Articles tagged with Stem Cell Research
A team of researchers has discovered multipotent stem cells in deer antlers, which can differentiate into multiple cell types and have the potential to treat various injuries in veterinary medicine. The study highlights a novel source of stem cells for use in regenerative therapies.
Researchers at IUPUI have successfully differentiated human induced pluripotent stem cells into retinal cells using chemical methods, eliminating the need for animal products. This breakthrough could lead to new treatments for retinal diseases and expand the clinical use of regenerative human cells.
Johns Hopkins researchers have discovered that mesenchymal stem cells derived from human adipose tissue can seek out and destroy glioblastoma cancer cells in the brain. This innovative approach may provide a new tool for accessing difficult-to-reach areas of the brain where cancer cells proliferate.
Researchers have found that a signaling molecule called SDF-1 helps stem cells survive in the low-oxygen environment of bone marrow by activating autophagy, a survival pathway. However, with age or disease, SDF-1's role shifts, reducing stem cell survival and increasing the likelihood of fat cell formation.
A novel stem cell niche for the ovarian surface epithelium has been identified, where ovarian carcinoma preferentially originates. This discovery provides a new guide for scientists to look for stem cell niches and sources of cancer in other transitional zones.
Adult stem cells have been identified that can migrate to the intestine and produce intestinal cells, suggesting their potential to treat inflammatory bowel disease. The cells were found to express high levels of a receptor involved in tissue repair and wound closure.
Scientists have developed a web-like scaffold coated with long-sugar molecules that enhances stem-cell cultures and encourages the formation of neuronal cell types. The results, published in the Journal of Biological Chemistry, are promising for treating diseases such as Alzheimer's and diabetes.
OHSU scientists have made a breakthrough by growing human liver stem cells in culture, demonstrating their therapeutic potential. The study's findings suggest that these cells can be infinitely expanded and converted into functional liver cells, offering new hope for treating chronic liver diseases.
Scientists found that distinct niches exist in bone marrow to nurture different types of blood stem cells, which could improve the success of stem cell transplants and chemotherapy. The discovery suggests that targeting specific support cells may be therapeutic for treating certain cancers.
Researchers at UT Southwestern Medical Center have discovered an osteoblastic niche in the bone marrow that nurtures early lymphoid progenitors, specialized blood-forming cells responsible for producing T cells and B cells. This finding may lead to improved safety and effectiveness of bone-marrow transplants and treatments for illnesse...
Researchers used a 'homing' signal to activate stem cells in heart failure patients, improving symptoms and heart function. The study found that 50% of patients showed positive effects one year after treatment, indicating potential for this therapy to widely treat heart failure patients.
Researchers developed an artificial brain system that enables robots to learn and understand new sentences containing a new grammatical structure. This technology has the potential to contribute to understanding linguistic malfunctions in Parkinson's disease and improve robots' ability to acquire language knowledge.
Researchers at Queen's University Belfast are developing a novel approach to repair damaged blood vessels in the retina using adult stem cells. This innovative therapy has the potential to prevent and/or reverse diabetic retinopathy, reducing the risk of vision loss.
Researchers at Penn Vet have identified a new pathway for stimulating bone growth using the protein Jagged-1. This discovery has the potential to treat bone fractures and improve outcomes for patients with rare metabolic conditions like Alagille syndrome.
Researchers compared ASCs and BMSCs from an elderly male donor to treat myocardial infarction in a rat model, finding that ASCs preserved more cardiac function. The study suggests age and health status of cell donors may impact the efficacy of stem cells in treating myocardial infarction.
Scientists have identified a natural trigger that enables stem cells to develop into different cell types in the body, including liver and brain cells. The discovery of protein Tcf15 could help improve techniques for turning stem cells into other cell types in the laboratory.
Scientists describe key details about the structure of transcription factor Oct4, crucial for cellular reprogramming. The study's findings may pave the way for medical applications in regenerative medicine and drug discovery.
Researchers have successfully printed human embryonic stem cells using a novel valve-based technique, enabling the creation of three-dimensional tissues and structures. The breakthrough could speed up drug testing and pave the way for transplantable organs without donation.
Researchers at Duke University Medical Center have found that epidermal growth factor speeds the recovery of blood-making stem cells after exposure to radiation. The finding could lead to new treatments for cancer patients and those affected by dirty bombs or nuclear disasters.
Researchers at the University of California, Berkeley have discovered a sirtuin protein that can reverse age-related degeneration in mice by rejuvenating aged blood stem cells. The study provides new hope for targeted treatments for age-related diseases and opens up possibilities for a 'molecular fountain of youth'.
