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	<title>Multicellular Organisms Archives - InnoHEALTH magazine</title>
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		<title>Keys to Immortality &#8211; Telomerase, Stem Cells &#038; Gene Therapy</title>
		<link>https://innohealthmagazine.com/2019/well-being/telomerse-stem-cells-gene-therapy/</link>
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		<dc:creator><![CDATA[InnoHEALTH Magazine]]></dc:creator>
		<pubDate>Wed, 30 Oct 2019 11:27:11 +0000</pubDate>
				<category><![CDATA[Well Being]]></category>
		<category><![CDATA[abnormal somantic cells]]></category>
		<category><![CDATA[Adwaita]]></category>
		<category><![CDATA[Aldabra Giant Tortoise]]></category>
		<category><![CDATA[cancer cells]]></category>
		<category><![CDATA[chromosome]]></category>
		<category><![CDATA[death]]></category>
		<category><![CDATA[DNA]]></category>
		<category><![CDATA[eternal]]></category>
		<category><![CDATA[gene therapy]]></category>
		<category><![CDATA[generations]]></category>
		<category><![CDATA[germ cells]]></category>
		<category><![CDATA[human somantic cell]]></category>
		<category><![CDATA[immortal]]></category>
		<category><![CDATA[Life]]></category>
		<category><![CDATA[limitless replicative potential]]></category>
		<category><![CDATA[mortal]]></category>
		<category><![CDATA[Multicellular Organisms]]></category>
		<category><![CDATA[Mutation]]></category>
		<category><![CDATA[Physiological]]></category>
		<category><![CDATA[replication mechanism]]></category>
		<category><![CDATA[sickle cell disease]]></category>
		<category><![CDATA[stem cell]]></category>
		<category><![CDATA[Stem cell therapy]]></category>
		<category><![CDATA[technique]]></category>
		<category><![CDATA[telemere]]></category>
		<category><![CDATA[telomerase]]></category>
		<category><![CDATA[unicellular organisms]]></category>
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					<description><![CDATA[<p>We age and we die. Human is multicellular organism. In a nutshell, we can say – we age because our cells age. They don’t die of aging.</p>
<p>The post <a href="https://innohealthmagazine.com/2019/well-being/telomerse-stem-cells-gene-therapy/">Keys to Immortality &#8211; Telomerase, Stem Cells &amp; Gene Therapy</a> appeared first on <a href="https://innohealthmagazine.com">InnoHEALTH magazine</a>.</p>
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	<h2>Man is mortal! But his desire to be immortal is eternal.</h2>
<p style="text-align: justify !important;">There are many new possibilities that can make a human being nearly immortal, if not completely. Sounds impossible? Well, over the past few decades, medical science has made such progress that we at least discuss these possibilities. We already have immortals on Earth. Yes! But they are unicellular organisms. They don’t die of aging. These organisms divide into two, to keep their generations going. And they can do this limitless time. On the other hand, we grow up and every single second of our life we are marching towards death. We age and we die. Human is multicellular organism. In a nutshell, we can say – we age because our cells age. Normal human somatic cells do not have limitless replicative potential. Every normal human somatic cell divides 50-70 times (Hayflick limit or Hayflick phenomenon). Thus, when this limit is achieved, signs of aging and various diseases come into play. While the average life span of a normal human being is 80 years, some of the species can even live up to 200 years or more. Yes, a tortoise named Adwaita (species: Aldabra Giant Tortoise) lived more than 250 years. Don’t be surprised. I have seen this one alive. So, there must be something in our gene that basically controls the number of cell divisions we shall have and ultimately controls our life span. After years of research, scientists got the answer.</p>
<p><em><strong>Also Read: <a href="https://innohealthmagazine.comtrends/top-9-latest-healthcare-innovations/">Top 9 latest healthcare innovations</a></strong></em><br />
<strong>Telomeres</strong></p>
<p style="text-align: justify !important;">A telomere is a region of repetitive nucleotide sequences at each end of a chromosome, which protects the end of the chromosome from deterioration or from fusion with neighboring chromosomes. With each cell division, the telomere gets shortened because of normal DNA replication mechanism and after a certain number of divisions, a time comes when it is completely lost. That is the limit. Because if the cell divides again, it cannot preserve its genetic information completely and thus it is better not to divide than giving birth to faulty systems. Human germ cells are an exception in this case.</p>
