Scientists 3D Bioprint a hybrid tissue construct for cartilage regeneration

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Wake Forest Institute for Regenerative Medicine scientists (WFIRM) have developed a method to bioprint a type of cartilage that could someday help restore knee function damaged by arthritis or injury.

This cartilage, known as fibrocartilage, helps connect tendons or ligaments or bones and is primarily found in the meniscus in the knee. The meniscus is the tough, rubbery cartilage that acts as a shock absorber in the knee joint. Degeneration of the meniscus tissue affects millions of patients and arthroscopic partial meniscectomy is one of the most common orthopedic operations performed. Besides surgery, there is a lack of available treatment options.

In this latest proof-of-concept strategy, the scientists have been able to 3D bioprint a hybrid tissue construct for cartilage regeneration by printing two specialized bioinks – hydrogels that contain the cells – together to create a new formulation that provides a cell-friendly microenvironment and structural integrity. This work is done with the Integrated Tissue and Organ Printing System, a 3D bioprinter that was developed by WFIRM researchers over a 14-year period. The system deposits both biodegradable, plastic-like materials to form the tissue “shape” and bioinks that contain the cells to build new tissues and organs.

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Nanobiologic approach trains the innate immune system to eliminate tumor cells

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A groundbreaking new type of cancer immunotherapy developed at the Icahn School of Medicine at Mount Sinai trains the innate immune system to help it eliminate tumor cells through the use of nanobiologics, tiny materials bioengineered from natural molecules that are paired with a therapeutic component, according to a study published in Cell in October.

This nanobiologic immunotherapy targets the bone marrow, where part of the immune system is formed, and activates a process called trained immunity. This process reprograms bone marrow progenitor cells to produce “trained” innate immune cells that halt the growth of cancer, which is normally able to protect itself from the immune system with the help of other types of cells, called immunosuppressive cells.

This work for the first time demonstrates that trained immunity can be successfully and safely induced for the treatment of cancer. The research was performed in animal models, including a mouse model with melanoma, and the researchers said it is being developed for clinical testing.

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Scientists create artificial, ‘living aneurysm’ outside the human brain in extraordinary first

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 For the first time, researchers have 3D printed a ‘living’ model of an aneurysm outside the body, using human brain cells. The breakthrough could one day assist brain surgeons in both training and high-risk decision-making.

An aneurysm occurs when a bulge or bubble develops at a weak point in a given blood vessel, which can take place in the heart or brain. The weakened wall can eventually rupture, with catastrophic and life-threatening consequences for the patient.

Given the highly sensitive and delicate areas in which aneurysms take place, they are often extremely difficult to both find and treat.

As a potential solution, researchers at the Lawrence Livermore National Laboratory (LLNL), including scientists from Duke University and Texas A&M, have created an external, artificial replica which mimics the particular environment in which aneurysms occur.

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Rapid disease pathogen identification a step closer following successful GeneCapture demonstration

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GeneCapture’s unique disposable cartridge design enables rapid multi-pathogen identification directly from samples.

 Soon it could only take an hour to find out what pathogen is making you ill, following the successful demonstration of the world’s first multi-pathogen identification using non-amplified RNA detection by GeneCapture, a company cofounded by researchers at The University of Alabama in Huntsville (UAH), a part of the University of Alabama System.

GeneCapture has licensed a molecular binding technology from UAH and the company’s CAPTURE PLATFORM is on track for commercialization within two years. The GeneCapture team has briefed the Food and Drug Administration (FDA) on its approach and has begun to prepare for the clinical testing required for FDA clearance. It is in discussions with industry leaders for various applications in health care rapid infection detection.

“We made history today—this is the first time an automated rapid pathogen identification has been reported directly from the RNA of the sample, with no modification or amplification of its genetic source, in about an hour,” says GeneCapture CEO and local entrepreneur Peggy Sammon. “We envision a future where finding out why you are sick can be solved almost anywhere, in an hour, and without being chained to a lab.”

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CRISPR therapy restores retinal and visual function in mice

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A breakthrough study, led by researchers from the University of California, Irvine, results in the restoration of retinal and visual functions of mice models suffering from inherited retinal disease.

Published today in Nature Biomedical Engineering, the paper, titled, “Restoration of visual function in adult mice with an inherited retinal disease via adenine base editing,” illustrates the use of a new generation CRISPR technology and lays the foundation for the development of a new therapeutic modality for a wide range of inherited ocular diseases caused by different gene mutations.

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Coronavirus: test that can detect pathogen in 5 minutes developed by Nobel Prize winner Jennifer Doudna

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The research team was led by University of California, Berkeley’s Dr Jennifer
Doudna, a joint winner of the 2020 Nobel Prize for chemistry. Photo: Reuters

California-based researchers develop a test that can detect the coronavirus using gene-editing technology and a modified mobile phone camera.

Mobile phones were used for ‘their robustness and cost-effectiveness, and the fact that they are widely available’, say the researchers.

A team of California-based researchers have developed a test that can detect the coronavirus in five minutes using gene-editing technology and a modified mobile phone camera, a discovery that could solve the issue of under-testing in epidemic-stricken countries.

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Researchers create hand-held device for patients to read levels of cancer biomarker in their own blood

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Newswise: Researchers create hand-held device for patients to read levels of cancer biomarker in their own blood

Newswise — HAMILTON, ON, Oct. 8, 2020 — Researchers at McMaster and Brock universities have created the prototype for a hand-held device to measure a biomarker for cancer, paving the way for home-based cancer monitoring and to improve access to diagnostic testing.

