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Archive for the ‘Biological Networks, Gene Regulation and Evolution’ Category

Reporter: Prabodh Kandala, PhD

When it comes to the FOXP2 gene, humans have had most to shout about. Discoveries that mutations in this gene lead to speech defects and that the gene underwent changes around the time language evolved both implicate FOXP2 in the evolution of human language.

More recently, patterns of gene expression in birds, humans and rodents have suggested a wider role in the production of vocalisations. Yet numerous reports have established that FOXP2 shows very little genetic variation across even distantly related vertebrates – from reptiles to mammals — providing few extra clues as to the gene’s role.

A new study, undertaken by a joint of team of British and Chinese scientists, has found that this gene shows unparalleled variation in echolocating bats. The results, appearing in a study published in the online, open-access journal PLoS ONE on September 19, report that FOXP2 sequence differences among bat lineages correspond well to contrasting forms of echolocation.

Like speech, bat echolocation involves producing complex vocal signals via sophisticated coordination of the mouth and face. The involvement of FOXP2 in the evolution of echolocation adds weighty support to the theory that FOXP2 functions in the sensory-motor coordination of vocalisations.

Ref:

http://www.sciencedaily.com/releases/2007/09/070919073014.htm

 

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Reporter: Prabodh Kandala, PhD

Do special “human” genes provide the biological substrate for uniquely human traits, like language?

Genetic aberrations of the human FoxP2 gene impair speech production and comprehension, yet the relative contributions of FoxP2 to brain development and function are unknown.

Songbirds are a useful model to address this because, like human youngsters, they learn to vocalize by imitating the sounds of their elders.

Previously, Dr. Constance Sharff and colleagues found that, when young zebra finches learn to sing or when adult canaries change their song seasonally, FoxP2 is up-regulated in Area X, a brain region important for song learning.

Dr. Sebastian Haesler, Dr. Scharff, and colleagues experimentally reduce FoxP2 levels in Area X before zebra finches started to learn their song. They used a virus-mediated RNA interference for the first time in songbird brains.

The birds, with lowered levels of FoxP2, imitated their tutor’s song imprecisely and sang more variably than controls.

FoxP2 thus appears to be critical for proper song development.

These results suggest that humans and birds may employ similar molecular substrates for vocal learning, which can now be further analyzed in an experimental animal system.

Abstract:

The gene encoding the forkhead box transcription factor, FOXP2, is essential for developing the full articulatory power of human language. Mutations of FOXP2 cause developmental verbal dyspraxia (DVD), a speech and language disorder that compromises the fluent production of words and the correct use and comprehension of grammar. FOXP2 patients have structural and functional abnormalities in the striatum of the basal ganglia, which also express high levels of FOXP2. Since human speech and learned vocalizations in songbirds bear behavioral and neural parallels, songbirds provide a genuine model for investigating the basic principles of speech and its pathologies. In zebra finch Area X, a basal ganglia structure necessary for song learning, FoxP2 expression increases during the time when song learning occurs. Here, we used lentivirus-mediated RNA interference (RNAi) to reduce FoxP2 levels in Area X during song development. Knockdown of FoxP2 resulted in an incomplete and inaccurate imitation of tutor song. Inaccurate vocal imitation was already evident early during song ontogeny and persisted into adulthood. The acoustic structure and the duration of adult song syllables were abnormally variable, similar to word production in children with DVD. Our findings provide the first example of a functional gene analysis in songbirds and suggest that normal auditory-guided vocal motor learning requires FoxP2.

Ref:

1. http://www.sciencedaily.com/releases/2007/12/071204091933.htm

2. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2100148/

2.

 

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Reporter: Prabodh Kandala, PhD

Foxp2, a gene involved in speech and language, helps regulate the wiring of neurons in the brain, according to a study which will be published on July 7th in the open-access journal PLoS Genetics. The researchers identified this functional link by first identifying the major targets of Foxp2 in developing brain tissue and then analysing the function of relevant neurons.

Foxp2 codes for a regulatory protein that provides a window into unusual aspects of brain function. In 2001, scientists discovered that mutations of the human gene cause a rare form of speech and language disorder. The finding triggered a decade of intense research into the human gene and corresponding versions found in other species — for example, it has been shown to affect vocal imitation in songbirds, and learning of rapid movement sequences in mice.