<p><strong><em>Also Read: <a href="https://innohealthmagazine.comtrends/chewing-tobacco-storehouse-of-toxic-chemicals/">Chewing Tobacco – Storehouse of Toxic Chemicals</a></em></strong></p>
<p style="text-align: justify !important;">These cells contain an enzyme named ‘Telomerase’. Simply saying, this enzyme helps to expand the Telomere sequence and hence human germ cells achieve limitless replicative potential. Many scientists are working on this principle of the human germ cells. Their goal is to somehow introduce this property of germ cells into the somatic cells and achieve limitless replicative potential within physiological limits. Signs of aging and age-related degenerative diseases, as well as some chronic diseases, will be easier to handle then. But it’s not going to be so easy. This phrase <strong>‘within physiological limit’</strong> is very important. Because we already know some abnormal somatic cells which switch on the ‘telomerase’ gene and achieve this potential. Cancer cells! Yes, one of the deadly properties of cancer cells is they replicate infinite times and die only when the individual dies! Some of the cancer cells do activate telomerase enzyme to achieve that. It is the hardest hurdle they are facing in telomerase therapy.</p>
<p><strong><em>Also Read: <a href="https://innohealthmagazine.comtrends/iit-kharagpur-develops-diagnostic-tools-lungs-diseases/">IIT Kharagpur Develops Diagnostic Tools for Lung Diseases</a></em></strong></p>
<p style="text-align: justify !important;">If scientists can overcome this hurdle, it will open new doors in medical science. If doctors can control this telomerase activity, they will be able to regenerate damaged tissue or even the entire organ from a single cell and thus one can be nearly immortal. Imagine a patient with liver cirrhosis who will not undergo a liver transplant. Instead, under the controlled intervention of gene therapy, his liver will regrow! And no chance of graft rejection. Myocardial infraction, stroke, and many more complicated conditions will be easily cured. But this therapy needs a fair bit of research and a number of advancements to be used as a trial even. But for the time being, we have another technique that has gained a good response over the past few years.</p>
<p><strong><em>Also Read: <a href="https://innohealthmagazine.comtrends/apple-watch-prevent-skin-diseases/">Apple Watch Can Soon Prevent Skin Diseases</a></em></strong><br />
<strong>Stem Cell Therapy</strong></p>
<p style="text-align: justify !important;">The entire human body is made up of trillions of different types of cells. But interestingly they all came from a single cell. Embryonic Stem Cells (Pluripotent) are those cells that give rise to any kind of cell the human body possesses. It has been scientifically proven that if we amputate the finger of a growing embryo at the initial few weeks, it regenerates scarlessly. It means at that stage of life cells are capable of regeneration. Per recent advancements, the scientists are using this property and trying to regenerate a whole organ with these pluripotent stem cells. Again, let’s give the example of the same liver cirrhosis patient. If scientists achieve success in this therapy, doctors will be introducing the stem cells into the liver and it will regenerate and achieve its functionality again. This therapy has been tested in leukemia patients successfully. That gives us a ray of hope that in near future this technique might be used as a treatment of many diseases that seem to be incurable now.</p>
<p><strong><em>Also Read: <a href="https://innohealthmagazine.comresearch/can-millets-answer-indias-nutritional-problems/">Can Millets Be the Answer to India’s Nutritional Problems?</a></em></strong></p>
<p style="text-align: justify !important;">Another possibility can be <strong>Gene Therapy</strong>. As we grow old, our cells divide a number of times and in the course may get mutated. Mutations in genes can give rise to a number of deadly diseases like malignancies. Mutation can be a point mutation or a whole segment of the gene can be affected. These days scientists are able to replace the faulty portion of the gene with the normal one and that opens a whole lot of possibilities to treat genetic diseases. In case of congenital genetic abnormalities,they are basically combining two abovementioned therapies for the mankind.</p>