The device works much like the monitors that diabetics use to test their blood-sugar levels and could be used in a medical clinic or at home, all without lab work, greatly simplifying the process for testing blood for cancer’s signature.

A user would mix a droplet of blood in a vial of reactive liquid, then place the mixture onto a strip and insert it into a reader. In minutes, the device would measure an antigen that indicates the degree to which cancer is present.

The prototype has been designed to monitor prostate specific antigen (PSA) and the technology can readily be adapted to measure other markers, depending on the form of cancer or other chronic disease.

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Scientists claim to invent hydrogel that heals nerve damage

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THEY SAY THE GEL CAN PROPAGATE NEURAL SIGNALS WHERE NERVES ARE INJURED.

A team of doctors and engineers have developed a new hydrogel that they say might be able to repair nerve damage more quickly and reliably than any other methods.

The hydrogel is essentially a porous and water-saturated material that can stretch, bend, and — most importantly — propagate neural signals. In animal trials, the team of Nanjing University researchers found that the hydrogel restored lost bodily function and helped the animals heal faster, according to research published Wednesday in the journal ACS NANO. Now, they’re hoping the gel will work in human medicine as well.

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Biochip innovation combines AI and nanoparticles to analyze tumors

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Electrical engineers, computer scientists and biomedical engineers at the University of California, Irvine have created a new lab-on-a-chip that can help study tumor heterogeneity to reduce resistance to cancer therapies.

In a paper published today in Advanced Biosystems, the researchers describe how they combined artificial intelligence, microfluidics and nanoparticle inkjet printing in a device that enables the examination and differentiation of cancers and healthy tissues at the single-cell level.

“Cancer cell and tumor heterogeneity can lead to increased therapeutic resistance and inconsistent outcomes for different patients,” said lead author Kushal Joshi, a former UCI graduate student in biomedical engineering. The team’s novel biochip addresses this problem by allowing precise characterization of a variety of cancer cells from a sample.

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Neural network trained to control anesthetic doses, keep patients under during surgery

To define how the world should look, neural networks are making up their own rules

 Researchers demonstrate how deep learning could eventually replace traditional anesthetic practices.

Academics from the Massachusetts Institute of Technology (MIT) and Massachusetts General Hospital have demonstrated how neural networks can be trained to administer anesthetic during surgery.

Over the past decade, machine learning (ML), artificial intelligence (AI), and deep learning algorithms have been developed and applied to a range of sectors and applications, including in the medical field.

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Experimental cancer treatment destroys cancer cells without using any drugs

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One of the latest methods pioneered by scientists to treat cancer uses a Trojan horse sneak attack to prompt cancer cells to self-destruct – all without using any drugs.

Key to the technique is the use of a nanoparticle coated in a specific amino acid called L-phenylalanine, one of several such acids that cancer cells rely on to grow. L-phenylalanine isn’t made by the body, but absorbed from meat and dairy products.

In tests on mice, the nanoparticle – called Nano-pPAAM or Nanoscopic phenylalanine Porous Amino Acid Mimic – killed cancer cells specifically and effectively, posing as a friendly amino acid before causing the cells to destroy themselves.

The self-destruction mode is triggered as the nanoparticle puts production of certain chemicals known as reactive oxygen species (ROS) into overdrive. It’s enough to bring down the cancer cells while leaving neighbouring, healthy cells intact.

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3-D bioprinting constructs for cartilage regeneration

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Schematic presentation of the study design and scaffold construction. (A) Schematic Illustration of the study design with 3D bioprinted dual-factor releasing and gradient-structured MSC-laden constructs for articular cartilage regeneration in rabbits. Schematic diagram of construction of the anisotropic cartilage scaffold and study design. (B) A computer-aided design (CAD) model was used to design the four-layer gradient PCL scaffolding structure to offer BMS for anisotropic chondrogenic differentiation and nutrient supply in deep layers (left). Gradient anisotropic cartilage scaffold was constructed by one-step 3D bioprinting gradient polymeric scaffolding structure and dual protein-releasing composite hydrogels with bioinks encapsulating BMSCs with BMP4 or TGFβ3 μS as BCS for chondrogenesis (middle). The anisotropic cartilage construct provides structural support and sustained release of BMSCs and differentiative proteins for biomimetic regeneration of the anisotropic articular cartilage when transplanted in the animal model (right). Different components in the diagram are depicted at the bottom. HA, hyaluronic acid.

 

Cartilage injury is a common cause of joint dysfunction and existing joint prostheses cannot remodel with host joint tissue. However, it is challenging to develop large-scale biomimetic anisotropic constructs that structurally mimic native cartilage. In a new report on Science Advances, Ye Sun and a team of scientists in orthopedics, translational research and polymer science in China, detailed anisotropic cartilage regeneration using three-dimensional (3-D) bioprinting dual-factor releasing gradient-structured constructs. The team used the dual-growth-factor releasing mesenchymal stem cell (MSC)-laden hydrogels for chondrogenic differentiation (cartilage development). The 3-D bioprinted cartilage constructs showed whole-layer integrity, lubrication of superficial layers and nutrient supply into deeper layers. The scientists tested the cartilage tissue in the lab and in animal models to show tissue maturation and organization for translation to humans after sufficient experimental studies. The one-step, 3-D printed dual-factor releasing gradient-structured cartilage constructs can assist regeneration of MSC- and 3-D bioprinted therapy for injured or degenerative joints.

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