In the PLoS Genetics study, the researchers, led by Dr. Sonja C. Vernes and Dr. Simon E. Fisher (The Wellcome Trust Centre for Human Genetics, University of Oxford), gained insights into the functions of Foxp2 within the developing brain by exploiting its role as a genetic dimmer switch, turning up or down the amount of product made by other genes. In their large-scale screening of embryonic brain tissue, they identified many novel targets regulated by Foxp2. Remarkably, many of these targets were known to be important for connectivity of the central nervous system. The team went on to show that changing Foxp2 levels in neurons impacted on the length and branching of neuronal projections, a key route for modulating the wiring of the developing brain.

“Studies like this are crucial for building bridges between genes and complex aspects of brain function” says Dr. Fisher, who is also director of a newly established Language and Genetics department at the Max Planck Institute for Psycholinguistics, The Netherlands. The research was carried out with mouse models, since they can be used to comprehensively analyse genetic networks in a way that remains difficult in the human brain. However, “the current study provides the most thorough characterisation of Foxp2 target pathways to date,” notes Dr. Fisher. “It offers a number of compelling new candidate genes that could be investigated in people with language problems.”

Abstract:

Forkhead-box protein P2 is a transcription factor that has been associated with intriguing aspects of cognitive function in humans, non-human mammals, and song-learning birds. Heterozygous mutations of the human FOXP2 gene cause a monogenic speech and language disorder. Reduced functional dosage of the mouse version (Foxp2) causes deficient cortico-striatal synaptic plasticity and impairs motor-skill learning. Moreover, the songbird orthologue appears critically important for vocal learning. Across diverse vertebrate species, this well-conserved transcription factor is highly expressed in the developing and adult central nervous system. Very little is known about the mechanisms regulated by Foxp2 during brain development. We used an integrated functional genomics strategy to robustly define Foxp2-dependent pathways, both direct and indirect targets, in the embryonic brain. Specifically, we performed genome-wide in vivo ChIP–chip screens for Foxp2-binding and thereby identified a set of 264 high-confidence neural targets under strict, empirically derived significance thresholds. The findings, coupled to expression profiling and in situ hybridization of brain tissue from wild-type and mutant mouse embryos, strongly highlighted gene networks linked to neurite development. We followed up our genomics data with functional experiments, showing that Foxp2 impacts on neurite outgrowth in primary neurons and in neuronal cell models. Our data indicate that Foxp2 modulates neuronal network formation, by directly and indirectly regulating mRNAs involved in the development and plasticity of neuronal connections.

Ref:

http://www.sciencedaily.com/releases/2011/07/110707173316.htm

http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1002145

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Reporter: Prabodh Kandala, PhD

Scientists of the German Mouse Clinic at Helmholtz Zentrum München have made a major contribution to understanding human language development. Using a comprehensive screening method, they studied a mouse model carrying a “humanized version” of a key gene associated with human language.

In the brains of the mice the researchers found alterations which may be closely linked to speech and language development. Their analyses comprise part of an international study led by the Leipzig Max Planck Institute for Evolutionary Anthropology. The findings have been published in the current issue of the journal Cell.

Scientists of the German Mouse Clinic at Helmholtz Zentrum München have generated and analyzed a mouse model in which parts of the human Foxp2 gene were introduced. Foxp2 is known to be a key gene for language. Since the human and chimpanzee lineages diverged, only minimal genetic alterations have occurred, even with reference to the mouse: The alterations, as scientists surmised, are closely associated with speech and language ability. However, proof on a functional level has been lacking until now.

The Helmholtz scientists in the German Mouse Clinic conduct comprehensive analyses to elucidate which organs are influenced by a gene – in this case the Foxp2 gene. “It is rare for a gene to have only one function,” explained Professor Martin Hrabé de Angelis, director of the German Mouse Clinic. That is why a comprehensive research approach like that of the German Mouse Clinic is so crucial – to ensure that relevant gene functions can be identified in the mouse phenotype.

The study of the Foxp2 mice was funded within the scope of the National Genome Research Network (NGFN). As with each mouse lineage studied in the German Mouse Clinic, the Helmholtz scientists analyzed the Foxp2 mice by screening for more than 300 parameters, including the ability to see and hear, bone density, important metabolic functions and a number of neurological functions. The mice carrying the humanized Foxp2 gene showed no physiological abnormalities. However, behavioral tests showed an altered exploratory behavior and reduced movement activity – both results point to altered brain functions. Further investigations carried out by the colleagues in Leipzig supported and confirmed the findings.