<p><strong><em>Also Read: <a href="https://innohealthmagazine.comnewscope/diabetes-digital-tools-unmet-needs/">Unmet Needs, Diabetes and Digital Tools</a></em></strong><br />
<strong>Stem Cell Therapy + Gene Therapy</strong></p>
<p style="text-align: justify !important;">As an example, in case of sickle cell disease – scientists isolate the pluripotent haematopoiesis stem cells and correct the genetic abnormality. Upon introduction to the body, these stem cells produce normal blood cells.</p>
<p style="text-align: justify !important;">All the techniques mentioned above are going to be the future of the medical science. These can definitely increase the life span as well as the quality of life. But these all techniques are at the initial stages and need to go through a number of trials to be accepted as TREATMENT. The way medical science is advancing, we can certainly expect it sooner.</p>
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	<h2>About the author</h2>
<p style="text-align: justify !important;"><em><strong>Mahan Shome</strong></em> is a young medico studying medicine abroad. In his leisure time, Mahan likes to read innovative scientific health articles. His dream is to be part of healthcare research that brings about advancement in medicine. He hails from Howrah, West Bengal.</p>
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<p>The post <a href="https://innohealthmagazine.com/2019/well-being/telomerse-stem-cells-gene-therapy/">Keys to Immortality &#8211; Telomerase, Stem Cells &amp; Gene Therapy</a> appeared first on <a href="https://innohealthmagazine.com">InnoHEALTH magazine</a>.</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">6602</post-id>	</item>
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		<title>Molecular mechanics controlling the circadian rhtythm</title>
		<link>https://innohealthmagazine.com/2018/persona/molecular-mechanism/</link>
					<comments>https://innohealthmagazine.com/2018/persona/molecular-mechanism/#respond</comments>
		
		<dc:creator><![CDATA[InnoHEALTH Magazine]]></dc:creator>
		<pubDate>Wed, 07 Feb 2018 07:26:27 +0000</pubDate>
				<category><![CDATA[Persona]]></category>
		<category><![CDATA[Astronomer Jean Jacques d'Ortous de Mairan]]></category>
		<category><![CDATA[Biological Clock]]></category>
		<category><![CDATA[Biological Rhythm]]></category>
		<category><![CDATA[Boston]]></category>
		<category><![CDATA[Brandeis University]]></category>
		<category><![CDATA[Cell Nucleus]]></category>
		<category><![CDATA[Ciradian Rhythm]]></category>
		<category><![CDATA[Circadianrhythm]]></category>
		<category><![CDATA[Clock Gene]]></category>
		<category><![CDATA[Cytoplasm]]></category>
		<category><![CDATA[DBT]]></category>
		<category><![CDATA[Dynamic Research]]></category>
		<category><![CDATA[Dynamic Trio]]></category>
		<category><![CDATA[External Environment]]></category>
		<category><![CDATA[Health and wellbeing]]></category>
		<category><![CDATA[Hormone Level]]></category>
		<category><![CDATA[Human Physiology]]></category>
		<category><![CDATA[Inner Clock]]></category>
		<category><![CDATA[Jeffrey C. Hall]]></category>
		<category><![CDATA[Jet lag]]></category>
		<category><![CDATA[Mechanistic Principles]]></category>
		<category><![CDATA[Metabolism]]></category>
		<category><![CDATA[Micheal Rosbash]]></category>
		<category><![CDATA[Micheal W. Young]]></category>
		<category><![CDATA[Mimosa Plant]]></category>
		<category><![CDATA[Mimosa Plants]]></category>
		<category><![CDATA[Molecular Components]]></category>
		<category><![CDATA[Molecular Mechanisms]]></category>
		<category><![CDATA[mRNA]]></category>
		<category><![CDATA[Multi-cellular organism]]></category>
		<category><![CDATA[Multicellular Organisms]]></category>
		<category><![CDATA[Nobel Prize Winner]]></category>
		<category><![CDATA[Noble Prize]]></category>
		<category><![CDATA[PER]]></category>
		<category><![CDATA[Physiology]]></category>
		<category><![CDATA[Rockefeller University]]></category>
		<category><![CDATA[Ronald Konopka]]></category>
		<category><![CDATA[Seymour Benzer]]></category>
		<category><![CDATA[TIM]]></category>
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					<description><![CDATA[<p>For many years we have known that living organisms, including humans, have an internal, biological clock that helps them anticipate and adapt to the regular rhythm of the day. Jeffrey C. Hall, Michael W. Young and Michael Rosbash 2017 Nobel Prize winners discovered molecular mechanism controlling the circadian rhythm</p>
