Not exact matches
The startup describes itself as a deep data platform for the study of
exosomes, which are small lipid vesicles — air - or fluid - filled cavities — that are excreted from
cells and which deliver information that Mantra plans to use to come up with new drug therapies.
The other two major targets in the field, circulating tumor
cells and
exosomes, come with their own challenges.
«There are these microvesicles called «
exosomes» that are actually released from every living
cell in the body.
Those
cells naturally bud off
exosomes — tiny bubbles made of
cell membrane — that carry the virus inside them.
«When we block the path into the
cell, we also block the functional effects of the
exosomes.
How do the
exosomes get into the recipient
cells?
The Lund researchers» discovery is the
exosomes» journey from the sender
cell to the receiver
cell and how the receiver
cell captures and internalizes the
exosomes.
The focus of their research is «
exosomes», small virus - like particles that serve as «transport packages» for genetic material and proteins transmitted between
cells.
In this way, the mechanism by which
exosomes enter
cells resembles the spread of viral infections,» says Helena Christianson, doctoral student in Belting's research team and first author of the study.
The importance of
exosomes in the tumour microenvironment has been demonstrated within the field in recent years, as it has been shown that tumour development is halted if the production of
exosomes inside the cancer
cell is stopped.
The team showed that
exosomes could serve as an efficient carrier of RNAi, given that these nano - sized vesicles easily travel across the body and enter
cells, including cancer
cells.
At first it was thought that only functioned as cellular debris warehouses but in recent years has been that could have an important role as a messenger between
cells of the body and now many groups focus their research on the role that could be played
exosomes in various diseases, including cancer.
The team also showed that the cellular process macropinocytosis, which participates in
cell scavenging nutrients and vesicles, contributes to
exosomes uptake in cancer
cells with mutant KRAS.
These improvements push the boundaries of nucleic - acid detection and fragment sizing, affecting applications such as single -
cell nucleic acid analysis, PCR - free preparation of NGS library preparation, bacterial artificial chromosome clone sizing, and
exosome analysis.
Exosomes are small vesicles which are secreted by all
cells and contain proteins and messenger RNAs and microRNAs.
He's also looking at the impact on the ability of trabecular meshwork
cells to make and send out fluid - filled pockets called
exosomes that may enable the
cells to communicate.
Genetic manipulation of
exosomes, virus - sized particles released by all
cells, may offer a new therapeutic approach to treating pancreatic cancer, according to a study at The University of Texas MD Anderson Cancer Center.
Researchers at the Bellvitge Biomedical Research Institute of Bellvitge, the Catalan Institute of Oncology and the University Hospital of Bellvitge have participated in an international study published in the journal Cancer
Cell that describes how
exosomes secreted by tumor
cells contain protein and microRNA molecules capable of transform neighboring
cells into tumoral
cells promoting tumor growth.
The investigators utilized a targeting method called RNA interference (RNAi) which, when delivered via these natural nanoparticles or
exosomes, zero in on mutant KRAS in pancreas cancer
cells, impacting tumor burden and survival in multiple pancreas cancer models.
In the study,
exosomes, which are generated by all
cells and are naturally present in blood, were modified as «iExosomes,» capable of delivering small RNA to specifically target mutant KRAS, resulting in disease suppression and increased overall survival in mouse models.
According to the head of the research group of chemoresistance and Predictors of tumor response and stromal environment ICO - IDIBELL, Alberto Villanueva, «tumor
exosomes contain certain proteins (Dicer, TRBP and Ago2) able to process microRNAs that can alter the around the tumor
cells transforming them into tumoral
cells.»
Further study is needed to gain a better understanding about whether
exosomes entering
cells via macropinocytosis have other features that could enhance their anti-tumor capabilities.»
The study published in Cancer
Cell shows that
exosomes from tumor
cells of breast cancer (and other tumor types such as ovarian and endometrial) are different in size and composition than those of healthy
cells.
«We identified how CD47 contributes to suppressing
exosomes clearance from circulation, and enhancing their delivery to pancreatic cancer
cells.»
However, in the past decade scientists realized that
exosomes play important roles in many biological functions through capsuling and delivering molecular messages in the form of nucleic acids and proteins from the donor
cells to affect the functions of nearby or distant
cells.
