Thursday, 28 November 2019

Ketogenic diet helps tame flu virus

Mice fed a high-fat, low-carbohydrate diet like the Keto regimen were better able to combat the flu virus than mice fed food high in carbohydrates, according to a new study.

Influenza virus 
Credit@ Axel Kock


The ketogenic diet which includes meat, fish, poultry and non-starchy vegetables activates a subset of T cells in the lungs, enhancing mucus production from airway cells that can effectively trap the virus. 

The ketogenic is a popular diet choice in recent years for those looking to lose weight and show off their abs quickly. A type of immune system activators called inflammasomes can cause harmful immune system responses in their host. Researchers said that a keto diet could help block the formation of inflammasomes. 

Mice fed a ketogenic diet and infected with the influenza virus had a higher survival rate than mice on a high-carb normal diet. The ketogenic diet triggered the release of gamma delta T cells, which produce mucus in the cell linings of the lung which the high-carbohydrate diet did not. 

When mice were bred without the gene that codes for gamma delta T cells, the ketogenic diet provided no protection against the influenza virus. 

This study shows that the way the body burns fat to produce ketone bodies from the food we eat can fuel the immune system to fight flu infection. 

Ref: EL Goldberg, RD Molony, E Kudo, S Sidorov, Y Kong, VD Dixit, A Iwasaki, Ketogenic diet activates protective Gamma Delta T cell responses against influenza virus infection. Science Immunology, 2019; 4(41): eaav2026. 

DOI: 10.1126/sciimmunol.aav2016

Monday, 23 September 2019

Electric tech could help reverse baldness





People worldwide who suffer from pattern baldness are going to be able to reverse the condition due to this noninvasive, low-cost electric technology which can stimulate hair growth

Small device called nano-generators passively gather energy from day-to-day movements and then transmit low-frequency pulses of electricity to the skin. That gentle electric stimulation causes dormant follicles to wake up. It does not require a bulky battery pack or complicated electronics. In fact, they’re so low-profile that they could be used discreetly underneath a cap. This makes it a comfortable device which does not cause any pain or inconvenience associated with the hair restoration surgeries or other treatment procedures. 

Rather than causing the follicles to regenerate on smooth skin, they reactivate the dormant hair-producing structures. Therefore, it should be understood that this technology could be used as an intervention for men who are experiencing the early stages of pattern baldness and not for those who have been bald for a long time.

Tested on hairless mice, the device stimulated hair growth effectively. The researchers have patented the concept with the Wisconsin Alumni Research Foundation, and they hope to move forward with human testing soon. 


Ref: Guang Yao, Dawei Jiang, Jun Li, Lei Kang, Sihong Chen, Yin Long, Yizhan Wang, Peng Huang, Yuan Lin, Weibo Cai, Xudong Wang. Self-Activated Electrical Stimulation for Effective Hair Regeneration via a Wearable Omnidirectional Pulse Generator. ACS Nano, 2019. 

Saturday, 21 September 2019

First hydrogel to repair heart tissue


Scientists successfully conducted a first-in-human, FDA-approved Phase 1 clinical trial of an injectable hydrogel that aims to repair damage and restore cardiac function in heart failure patients who previously suffered a heart attack. After a heart attack, scar tissue develops, which diminishes muscle function and leads to heart failure. This is where VentriGel comes in. Once injected in damaged cardiac muscle, VentriGel forms a scaffold that acts as a reparative environment where healthy cells migrate, leading to increases in cardiac muscle, less scar tissue, and improvements in heart function.


VentriGel was invented by Professor Karen Christman  and her team, then licensed from UC San Diego and developed by Ventrix, Inc, which was cofounded by CEO Adam Kinsey and Christman.

VentriGel is made from cardiac connective tissue taken from pigs, which is stripped of heart muscle cells through a cleansing process. It is then freeze-dried and milled into powder form, and then liquefied into a fluid that can be easily injected into heart muscle in a minimally invasive procedure that does not require surgery. Once it hits body temperature, the liquid turns into a semi-solid, porous gel.

Ventrix is now gearing up for a Phase 2 clinical trial that will expand on this successful first-in-human study.