In a second step to further substantiate this hypothesis, the Helmholtz scientists analyzed the heterozygous knockout mouse model in which one of the normally two copies of the Foxp2 gene is missing. This loss leads to serious changes: The ability of the mice to hear and learn is diminished in comparison to their healthy littermates; they have more fat and less muscle, and they eat more and consume more energy. Moreover, they have altered blood parameters.

“We were able to show that the Foxp2 gene has significant influence on various organ systems,” Martin Hrabé de Angelis said. “Our research supports the hypothesis of our colleagues in Leipzig that specifically these alterations in the brain were the evolutionary step that gave humans the advantage of speech and language.” Furthermore, the involvement of the Hrabé de Angelis team in the Leipzig study demonstrates the usefulness of the German Mouse Clinic. Only through broad-based, comprehensive analysis can scientists recognize even unexpected effects of genetic defects and thus identify additional functions of known genes.

Abstract:

It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been positively selected during human evolution due to effects on aspects of speech and language. Here, we introduce these substitutions into the endogenous Foxp2 gene of mice. Although these mice are generally healthy, they have qualitatively different ultrasonic vocalizations, decreased exploratory behavior and decreased dopamine concentrations in the brain suggesting that the humanized Foxp2 allele affects basal ganglia. In the striatum, a part of the basal ganglia affected in humans with a speech deficit due to a nonfunctional FOXP2allele, we find that medium spiny neurons have increased dendrite lengths and increased synaptic plasticity. Since mice carrying one nonfunctional Foxp2 allele show opposite effects, this suggests that alterations in cortico-basal ganglia circuits might have been important for the evolution of speech and language in humans.

Ref:

http://www.sciencedaily.com/releases/2012/08/120810193755.htm

http://www.cell.com/retrieve/pii/S009286740900378X

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Reporter: Prabodh Kandala, PhD

If humans are genetically related to chimps, why did our brains develop the innate ability for language and speech while theirs did not?

Part of the answer to this mystery lies in a gene called FOXP2. When mutated, FOXP2 can disrupt speech and language in humans. Now, a UCLA/Emory study reveals major differences between how the human and chimp versions of FOXP2 work, perhaps explaining why language is unique to humans.

The findings from this study provide insight into the evolution of the human brain and may point to possible drug targets for human disorders characterized by speech disruption, such as autism and schizophrenia.

Earlier research suggests that the amino-acid composition of human FOXP2 changed rapidly around the same time that language emerged in modern humans. This is the first study to examine the effect of these amino-acid substitutions in FOXP2 in human cells.

We showed that the human and chimp versions of FOXP2 not only look different but function differently too. These findings may shed light on why human brains are born with the circuitry for speech and language and chimp brains are not.

FOXP2 switches other genes on and off. Geschwind’s lab scoured the genome to determine which genes are targeted by human FOXP2. The team used a combination of human cells, human tissue and post-mortem brain tissue from chimps that died of natural causes.

The chimp brain dissections were performed in the laboratory of coauthor Todd Preuss, associate research professor of neuroscience at Emory University’s Yerkes National Primate Research Center.

The scientists focused on gene expression — the process by which a gene’s DNA sequence is converted into cellular proteins.

To their surprise, the researchers discovered that the human and chimp forms of FOXP2 produce different effects on gene targets in the human cell lines.

This study found that a significant number of the newly identified targets are expressed differently in human and chimpanzee brains. This suggests that FOXP2 drives these genes to behave differently in the two species.

The research demonstrates that mutations believed to be important to FOXP2’s evolution in humans change how the gene functions, resulting in different gene targets being switched on or off in human and chimp brains.

Genetic changes between the human and chimp species hold the clues for how our brains developed their capacity for language. By pinpointing the genes influenced by FOXP2, this interesting study shows a new set of tools for studying how human speech could be regulated at the molecular level.

The discovery will provide insight into the evolution of humans’ ability to learn through the use of higher cognitive skills, such as perception, intuition and reasoning.

This study demonstrates how critical chimps and macaques are for studying humans. They open a window into understanding how we evolved into who we are today.

Because speech problems are common to both autism and schizophrenia, the new molecular pathways will also shed light on how these disorders disturb the brain’s ability to process language.