<p>The post <a href="https://innohealthmagazine.com/2018/persona/molecular-mechanism/">Molecular mechanics controlling the circadian rhtythm</a> appeared first on <a href="https://innohealthmagazine.com">InnoHEALTH magazine</a>.</p>
]]></description>
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	<p style="text-align: justify !important;">Jeffrey C. Hall, Michael W. Young and Michael Rosbash 2017 Nobel Prize winners in Physiology or Medicine. Honored for their discoveries of molecular mechanisms controlling the circadian rhythm.</p>
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	<p style="text-align: justify !important;">Life on Earth is adapted to the rotation of our planet. For many years we have known that living organisms, including humans, have an internal, biological clock that helps them anticipate and adapt to the regular rhythm of the day. But how does this clock actually work? Jeffrey C. Hall, Michael Rosbash and Michael W. Young were able to peek inside our biological clock and elucidate its inner workings. Their discoveries explain how plants, animals and humans adapt their biological rhythm so that it is synchronized with the Earth’s revolutions.</p>
<p style="text-align: justify !important;">Using fruit flies as a model Honored for their discoveries of molecular mechanisms controlling the circadian rhythm organism, this year’s Nobel laureates isolated a gene that controls the normal daily biological rhythm. They showed that this gene encodes a protein that accumulates in the cell during the night, and is then degraded during the day. Subsequently, they identified additional protein components of this machinery, exposing the mechanism governing the self-sustaining clockwork inside the cell. We now recognize that biological clocks function by the same principles in cells of other multi-cellular organisms, including humans.</p>
<p style="text-align: justify !important;">With exquisite precision, our inner clock adapts our physiology to the dramatically different phases of the day. The clock regulates critical functions such as behavior, hormone levels, sleep, body temperature and metabolism. Our wellbeing is affected when there is a temporary mismatch between our external environment and this internal biological clock, for example when we travel across several time zones and experience “jet lag”. There are also indications that chronic misalignment between our lifestyle and the rhythm dictated by our inner timekeeper is associated with increased risk for various diseases.</p>
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	<p><span style="color: #0071b2;"><strong>Our inner clock</strong></span></p>
<p style="text-align: justify !important;">Most living organisms anticipate and adapt to daily changes in the environment. During the 18th century, the astronomer Jean Jacques d’Ortous de Mairan studied mimosa plants, and found that the leaves opened towards the sun during daytime and closed at dusk. He wondered what would happen if the plant was placed in constant darkness. He found that independent of daily sunlight the leaves continued to follow their normal daily oscillation (See figure). Plants seemed to have their own biological clock.</p>
<p style="text-align: justify !important;">Other researchers found that not only plants, but also animals and humans, have a biological clock that helps to prepare our physiology for the fluctuations of the day. This regular adaptation is referred to as the circadianrhythm, originating from the Latin words circa meaning “around” and diesmeaning “day”. But just how our internal circadian biological clock worked remained a mystery.</p>
<p><span style="color: #0071b2;"><strong>Identification of a clock gene</strong></span></p>
<p style="text-align: justify !important;">During the 1970’s, Seymour Benzer and his student Ronald Konopka asked whether it would be possible to identify genes that control the circadian rhythm in fruit flies. They demonstrated that mutations in an unknown gene disrupted the circadian clock of flies. They named this gene period. But how could this gene influence the circadian rhythm?</p>