Ref: Jay H. Traverse, Timothy D. Henry, Nabil Dib, Amit N. Patel, Carl Pepine, Gary L. Schaer, Jessica A. DeQuach, Adam M. Kinsey, Paul Chamberlin, Karen L. Christman. First-in-Man Study of a Cardiac Extracellular Matrix Hydrogel in Early and Late Myocardial Infarction Patients. JACC: Basic to Translational Science, 2019; DOI: 10.1016/j.jacbts.2019.07.012



Thursday, 3 January 2019

World's smallest tic-tac-toe game board made with DNA


An artist's rendering of a game of tic-tac-toe played with DNA tiles.
Credit: Caltech

The researchers used a technique for shaping structures out of strands of DNA, a process known as DNA origami. Unlike previous techniques, a structure once created could not be altered. However, the researchers could reshape an already-constructed DNA structure using this new technique. To demonstrate the powerful new technique, they used it to play game of tic-tac-toe using a DNA board.

Putting the Pieces Together
That swapping mechanism combines two previously developed DNA nanotechnologies.
Both technologies make use of DNA's ability to be programmed through the arrangement of its molecules. Each strand of DNA consists of a backbone and four types of molecules known as bases. These bases adenine, guanine, cytosine, and thymine, abbreviated as A, T, C, and G can be arranged in any order, with the order representing information that can be used by cells, or in this case by engineered nanomachines.
The second property of DNA that makes it useful for building nanostructures is that the A, T, C, and G bases have a natural tendency to pair up with their counterparts. The A base pairs with T, and C pairs with G. By extension, any sequence of bases will want to pair up with a complementary sequence. For example, ATTAGCA will want to pair up with TAATCGT.
However, a sequence can also pair up with a partially matching sequence. If ATTAGCA and TAATACC were put together, their ATTA and TAAT portions would pair up, and the nonmatching portions would dangle off the ends. The more closely two strands complement each other, the more attracted they are to each other, and the more strongly they bond.
The other technology, self-assembling tiles, is more straightforward to explain. Essentially, the tiles, though all square in shape, are designed to behave like the pieces of a jigsaw puzzle. Each tile has its own place in the assembled picture, and it only fits in that spot.
 The result is tiles that can find their designated spot in a structure and then kick out the tile that already occupies that position. They invented the mechanism of tile displacement, which follows the abstract principle of strand displacement but occurs at a larger scale between DNA origami structures. This is the first mechanism that can be used to program dynamic behaviors in systems of multiple interacting DNA origami structures.

Let's Play
To get the tic-tac-toe game started, they mixed up a solution of blank board tiles in a test tube. Once the board assembled itself, the players took turns adding either X tiles or O tiles to the solution. Because of the programmable nature of the DNA they are made from, the tiles were designed to slide into specific spots on the board, replacing the blank tiles that had been there. An X tile could be designed to only slide into the lower left-hand corner of the board.
The goal is to use the technology to develop nanomachines that can be modified or repaired after they have already been built.
With this tile displacement process we discovered, it becomes possible to replace and upgrade multiple parts of engineered nanoscale machines to make them more efficient and sophisticated.


Ref: Philip Petersen, Grigory Tikhomirov, Lulu Qian. Information-based autonomous reconfiguration in systems of interacting DNA nanostructuresNature Communications, 2018; 9 (1) DOI: 10.1038/s41467-018-07805-7

Tuesday, 1 January 2019

E-bandage speeds wound healing in rats

A wound covered by an electric bandage on a rat's skin (top left) healed faster than a wound under a control bandage (right).
Credit: American Chemical Society

Skin has a remarkable ability to heal itself. But in some cases, chronic skin wounds include diabetic foot ulcers, venous ulcers and non-healing surgical wounds heal very slowly or not at all, putting a person at risk for chronic pain, infection and scarring. Doctors have tried various approaches to help chronic wounds heal, including bandaging, dressing, exposure to oxygen and growth-factor therapy, but they often show limited effectiveness. Now, researchers have developed a self-powered bandage that generates an electric field over an injury, dramatically reducing the healing time for skin wounds in rats. Weibo Cai, Xudong Wang and colleagues wanted to develop a flexible, self-powered bandage that could convert skin movements into a therapeutic electric field.