Ref:

http://www.sciencedaily.com/releases/2009/11/091111130942.htm

 

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Reporter: Prabodh Kandala, PhD

Singing mice (scotinomys teguina) are not your average lab rats. Their fur is tawny brown instead of the common white albino strain; they hail from the tropical cloud forests in the mountains of Costa Rica; and, as their name hints, they use song to communicate.

University of Texas at Austin researcher Steven Phelps is examining these unconventional rodents to gain insights into the genes that contribute to the unique singing behavior — information that could help scientists understand and identify genes that affect language in humans.

“We can choose any number of traits to study but we try and choose traits that are not only interesting for their own sake but also have some biomedical relevance,” said Phelps. “We take advantage of the unique property of the species.”

The song of the singing mouse song is a rapid-fire string of high-pitched chirps called trills used mostly used by males in dominance displays and to attract mates. Up to 20 chirps are squeaked out per second, sounding similar to birdsong to untrained ears. But unlike birds, the mice generally stick to a song made up of only a single note.

“They sound kind of soft to human ears, but if you slow them down by about three-fold they are pretty dramatic,” said Phelps.

Most rodents make vocalizations at a frequency much too high for humans to hear. But other rodents typically don’t vocalize to the extent of singing mice, which use the song to communicate over large distances in the wild, said Andreas George, a graduate student working in Phelps’ lab.

Within the last year Phelps research on the behavior of the mouse has appeared in the journals Hormones and Behaviorand Animal Behavior. But one of his newest research projects is looking deeper: examining the genetic components that influence song expression. Center stage is a special gene called FOXP2.

“FOXP2 is famous because it’s the only gene that’s been implicated in human speech disorders specifically,” said Phelps.

Having at least one mutated copy of the gene has been associated with a host of language problems in humans, from difficulty understanding grammar to an inability to make the precise mouth movements needed to speak a clear sentence.

The FOXP2 gene is remarkably similar overall between singing mice, lab mice and humans, said Phelps. To find parts of the gene that may contribute to the singing mouse’s songs, Phelps is searching for sequences unique to the singing mouse and testing them for evidence of natural selection, which weeds out mutations with no likely observable effect from those that are likely to contribute to singing behavior.

“Those two things go a long way,” said Phelps, ” And when you look at the intersection of those two things they give us a really good set of candidate regions for what might be causing species differences.”

The Molecular Connection

Most genetic mutations don’t cause serious problems. They are often a part of the genome that is not expressed, still make a functional product, or are simply drowned out by the amount of genes and gene products that are working correctly.

FOXP2 mutations, on the other hand, can have significant effects on speech because of the gene’s role as a transcription factor — a gene product that helps control the expression of other genes.

This means a mutation in the FOXP2 gene can start a chain of events that can lead to reduced expression, or possibly even no expression, of a number of other genes.

Phelps and his team are figuring out what activates FOXP2 expression and the genes that are expressed after its activation by playing singing mice recording of songs from their own species and neighboring species and observing the gene expression patterns.

“We found that when an animal hears a song from the same species, these neurons that carry FOXP2 become activated. So we think that FOXP2 may play a role in integrating that information,” said Lauren O’Connell, a post-doctoral researcher in the Phelps lab.

Learning what activates FOXP2 and what genes are activated by it could provide clues into how outside stimuli affects gene expression and what genes are important in the understanding and integration of information, said Phelps.

“We ask two things, whether there are sequence changes in the DNA that are associated with the elaboration of the song and whether particular elements seem to be interacting with FOXP2 more,” said Phelps. “That gives us leads into what role FOXP2 might play into the elaboration of vocalization.”

Big Data Mining

Phelps’ uses next-generation sequencing to decipher how FOXP2 interacts with DNA to regulate the function of other genes. The process involves reading tiny fragments of overlapping DNA so that the entire sequence can be deduced. It is a procedure that generates massive amount of data that only the processing power of a supercomputer can handle, said O’Connell.

“You need TACC to do it,” said O’Connell, referring to the Texas Advanced Computing Center, which houses the supercomputers the lab uses. “The more data you have, the more memory it requires, so a lot of the data we can only process on Lonestar’s high memory nodes.”

Lonestar and Ranger are the names of the two supercomputers that the Phelps lab uses to crunch their data, with Ranger running programs in two hours that used to take the lab three days to run on their desktop. Both computers are among the top 100 supercomputers in the world.

