Scientists publishing in Nature Communications report that they have developed a mini working replica of the female reproductive tract
using human and mouse tissue.
Not exact matches
It has been predicted already that by 2020, we will be
using gesture control on computers to stop us
using our
mouse and keypad,
and that there will be a rise in robotics carrying out
human work in an office environment.
Currently SQZ is developing its technology further
using mouse models
and human blood experiments to understand its mechanisms of action more fully.
Of course, there is still a long way to go before this particular method will be tested on
humans (it was tested on
mice),
and an even longer way to go before it'll be
used in medical therapies (if it ever will translate into therapies), but one thing is becoming clear: We need not compromise our moral principles
and rush into government - funded embryo - destructive research.
The researchers
used specially born
and raised
mice having no gut microbes of their own, that then receive a transplant of 14 bacteria that normally grow in the
human gut.
Data from experiments on phytic acid
using mice and other rodents can not be applied to
humans.
Hassles such as buying paper towels or searching for the perfect
used car that
used to require legwork,
human interaction,
and possibly even wearing pants can now be done with a click of a
mouse from one's own living room.
Mice ranged in age from a few months to almost three years, monkeys from less than one year to 30 years,
and humans from age zero to 86 years (cord blood was
used to represent age zero).
He
and some colleagues are already attempting to
use human organoids to plug stomach holes in
mice.
Shukla
and colleagues discovered that a small drug molecule called BX795, which is sold to labs for
use in experiments, helped clear HSV - 1 infection in cultured
human corneal cells, in donated
human corneas,
and in the corneas of
mice infected with HSV - 1.
The behavioral tests
used here modeled one dimension of the disease — an inability to experience pleasure from normal activities — but not others, such as stress
and anxiety,
and probably tap into different brain mechanisms in
mice than in
humans, he says.
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.
Like the Rosetta Stone that scholars
used to decode hieroglyphics, researchers trained the algorithm with more than 4,600 T cell receptors
and then
used it to correctly assign 81 percent of the
human T cells
and 78 percent of
mouse T cells to one of 10 different viral epitopes.
Dr Luis Pedro Coelho, commented: «These findings suggest that dogs could be a better model for nutrition studies than pigs or
mice and we could potentially
use data from dogs to study the impact of diet on gut microbiota in
humans,
and humans could be a good model to study the nutrition of dogs.
Using the modified system,
human melanoma
and breast cancers as well as
mouse melanoma cells were diagnosed with greater ease
and efficiency.
«The
mouse is one of the most utilised models for studying
human biology
and we
use it for creating models of
human illnesses
and testing new drugs
and therapies.
But it was another three decades before Klassen — who has
used retinal progenitor cells to restore vision in
mice, cats, dogs
and pigs — could conduct
human trials involving retinitis pigmentosa.
The UT Southwestern group had previously
used CRISPR - Cas9, the original gene - editing system, to correct the Duchenne defect in a
mouse model of the disease
and in
human cells.
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.
Many universities
and pharmaceutical companies are engaged in research
and development
using genetically modified
mice that have certain genes manipulated to reproduce
human diseases.
Part of the problem, he says, is that the incidence of many
human chronic diseases rises with age, yet many researchers prefer
using young
mice because of the pressures of being published
and getting funding.
Professor Chayama
and his research group
used mice with «humanized» livers,
and injected them with
human blood.
Using the new gene - editing enzyme CRISPR - Cpf1, researchers at UT Southwestern Medical Center have successfully corrected Duchenne muscular dystrophy in
human cells
and mice in the lab.
Currently, Deng's laboratory is conducting additional preclinical studies
using the
human - derived stem cells from Down syndrome patients
and mouse models to determine whether cellular
and behavioral abnormalities can be improved with minocycline therapy
and other candidate drugs.
Already, researchers have
used CRISPR / Cas9 to edit genes in
human cells grown in lab dishes, monkeys (SN: 3/8/14, p. 7), dogs (SN: 11/28/15, p. 16),
mice and pigs (SN: 11/14/15, p. 6), yeast, fruit flies, the worm Caenorhabditis elegans, zebrafish, tobacco
and rice.