Research reveals diabetes disrupts bone marrow's ability to produce and repair stem cells, exacerbating cardiovascular disease. MicroRNAs play a crucial role in this process, and targeting them may offer new treatments for diabetic patients.
The study reveals that the Notch protein activates GATA2 gene to produce hematopoietic stem cells and regulates its expression through HES-1 repressor. This basic circuit is essential for generating limited production of GATA2, necessary for hematopoietic stem cell production.
Researchers discovered zebrafish stem cells can selectively regenerate damaged photoreceptor cells, including cones that provide daytime colour vision. This breakthrough could lead to new hope for human eyesight restoration through stem cell therapy.
Researchers at Monash University successfully derived and purified lens epithelium, paving the way for testing new drugs on human tissue. The breakthrough could lead to cures for congenital sight impairment caused by lens damage, particularly in developing countries.
Researchers from Arunachal Pradesh and the Research Institute of World's Ancient Traditions Cultures and Heritage successfully isolated dormant TB bacteria from CD271+ stem cells in bone marrow. The study provides evidence that TB bacteria hide in these stem cells to escape drug treatment, making it difficult to eradicate the disease.
Researchers found that stem cell therapy stimulates the heart's natural repair mechanism, boosting production of adult heart cells and recruitment of existing stem cells. The treatment enhances heart structure and function, with new muscle formed being functional and durable.
A study published in BioMed Central's Stem Cell Research & Therapy journal found that stem cells from bone marrow or fat improved brain and nerve repair after stroke in rats. The treated animals showed significant functional recovery, even without the stem cells migrating to the damaged area.
Researchers found a subset of leukemia cells with slower metabolism, allowing them to survive better. An experimental drug tailored to this unique status is being tested for its ability to attack the disease.
Researchers at the University of Edinburgh discovered that bacteria can change the properties of supporting cells within the nerve system, called Schwann cells, to mimic stem cells. This process enables bacteria to spread throughout the body and potentially aid research into degenerative conditions.
Researchers at North Carolina State University found that the lack of Sp2 protein disrupts neural stem cell division and leads to a decline in neurons in the developing and postnatal brain. This discovery could have implications for understanding neurodevelopmental diseases and regenerative medicine.
Stem-cell therapy has been shown to prevent the decline in heart function associated with Duchenne muscular dystrophy. The treatment involves transplanting stem cells derived from normal mouse blood vessels into the hearts of mice with DMD, where it prevents dilated cardiomyopathy and promotes angiogenesis.
The Jordan Baruch Stem Cell Research Fund was dedicated at Ben-Gurion University to support scholarly collaboration and the Center for Regenerative Medicine, Cellular Therapy and Stem Cell Research. The fund aims to develop treatments for debilitating diseases such as diabetes, ALS, Parkinson's, and leukemia.
Researchers used iPSCs to study the physiological basis of arrhythmias in a patient with LQTS. The results identified a specific regimen for correcting aberrant ion channel activity, offering promise for individualized drug therapies.
Scientists at the University of Granada have found that only a specific group of cord blood stem cells (CB-SC) maintained in culture are useful for therapeutic purposes. The researchers identified Wharton's jelly stem cells (HWJSC) as the most suitable subgroup, which can develop into several types of tissue and modulate immune responses.
A new method of generating stem cells could significantly enhance drug screening and treatment for diseases such as Huntington's and Parkinson's. Researchers developed water-based gels that support the growth of human embryonic stem cells, reducing damage and increasing efficiency.
Researchers from RIKEN have successfully created cancer-specific, immune system cells called killer T lymphocytes from induced pluripotent stem cells. These cells can potentially serve as a cancer therapy in the future, overcoming limitations of lab-produced killer T cells with short lifespan.
Scientists successfully regenerate patients' immune cells using stem cell technology, creating long-lived and targeted cells to combat cancer and viral infections. The findings could lead to the development of strategies to rejuvenate exhausted immune responses.
Researchers from Scotland have demonstrated a way to sort embryonic stem cells based on their electrical properties. The method uses electric fields to differentiate between undifferentiated and differentiated stem cells, which can be useful for biomedical research and potential treatments of diseases like Parkinson's.
Researchers at UNC School of Medicine identified polycomb-like proteins as key regulators in stem cell development and cancer. The study found that these proteins interact with epigenetic signals to control gene expression, implications for both stem cell biology and cancer development.
Researchers found that transplanting neural stem cells into mice with familial ALS slowed disease onset and progression, improved motor function, and extended survival. The study suggests targeting detrimental roles played by non-neuronal cells to develop more effective therapeutics.