<p style="text-align: justify !important;">This year’s Nobel Laureates, who were also studying fruit flies, aimed to discover how the clock actually works. In 1984, Jeffrey Hall and Michael Rosbash, working in close collaboration at Brandeis University in Boston, and Michael Young at the Rockefeller University in New York, succeeded in isolating the period gene. Jeffrey Hall and Michael Rosbash then went on to discover that PER, the protein encoded by period, accumulated during the night and was degraded during the day. Thus, PER protein levels oscillate over a 24-hour cycle, in synchrony with the circadian rhythm.</p>
<p><strong><span style="color: #0071b2;">A self-regulating clockwork mechanism</span></strong></p>
<p style="text-align: justify !important;">The next key goal was to understand how such circadian oscillations could be generated and sustained. Jeffrey Hall and Michael Rosbash hypothesized that the PER protein blocked the activity of the period gene. They reasoned that by an inhibitory feedback loop, PER protein could prevent its own synthesis and thereby regulate its own level in a continuous, cyclic rhythm.</p>
<p style="text-align: justify !important;">The model was tantalizing, but a few pieces of the puzzle were missing. To block the activity of the period gene, PER protein, which is produced in the cytoplasm, would have to reach the cell nucleus, where the genetic material is located. Jeffrey Hall and Michael Rosbash had shown that PER protein builds up in the nucleus during night, but how did it get there? In 1994 Michael Young discovered a second clock gene, timeless, encoding the TIM protein that was required for a normal circadian rhythm. In elegant work, he showed that when TIM bound to PER, the two proteins were able to enter the cell nucleus where they blocked period gene activity to close the inhibitory feedback loop.</p>
<p style="text-align: justify !important;">Such a regulatory feedback mechanism explained how this oscillation of cellular protein levels emerged, but questions lingered. What controlled the frequency of the oscillations? Michael Young identified yet another gene, double time, encoding the DBT protein that delayed the accumulation of the PER protein. This provided insight into how an oscillation is adjusted to more closely match a 24-hour cycle.</p>
<p style="text-align: justify !important;">The paradigm-shifting discoveries by the laureates established key mechanistic principles for the biological clock. During the following years other molecular components of the clockwork mechanism were elucidated, explaining its stability and function. For example, this year’s laureates identified additional proteins required for the activation of the period gene, as well as for the mechanism by which light can synchronize the clock.</p>
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	<p><span style="color: #0071b2;"><strong>Keeping time on our human physiology</strong></span></p>
<p style="text-align: justify !important;">The biological clock is involved in many aspects of our complex physiology. We now know that all multicellular organisms, including humans, utilize a similar mechanism to control circadian rhythms. A large proportion of our genes are regulated by the biological clock and, consequently, a carefully calibrated circadian rhythm circadian biology has developed into a vast and highly dynamic research field, with implications for our health and wellbeing.</p>
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	<p><strong>Read all the issues of InnoHEALTH magazine:</strong><br />
InnoHEALTH Volume 1 Issue 1 (July to September 2016) – <a href="https://goo.gl/iWAwN2">https://goo.gl/iWAwN2 </a><br />
InnoHEALTH Volume 1 Issue 2 (October to December 2016) – <a href="https://goo.gl/4GGMJz">https://goo.gl/4GGMJz </a><br />
InnoHEALTH Volume 2 Issue 1 (January to March 2017) – <a href="https://goo.gl/DEyKnw">https://goo.gl/DEyKnw </a><br />
InnoHEALTH Volume 2 Issue 2 (April to June 2017) – <a href="https://goo.gl/Nv3eev">https://goo.gl/Nv3eev</a><br />
InnoHEALTH Volume 2 Issue 3 (July to September 2017) – <a href="https://goo.gl/MCVjd6">https://goo.gl/MCVjd6</a><br />
InnoHEALTH Volume 2 Issue 4 (October to December 2017) – <a href="http://amzn.to/2B2UMLw">http://amzn.to/2B2UMLw</a><br />
InnoHEALTH Volume 3 Issue 1 (January to March 2018) – <a href="https://goo.gl/fksdQx">https://goo.gl/fksdQx</a></p>
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<p>The post <a href="https://innohealthmagazine.com/2018/persona/molecular-mechanism/">Molecular mechanics controlling the circadian rhtythm</a> appeared first on <a href="https://innohealthmagazine.com">InnoHEALTH magazine</a>.</p>
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