While
mouse models have traditionally been
used in studying the genetic disorder, Deng said the animal model is inadequate because the
human brain is more complicated,
and much of that complexity arises from astroglia cells, the star - shaped cells that play an important role in the physical structure of the brain as well as in the transmission of nerve impulses.
In the current work, they
used a new variation of the gene - editing system to repair the defect in both a
mouse model
and in
human cells.
In their study, Stephanie Cherqui, PhD, associate professor in the UC San Diego School of Medicine Department of Pediatrics,
and colleagues
used a transgenic
mouse model that expresses two mutant
human FXN transgenes,
and exhibits the resulting progressive neurological degeneration
and muscle weakness.
Anatomical examination of
human and mouse eyes was
used to determine the effect of the laser on the sensitive light - detecting retina.
HeLa allowed researchers to study polio, measles, papilloma virus (HPV), HIV
and tuberculosis; it was
used to create the first
human -
mouse cell hybrid,
and even sent into space.
Using the supercomputers at Almaden
and Lawrence Livermore National Laboratory, the group simulated networks that crudely approximated the brains of
mice, rats, cats
and humans.
All animals
use the same enzyme to create the same methylation mark as a signal for gene repression,
and her colleagues who study epigenetics in
mice and humans are excited about the new findings, Strome said.
Using a
mouse model of HSV - 1 as well as autopsied samples of
human adult
and fetal tissues, investigators from Dartmouth College's Geisel School of Medicine found that antibodies against HSV - 1 produced by adult women or female
mice could travel to the nervous systems of their yet unborn babies, preventing the development
and spread of infection during birth.
The
mice were examined with ultrasound echocardiography before
and after the three - month treatment period —
using metrics closely paralleling those
used in
humans.
Microbeads coated in a
human egg protein work as a contraceptive in
mice and could also be
used to select the best sperm for IVF
They injected the particles directly into
mice with an experimental
human brain cancer,
and into the brains of healthy
mice for
use as comparison.
Since the current work was done in
mice, O'Leary
and Zembrzycki want to confirm the link in
humans by
using brain scans to measure the natural variation in the neocortical areas
and search for potential links to disease.
If the drug is deemed safe
and the role of Oprl1 in
humans mimics that seen in
mice, Ressler would move toward testing how it could be
used to prevent PTSD.
The researchers
used «humanized
mice,» which have had their immune systems replaced with
human immune system cells, thymus tissue
and bone marrow.
The group has already started tweaking
human iPS cells
using the same genes that Saitou pinpointed as being important in
mouse germ - cell development, but both Saitou
and Hayashi know that
human signalling networks are different from those in
mice.
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.
«These two studies highlight the value of
using an integrated multi-systems approach — including fruit flies,
mice,
and human cells — to discover mechanisms underlying disease processes.»
Most animal studies of the disease are conducted with laboratory
mice that have been genetically engineered
and bred to model ALS, but for this research, investigators
used rats with ALS because they more accurately portray the disease's variable course in
humans.
Starting in the mid-2000s, Yoshiki Sasai's team at the RIKEN Center for Developmental Biology in Kobe, Japan, demonstrated how to grow brainlike structures
using embryonic stem cells, first from
mice and then
humans.
IVF has long been
used in
humans,
mice and other mammals.
But little is known about the early developmental stages of
human gametes — owing to the sensitivity of working with
human tissue —
and most work in this area has been conducted
using mice.
We can
use clues from similarities with the
mouse and human genomes.
The dosages
used in
human executions are, in some cases, lower by body weight than the dosages that would kill only 50 percent of
mice and from which monkeys have been able to successfully recover.
Researchers developed a new type of cell transplantation to treat
mice mimicking a rare lung disease that one day could be
used to treat this
and other
human lung diseases caused by dysfunctional immune cells.
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.