Researchers have successfully transferred the nucleus of a healthy egg cell into an egg cell with mutant mitochondrial DNA, effectively eliminating the disease-causing genetic material. The technique has significant implications for preventing mitochondrial disorders, which affect approximately 1 in 10,000 people worldwide.
Researchers from NYSCF and CUMC developed a technique to transfer human egg cells' nuclei, eliminating the inheritance of mitochondrial diseases. This method demonstrates permanent elimination of mitochondrial DNA, preventing future generations from developing these devastating diseases.
A new selective target in muscle regeneration has been identified by researchers at the Bellvitge Biomedical Research Institute. The association of alpha-enolase protein and plasmin plays a crucial role in regulating immune cell attraction and formation of new muscle tissue from stem cells.
The UK government has awarded £6 million to the XMaS facility at the European Synchrotron Radiation in Grenoble, allowing it to continue delivering world-class science. This funding will enable researchers to study the atomic and magnetic structures of materials and their properties under different conditions.
A Cedars-Sinai physician-scientist is leading a research study on Charcot-Marie-Tooth disease, the most common inherited neurological disorder, using induced pluripotent stem cells. The goal of the study is to determine if personalized stem cell lines can be generated for individual patients and potentially cure the disease.
Researchers found that tyrosine kinase inhibitor-resistant leukemia stem cells accumulate DNA damage, potentially leading to disease relapse. Identifying this source of genomic instability may help develop new treatment strategies against CML and other resistant diseases.
Researchers have successfully transplanted stem cells from monkeys into testicular tissue, allowing sperm production to resume and restoring fertility. This breakthrough could provide a new option for male cancer patients who are rendered infertile by chemotherapy and radiation treatments.
Researchers have made significant breakthroughs in optimizing stem cells and transplant approaches to treat patients with blood disorders. A new study has shown that the addition of vorinostat to standard therapy can safely reduce the incidence and severity of graft-versus-host disease, a life-threatening complication associated with h...
Scientists have identified an 'immune system kill switch' that triggers the destruction of blood stem cells in response to severe stress, such as chemotherapy or systemic infections. Blocking this internal signal could prevent death after chemotherapy and boost recovery from infection.
University of Rochester Medical Center scientists have discovered a new approach to speed up blood stem cell recovery after a vulnerable period following a stem-cell transplant. Prostaglandin E2 boosts blood production and protects the surrounding microenvironment, offering new hope for patients with leukemia or other blood disorders.
Researchers at the Salk Institute developed a new technique called indirect lineage conversion (ILC), which allows for faster and safer production of stem cells. ILC reduces production time by over half, from two months to two weeks, and increases cell yields, making it a promising step towards regenerative medicine therapies.
A new study published in PLOS ONE reveals that human stem cells are resistant to human cytomegalovirus (HCMV), a leading cause of congenital intellectual disability and deafness. The research findings suggest that HCMV infection distorts cell differentiation, leading to impaired brain maturation and intellectual ability.
Researchers found that both skeletal muscle MSCs and adipose tissue MSCs improved left ventricle function and reduced infarct size after injection into the heart of laboratory rats. The study suggests that these cells may be a potential treatment modality for patients with acute myocardial infarction.
The new consensus statement from the Hinxton Group highlights the tension between intellectual property policies and scientific norms in East Asia. Japan and China are underrepresented in patents and licensing, but have strengths in national health care systems that could benefit stem cell-based therapies.
Scientists at Johns Hopkins Medicine have successfully used human stem cells to test how diseased cells respond to drugs, paving the way for faster and cheaper drug development. The study identified a promising compound for treating Riley-Day syndrome and demonstrated the potential for tailored treatments for individual patients.
Scientists from the Danish Stem Cell Center found that stem cells grow better in three-dimensional environments, leading to improved insulin-producing cell development. This discovery holds promise for improving diabetes treatment with cell therapy.
Scientists at Stanford Medicine have found a way to let the body direct differentiation of transplanted stem cells without forced manipulation. This breakthrough could speed FDA approval and enable new therapies using pluripotent stem cells.
Researchers at Yale University have discovered that genetic variations are common in the body's tissues, with 30% of skin cells harboring copy number variations. This finding has significant implications for genetic screening and our understanding of human development and disease.
Researchers have developed a safe co-culture system using human umbilical cord blood cells to support the expansion of human embryonic stem cells. This method eliminates the risk of tumor formation associated with traditional feeder cultures, making it a more feasible option for cell transplantation.
A recent study published in the British medical journal 'Clinical & Experimental Allergy' found that children with skin manifestations have increased levels of eosinophil progenitors in their blood. Exposure to environmental contaminants, such as cigarette smoke, was also linked to higher levels of allergy-relevant stem cells.