Future Applications

At the most basic level, Phelps’ research is asking questions about the biology and behavior of an exotic rodent. But finding out more about the link between FOXP2 and the song of the signing mouse could bring a better understanding into how the gene may contribute to language deficits in people, especially those with autism, said Phelps.

“When people do genome wide association studies in humans the genetic variation tends to occur in huge blocks. So if you get some DNA sequence that predicts a phenotype, like risk for autism, it’s very hard to know what aspect in this very long stretch of DNA is actually important for that,” said Phelps.

By identifying the sequences of DNA that interact with FOXP2 and other associated genes that are most vital to gene function, researchers in the future might be able to narrow down the “huge blocks” where a possible causal sequence is located into smaller pieces. In other words, reducing the size of the metaphorical haystack to a size where finding the needle is a much simpler task.

While a singing mouse may seem like a strange place to look to study the impact of genetics on language, O’Connell says that the advent of gene sequencing technology is allowing a whole menagerie of animals to be used for research that could later be applied to humans.

“I use TACC to sequence a lot of different animals: birds and fish and frogs and mammals and beetles,” said O’Connell, mentioning the other organisms she studies outside of the Phelps lab. “Each of these model systems has something unique to contribute that teaches us about biology that is still applicable to humans.”

Abstracts:

1. Androgens are an important class of steroid hormones involved in modulating the expression and evolution of male secondary sex characters. Vocalizations used in the context of aggression and mate attraction are among the most elaborate and diverse androgen-dependent animal displays as reflected in a rich tradition of studies on bird song and anuran calls. Male Alston’s singing mice (Scotinomys teguina) commonly emit trilled songs that appear to function in male–male aggression. In this study, we experimentally manipulated androgens in singing mice to assess their role in modulating aggression and song effort. Testosterone- and DHT-treated animals retained aggressive and song attributes similarly. However, castrated mice administered empty implants showed more subordinate behavior and sang fewer songs that were shorter, lower in power, higher in frequency, and less stereotyped. The extensive effects of androgens on a suite of phenotypes highlight their role in linking gonadal status with decisions about investment in reproductive behaviors.

2.

Vocalizations used in aggressive and mating contexts often convey reliable information about signaller condition when physical or physiological limitations constrain signal expression. In vertebrates, androgens modulate the expression of vocal signals and provide a proximate link between male condition and signal form. In many songbirds, assessment of males is based on production of trills that are constrained by a performance trade-off between how fast notes are repeated and the frequency bandwidth of each note. In this study, we first recorded trills of male Neotropical singing mice (Scotinomys) to examine whether they show a similar performance trade-off, and then manipulated androgen levels to assess their role in modulating vocal performance. Lastly, we broadcast experimentally manipulated trills to females to determine whether they preferred versions resembling those of androgen-treated males. Singing mice showed a vocal performance trade-off similar to that of birds. Males treated with androgens maintained vocal performance, but castrated mice that were administered empty implants produced trills with lower performance. Females approached high-performance trills more rapidly and spent more time near corresponding speakers. Together, our results demonstrate that androgens modulate the production of physically challenging vocalizations, and the resulting signal variation influences female receiver response.

Ref:

1. http://www.sciencedaily.com/releases/2012/08/120810193755.htm

2. http://www.sciencedirect.com/science/article/pii/S0018506X10002746

3. http://www.sciencedirect.com/science/article/pii/S0003347211001795

 

 

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Curator/Author: Aviral Vatsa PhD, MBBS

Nitric oxide is one of the smallest molecules involved in physiological functions in the body. It is a diatom and thus seeks formation of chemical bonds with its targets rather than structure-function configuration of say protein receptors. Nitric oxide can exert its effects principally by two ways:

  • Direct
  • Indirect

Direct actions, as the name suggests, result from direct chemical interaction of NO with its targets e.g. with metal complexes, radical species. These actions occur at relatively low NO concentrations (<200 nM)

Indirect actions result from the effects of reactive nitrogen species (RNS) such as NO2 and N2O3. These reactive species are formed by the interaction of NO with superoxide or molecular oxygen. RNS are generally formed at relatively high NO concentrations (>400 nM)

Credits: Nitric Oxide: Biology and Pathobiology By Louis J. Ignarro

Credits: Nitric Oxide: Biology and Pathobiology By Louis J. Ignarro

Although it can be tempting for scientists to believe that RNS will always have deleterious effects and NO will have anabolic effects, this is not entirely true as certain RNS mediated actions mediate important signalling steps e.g. thiol oxidation and nitrosation of proteins mediate cell proliferation and survival, and apoptosis respectively. As depicted in the figure above, NO concentration determines the action it exerts on different proteins. This is highlighted in the following examples from different studies:

  • Cells subjected to NO concentration between 10-30 nM were associated with cGMP dependent phosphorylation of ERK
  • Cells subjected to NO concentration between 30-60 nM were associated with Akt phosphorylation
  • Concentration nearing 100 nM resulted in stabilisation of hypoxia inducible factor-1
  • At nearly 400 nM NO, p53 can be modulated
  • >1μM NO, it nhibits mitochondrial respiration

Besides the concentration, duration of NO exposure also determines how proteins respond to NO. Hence proteins can be ‘immediate’ responders or ‘delayed’ responders. The response can be either ‘transient’ (short lived) or ‘sustained’ (prolonged). Different proteins fall into these different categories. These are not rigid categories rather a functional ‘classification’.

Endogenously generated NO concentration ranges from 2 nM as in endothelial cell to >1 μM in a fully activated macrophage. This wide range, along with the unique chemical reactivity of NO offers immense versatility to the physiological effects that it can exert in different cellular milieu in the body.

In addition to the concentration-dependent effects, other factors that determine the local cellular/tissue milieu add to the complexities involved with signal transduction undertaken by NO. These factors are

  • rate of NO production
  • diffusion distance
  • rates of consumption
  • reactivity of RNS with molecular targets.

These kinetic determinants play vital role in physiological functions and disease states.

Although it is not possible to detail the modes of modulation of biological functions by NO in a short post, but I hope the post gives a taste of the intricacies involved with NO functions and that there are various parameters that determine the exact role of NO in a biological milieu.

Sources

http://www.pnas.org/content/101/24/8894.short

http://onlinelibrary.wiley.com/doi/10.1002/ijc.22336/full

http://cancerres.aacrjournals.org/content/67/1/289.short

http://www.sciencedirect.com/science/article/pii/S0005272806000417

http://goo.gl/eVXFh

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Reporter: Aviral Vatsa PhD, MBBS

A new study in JBMR highlights a novel glucocorticoid receptor modulator Compound A (CpdA) with the potential for an improved risk/benefit profile. They tested the effects of CpdA on bone in a mouse model of GC‐induced bone loss.

This study underlines the bone‐sparing potential of CpdA and suggests that by preventing increases in the RANKL/OPG ratio or DKK‐1 in osteoblast lineage cells, GC‐induced bone loss may be ameliorated. © 2012 American Society for Bone and Mineral Research.

RESULTS

PRED reduced the total and trabecular bone density in the femur by 9% and 24% and in the spine by 11% and 20%, respectively, whereas CpdA did not influence these parameters. Histomorphometry confirmed these results and further showed that the mineral apposition rate was decreased by PRED whereas the number of osteoclasts was increased. Decreased bone formation was paralleled by a decline in serum P1NP, reduced skeletal expression of osteoblast markers, and increased serum levels of the osteoblast inhibitor dickkopf‐1 (DKK‐1). In addition, serum CTX‐1 and the skeletal RANKL/OPG ratio were increased by PRED. None of these effects were observed with CpdA. Consistent with the in vivo data, CpdA did not increase the RANKL/OPG ratio in MLO‐Y4 cells. Finally, CpdA also failed to transactivate DKK‐1 expression in bone tissue, BMSCs and osteocytes.

METHODS

Bone loss was induced in FVB/N mice by implanting slow‐release pellets containing either vehicle, prednisolone (PRED) (3.5 mg), or CpdA (3.5 mg). After 4 weeks, mice were killed to examine the effects on the skeleton using quantitative computed tomography, bone histomorphometry, serum markers of bone turnover, and gene expression analysis. To assess the underlying mechanisms, in vitro studies were performed with human bone marrow stromal cells (BMSCs) and murine osteocyte‐like cells (MLO‐Y4 cells).