«
Exosomes are minuscule membrane vesicles — or sacs — released from most, if not all,
cell types, including cancer
cells,» said Yong Zeng, assistant professor of chemistry at the University of Kansas.
«The increased number of
exosomes reaching the pancreas may gain further advantage to enter KRAS - associated cancer
cells as a result of enhanced macropinocytosis, which concurs with previous findings,» said Kamerkar.
The researchers hypothesize that the
exosomes caused the hMSCs to differentiate by delivering miRNA into the stem
cells.
Tufts University biomedical engineers recently published the first report of a promising new way to induce human mesenchymal stem
cells (or hMSCs, which are derived from bone marrow) to differentiate into neuron - like
cells: treating them with
exosomes.
Exosomes had not previously been studied as a way to induce human stem
cell differentiation.
«New way to repair nerves: Using
exosomes to hijack
cell - to -
cell communication.»
Exosomes are very small, hollow particles that are secreted from many types of
cells.
In a series of experiments reported in PLOS ONE in August, the Tufts researchers showed that
exosomes from PC12
cells (neuron - like progenitor
cells derived from rats) at various stages of their own differentiation could, in turn, cause hMSCs to become neuron - like
cells.
The biomedical engineers also showed that the
exosomes contain miRNAs — tiny pieces of RNA that regulate
cell behavior and are known to play a role in neuronal differentiation.
In lab experiments, the researchers isolated
exosomes from specialized human cardiac stem
cells and found that
exosomes alone had the same beneficial effects as stem
cells.
Exosomes transport small pieces of genetic material, called microRNAs, that enable
cells to communicate with neighboring
cells to change their behavior.
«The concept of
exosome therapy is interesting because it could potentially shift our strategy from living -
cell transplantation to the use of a non-living agent,» he added.
We have found that
exosomes and the cargo they contain are crucial mediators of stem
cell - based heart regeneration, and we believe this might lead to an even more refined therapy using the «active ingredient» instead of the entire stem
cell,» said Eduardo Marbán, MD, PhD, director of the Cedars - Sinai Heart Institute and a pioneer in developing investigational cardiac stem
cell treatments.
«The
exosomes appear to contain the signaling information needed to regenerate healthy heart tissue, they are naturally able to permeate
cells, and they have a coating that protects their payloads from degradation as they shuttle from
cell to cell,» said Marbán, senior author of an article in the May 6, 2014 Stem Cell Repo
cell to
cell,» said Marbán, senior author of an article in the May 6, 2014 Stem Cell Repo
cell,» said Marbán, senior author of an article in the May 6, 2014 Stem
Cell Repo
Cell Reports.
Dr. Batrakova's group investigates the development of personalized drug delivery systems, including using living
cells or
exosomes released from these
cells that are loaded with therapeutics.
Exosomes — small, membrane - derived extracellular vesicles capable of carrying diverse biological cargo including proteins and microRNAs — have been found in a broad range of biological fluids and appear to be predominantly involved in
cell - to -
cell communication.
In addition,
exosomes are being co-opted as a treatment modality and have been modified through their parental
cells to express a targeting moiety or marker tag on their surface.
Insights gained into the underlying biology of metastatic basal
cell carcinoma obtained via
exosome RNA sequencing
The role of rebiopsy and repeat analysis in the setting of post-treatment relapse, along with testing of blood samples for mutations in circulating tumor
cells,
cell free tumor DNA, or
exosomes will be considered.
Recently, however, ephrins and Eph receptors have also been found in extracellular vesicles /
exosomes — small droplets of fat released by
cells, used as transport vehicles, signal transmitters or for eliminating
cell components.
Ephrins and Eph receptors have also been found in the
exosomes of cancer
cells.
They termed these bodies «oviductosomes,» from «oviduct,» which is another name for the fallopian tube, and «
exosomes,» the teeny sacs found in all the body's fluids that help
cells survive.
Intrigued, the Martinsried - based team set up an elaborate experimental study to purify the
exosomes from different
cell types, including neurons, and analyse their contents.
Exosomes form inside
cell compartments and release outside the
cell when these compartments fuse with the
cell's surrounding membrane.
According to Haughey, after many failed experiments to determine the brain's messenger, he visited his colleague and collaborator Daniel Anthony at Oxford University, who introduced him to the concept of «
exosomes» — miniature vesicles released from
cells.