
mouse model mimics aspects of the infection in
humans, with high levels of the virus seen in the
mouse brain
and spinal cord, consistent with evidence
showing that Zika causes neurological defects in
human fetuses.
The experimental drug J147 is something of a modern elixir of life; it's been
shown to treat Alzheimer's disease
and reverse aging in
mice and is almost ready for clinical trials in
humans.
Hair thinning in a
human patient
and mouse with inherited loss of function mutations in WNT10A is
shown.
In the new study, Lipton
and his colleagues used
human stem cell
and mouse models to
show exactly how SNO can trigger cell death in Parkinson's disease.
For the animal study, the researchers separated 52
mice with colon cancer tumors into three groups, including a control group
and groups that were fed either the grape compounds or sulindac, an anti-inflammatory drug, which was chosen because a previous study
showed it significantly reduced the number of tumors in
humans.
«Worms,
mice,
humans,
and even fruit flies
show similar effects of intoxication at similar alcohol concentrations,» he says,
and human neurons contain a switch similar to that in C. elegans.
We also
show that the strategy is effective in two additional
mouse models, one representing acute infection in
mouse cells
and the other representing chronic, or latent, infection in
human cells.»
In subsequent experiments, Pissios
and colleagues found that NNMT correlated positively with Sirt1
and a healthy metabolic profile in
mice,
and also
showed that
humans with low cholesterol
and low triglycerides exhibited high levels of NNMT
and Sirt1 in their livers.
While these results have yet to be demonstrated in
humans, recent research has
shown that boosting tissue levels of NAD + can improve health
and reduce metabolic complications in
mice that have been fed a high - fat diet.»
Green fluorescent protein labeling allowed them to see the early development pattern
and show that lncND, which ordinarily is not present in
mice — lncND is present only in some primates including
humans — had a functional effect on development.
The study, published Nov. 17 by Proceedings of the National Academy of Sciences,
shows that triclosan causes liver fibrosis
and cancer in laboratory
mice through molecular mechanisms that are also relevant in
humans.
Work in germ - free
mice shows providing the right
human microbial communities can restore growth, likely by restoring the proper connections between growth hormone
and insulinlike growth factor 1.
Tests in
mice and nonhuman primates had
shown TGN1412 to be safe, but when it was injected into
humans — in a dose less than 1/500 of what was given to monkeys — it caused a massive release of infection - fighting T cells that overstimulated the patients» immune systems, resulting in multiple organ failure.
Using all the existing data that was available, Andrechek, along with MSU doctoral student Daniel Hollern, analyzed 1,172
mouse mammary tumor samples from 26 different preclinical models
and was able to compile one of the largest databases to
show which strains of
mice were best suited to study a particular type of
human breast cancer.
A series of biological analyses of the
mice with Tim - 1
and immune cells isolated from
human donors
showed that Ebola virus directly binds to T - cells through Tim - 1 protein binding
and causes massive inflammation that thwarts the immune system.
Previous studies have
shown the drug to be effective at spurring new bone growth in
mice and in
humans with osteoporosis,
and a U-M research team believes that it may spur new growth in brittle bone disease patients as well.
The blue stains in these developing
mice embryos
show that the
human DNA inserted into the rodents turns on sooner
and is more widespread (right) than the chimp version of the same DNA, promoting a bigger brain.
The study, conducted in both
human and mouse cells,
shows that cancer genomes lose copies of repetitive sequences known as ribosomal DNA.
«Our work outlines the genetic similarities of the tissue
and cells in different types of tumors
and shows the strong relationships
mice can have to other
human cancers too.»
«We can only extrapolate to
humans, but in the
mouse, our data
show that the whole process [of egg maturation] takes 18 to 20 days,
and we can detect this asymmetry by the second or third day of the process.
They also
showed that certain genes
and elements are similar in both species, providing a basis to use the
mouse to study relevant
human disease.
Using a model of Parkinson's disease in which the toxin MPTP, made famous in book «The Case of the Frozen Addicts,» induces Parkinson's - like symptoms in
humans and mice, Dr. Smeyne
showed that
mice infected with H1N1, even long after the initial infection, had more severe Parkinson's symptoms than those who had not been infected with the flu.
«Previous studies in
mice have indicated that bacteria that are able to encroach upon the epithelium might be able to promote inflammation that drives metabolic diseases,
and now we've
shown that this is also a feature of metabolic disease in
humans, specifically type 2 diabetics who are exhibiting microbiota encroachment.»