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Reporter: Aviral Vatsa MBBS PHD

Abstract

Wnt signaling is essential for osteogenesis and also functions as an adipogenic switch, but it is not known if interrupting wnt signaling via knockout of β‐catenin from osteoblasts would cause bone marrow adiposity. In this study the authors determined whether postnatal deletion of β‐catenin in preosteoblasts, through conditional cre expression driven by the osterix promoter, causes bone marrow adiposity. Postnatal disruption of β‐catenin in the preosteoblasts led to extensive bone marrow adiposity and low bone mass in adult mice. In cultured bone marrow‐derived cells isolated from the knockout mice, adipogenic differentiation was dramatically increased, whereas osteogenic differentiation was significantly decreased. As myoblasts, in the absence of wnt/β‐catenin signaling, can be reprogrammed into the adipocyte lineage, we sought to determine whether the increased adipogenesis we observed partly resulted from a cell‐fate shift of preosteoblasts that had to express osterix, (lineage‐committed early osteoblasts), from the osteoblastic to the adipocyte lineage. Using lineage tracing both in vivo and in vitro we demonstrated that the loss of β‐catenin from preosteoblasts caused a cell‐fate shift of these cells from osteoblasts to adipocytes, a shift that may at least partly contribute to the bone marrow adiposity and low bone mass in the knockout mice. These novel findings indicate that wnt/β‐catenin signaling exerts control over the fate of lineage‐committed early osteoblasts, with respect to their differentiation into osteoblastic vs. adipocytic populations in bone, and thus offers potential insight into the origin of bone marrow adiposity. © 2012 American Society for Bone and Mineral Research.

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Author/Curator: Aviral Vatsa PhD, MBBS

Nitric oxide (NO) is of extreme biological interest due to its wide range of physiological functions in almost all the human systems. For long it has been of vital interest to chemists, environmental scientists, metallurgists and other domains. It is only recently that the world of biology has discovered the ubiquitous presence of this small molecule in human body and the scientific exploration of its effects has grown ever since. It was only in 1980s that three different groups demonstrated that NO is indeed produced by mammalian cells and that NO has specific biological roles in the human body. These studies highlighted the role of NO in cardiovascular, nervous and immune systems. In cardiovascular system NO was shown to cause relaxation of vascular smooth muscle cells causing vasodilatation, in nervous system NO acts as a signalling molecule and in immune system it is used against pathogens by the phagocytosis cells. These pioneering studies opened the path of investigation of role of NO in biology. In 1998, three scientists, Robert F Furchgott, Louis J Ignarro, and Ferid Murad, were awarded Nobel Prize for their discoveries concerning ‘nitric oxide as a signalling molecule’.

Since then hundreds and thousands of publications have appeared in the scientific literature. These studies have attributed a wide range of biological functions to NO. A few important examples are:

  • toxic free radical causing injury to proteins, lipids and DNA
  • mediator of synaptic plasticity
  • intercellular neuronal signalling molecule
  • pro and anti inflammatory molecule
  • role in cell degeneration and ischaemia-reperfusion injury
  • role in atherosclerosis and inherited motor disorders
  • role in bone remodelling

The above list is by no means exhaustive, but it gives an idea about the ubiquitous involvement of NO in human systems.

Since NO has been implicated in various disease states, it has also been a prime target to achieve therapeutic benefits. Efforts are ongoing to investigate the therapeutic potential of NO in cardiovascular diseases, sepsis and shock, respiratory ailments, neuronal disease and bone conditions…just to name a few.

Although a lot of progress has happened in our understanding of this small molecule since its discovery, but still there are many challenges that the researchers face today while investigating NO. These are primarily because NO is metabolised very quickly (<5 sec) and it can difuse freely across cellular membranes owing to its chemical structure. This is the precise reason why it can act as a potent signaling molecule across systems in the first place. New techniques are appearing to delineate the role of NO at sub-cellular level and have promising potential to aid NO research in the future.

In the future posts on this topic I will strive to cover different aspects of NO physiology and its role in various disease conditions, techniques for NO detection, signaling mechanism etc.

Sources:

1. The nature of endothelium-derived vascular relaxant factor

Nature 308, 645 – 647 (12 April 1984); doi:10.1038/308645a0

T. M. Griffith, D. H. Edwards, M. J. Lewis, A. C. Newby & A. H. Henderson

2. Nitric oxide: physiology, pathophysiology, and pharmacology.

Pharmacological Rev June 1991 43:109-142

S Moncada, R M Palmer, and E A Higgs

3. Introduction to EDRF research.

J Cardiovasc Pharmacol.1993;22 Suppl 7:S1-2.

Furchgott RF

4. http://www.nobelprize.org/nobel_prizes/medicine/laureates/1998/illpres/

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