To power their electric bandage, or e-bandage, the researchers made a wearable nanogenerator by overlapping sheets of polytetrafluoroethylene (PTFE), copper foil and polyethylene terephthalate (PET). The nanogenerator converted skin movements, which occur during normal activity or even breathing, into small electrical pulses. This current flowed to two working electrodes that were placed on either side of the skin wound to produce a weak electric field. The team tested the device by placing it over wounds on rats' backs. Wounds covered by e-bandages closed within 3 days, compared with 12 days for a control bandage with no electric field. The researchers attribute the faster wound healing to enhanced fibroblast migration, proliferation and differentiation induced by the electric field.
Ref:  Yin Long, Hao Wei, Jun Li, Guang Yao, Bo Yu, Dalong Ni, Angela LF Gibson, Xiaoli Lan, Yadong Jiang, Weibo Cai, Xudong Wang. Effective Wound Healing Enabled by Discrete Alternative Electric Fields from Wearable NanogeneratorsACS Nano, 2018. 

Saturday, 29 December 2018

World’s first true blue roses could be coming soon!




By expressing bacterial genes, white rose petals can take on a blue hue (Image: American Chemical Society)



For centuries, gardeners have attempted to breed blue roses with no success. But now, thanks to modern biotechnology, the elusive blue rose may finally be attainable. Researchers have found a way to express pigment-producing enzymes from bacteria in the petals of a white rose, tinting the flowers blue.

Although blue roses do not exist in nature, florists can produce blue-hued flowers by placing cut roses in dye. Also, in a painstaking 20-year effort, biotechnologists made a "blue rose" through a combination of genetic engineering and selective breeding. However, the rose is more mauve-colored than blue. 

A completely different strategy presented in this study employs a dual expression plasmid containing bacterial idgS and sfp genes. The holo-IdgS, activated by Sfp from its apo-form, is a functional nonribosomal peptide synthetase that converts l-glutamine into the blue pigment indigoidine. Expression of these genes upon petal injection with agro-infiltration solution generates blue-hued rose flowers. We envision that implementing this proof-of-concept with obligatory modifications may have tremendous impact in floriculture to achieve a historic milestone in rose breeding.

Ref: Ankanahalli N. Nanjaraj Urs, Yiling Hu, Pengwei Li, Zhiguang Yuchi, Yihua Chen, Yan Zhang. Cloning and Expression of a Nonribosomal Peptide Synthetase to Generate Blue Rose. ACS Synthetic Biology, 2018; DOI: 10.1021/acssynbio.8b00187

Thursday, 19 April 2018

More than five glasses of alcoholic drink could shorten your life


According to new research from the University of Cambridge, regularly drinking more than the recommended UK guidelines for alcohol could take years off your life. The study compared the health and drinking habits of over 600,000 people in 19 countries worldwide and controlled for age, smoking, history of diabetes, level of education and occupation.
The upper safe limit of drinking was about five drinks per week (100g of pure alcohol, 12.5 units or just over five pints of 4% ABV beer or five 175ml glasses of 13% ABV wine). However, drinking above this limit was linked with lower life expectancy.
Alcohol consumption was associated with a higher risk of stroke, heart failure, fatal aortic aneurysms, fatal hypertensive disease and heart failure and there were no clear thresholds where drinking less did not have a benefit.

Cardiovascular disease may relate to alcohol's elevating effects on blood pressure and on factors related to elevated high-density lipoprotein cholesterol (HDL-C) (also known as 'good' cholesterol).  Alcohol consumption is associated with a slightly lower risk of non-fatal heart attacks but this must be balanced against the higher risk associated with other serious and potentially fatal cardiovascular diseases.

If you already drink alcohol, drinking less may help you live longer and lower your risk of several cardiovascular conditions.
1.      

   Ref. Angela M Wood et al. Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studiesThe Lancet, 2018; 391 (10129): 1513 DOI: 10.1016/S0140-6736(18)30134-X
     

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