The positive effect of photobiomodulation in wound healing has previously been reported, however there is a considerable lack of knowledge regarding the molecular mechanisms involved, and no consensus on light parameters. Cytochrome c oxidase (CCO) is established as the main photoreceptor in cells, but light also induces nitric oxide (NO), production of reactive oxygen species (ROS) and activation of ion channels. Emerging new molecular targets include the GPCRs opsins (OPNs) and the circadian clock transcription factors, cryptochromes (CRYs). Localisation of OPN1-SW, OPN3, OPN5, CRY1 and CRY2 was seen in female facial and abdominal human skin. Furthermore, expression of these photoreceptors was retained in primary epidermal keratinocytes and dermal fibroblasts in culture; both cell types expressed OPN1-SW, OPN3, CRY1 and CRY2, at the mRNA and protein level. OPN2 was only expressed in cultured dermal fibroblasts, while in line with in situ expression, OPN5 was only expressed in cultured keratinocytes. The photoreceptor-expressing cultured epidermal keratinocytes demonstrated a dose- and wavelength- dependent response in both metabolic activity and cell migration in a scratch-wound assay. Specifically, low dose (2 J/cm2) blue light (447 nm) increased metabolic activity, but it did not impact keratinocyte migration. In contrast, high dose (30 J/cm2) blue light had no effect on metabolism, but inhibited migration of epidermal keratinocytes. Red light (655 nm) at 30 J/cm2 stimulated metabolic activity but did not modulate migration, while a higher dose of 60 J/cm2 had no effect on keratinocyte metabolic activity. In order to study OPN3 and CRY1 function, they were silenced in keratinocytes using siRNA; additionally 8 μM KL001 was used to stabilize CRY1. KL001 inhibited migration, and induced KRT1 and KRT10, an effect which was abrogated by knockdown of OPN3. Interestingly, knockdown of OPN3 upregulated CRY1 expression, while KL001 upregulated OPN3 expression, indicating a regulation by OPN3 of the molecular epidermal clock. Low levels of blue light increased early differentiation of epidermal keratinocytes, which was mediated by OPN3 and circadian clock mechanisms. However, low levels of blue light decreased keratinocyte DNA synthesis, which was mediated by circadian clock independently of OPN3. Translation of parameters ex vivo showed increasing re-epithelialisation and induction of OPN3 and CRY1 expression following exposure to 2 J/cm2 of blue light; however high doses of blue light inhibited re-epithelialisation. Red light, also increased re-epithelialisation, but had no effect on OPN3 or CRY1 expression. In conclusion, photoreceptors are expressed in human skin and they mediate DNA synthesis, migration and differentiation of epidermal keratinocytes. Furthermore, low dose of blue light interacts with OPN3 to induce epidermal differentiation, through the regulation of the circadian clock. A better understanding of the molecular mechanisms behind the photobiomodulation response in vitro will help to develop light based therapies for human wound healing. Interestingly, selected light parameters translated to human ex vivo skin showed a beneficial effect of low doses of blue (2 J/cm2) and red (30 J/cm2) light in re-epithelialisation. / Marie Curie ... the CLaSSiC project

yes / Photobiomodulation is reported to positively influence hair regrowth, wound healing, skin rejuvenation, and psoriasis. Despite rapid translation of this science to commercial therapeutic solutions, significant gaps in our understanding of the underlying processes remain. The aim of this review was to seek greater clarity and rationality specifically for the selection of optical parameters for studies on hair regrowth and wound healing. Our investigation of 90 reports published between 1985-2015 revealed major inconsistencies in optical parameters selected for clinical applications. Moreover, poorly understood photoreceptors expressed in skin such as cytochrome c oxidase, cryptochromes, opsins, may trigger different molecular mechanisms. All this could explain the plethora of reported physiological effects of light. To derive parameters for optimal clinical efficacy of photobiomodulation, we recommend a more rational approach, underpinning clinical studies with research of molecular targets and pathways using well-defined biological model systems enabling easy translation of optical parameters from in vitro to in vivo. Furthermore, special attention needs to be paid when conducting studies for hair regrowth, aiming for double-blind, placebo-controlled randomized clinical trials as the gold standard for quantifying hair growth. / European Marie-Curie Actions Programme, Grant agreement no.: 607886

Via la photosynthèse et la photomorphogenèse, la lumière contrôle fortement la ramification. Le rosier (Rosa hybrida L.) présente par exemple une inhibition complète du débourrement à l’obscurité. Mieux comprendre le mode d’action de la lumière offrira des possibilités nouvelles à l’horticulture. Peu de choses sont connues sur la signalisation de la lumière au cours du débourrement. Notamment, les rôles de chacun des photorécepteurs et des cytokinines (CK), hormones promotrices du débourrement, dans la transduction du signal lumineux n’ont pas été examinés. Dans ce travail, des apports exogènes et des dosages de CK à l’obscurité montrent que le photocontrôle du débourrement passe par la photorégulation des CK. La lumière contrôle la néosynthèse et le transport des CK depuis l’entre-nœud vers le bourgeon, et inhibe leur dégradation. Les CK néoformées initient le débourrement car elles régulent un ensemble de gènes majeurs du débourrement (signalisation des strigolactones, métabolisme et transport de l’auxine et des sucres, division et expansion cellulaires). Afin d’identifier les photorécepteurs impliqués dans ce processus, des études ont été menées chez le pois (Pisum sativum L.). Il en ressort que le profil de débourrement chez le pois est sous photocontrôle : basitone à la lumière, ce profil devient acrotone à l’obscurité ou suite aux simples et doubles mutations de phyA, phyB et cry1. Ces trois photorécepteurs jouent donc un rôle primordial sur les corrélations inhibitrices entre bourgeons. Des apports de CK permettent de restaurer le profil basitone du sauvage chez le mutant phyB, ce qui suggère que la signalisation de la lumière vers les CK passe par phyB. / Through photosynthesis and photomorphogenesis, light highly controls plant branching. Roses (Rosa hybrida L.) exhibit for example a strong inhibition of bud outgrowth under darkness. Better understanding the action of light in branching will give new opportunities to horticulturists. Yet, little is known about the light signalling pathway during bud outgrowth. In particular, the involvements of each photoreceptor and of cytokinins (CK), plant hormones acting as promoters of bud outgrowth, in the transduction of the light signal during bud outgrowth have not been assessed. In this work, exogenous applications and quantification of CK under darkness show that the photocontrol of bud outgrowth goes through the photo-regulation of CK. Light controls CK neo-synthesis and transport from the internode toward the bud, and inhibits their degradation. The neo-synthesised CK initiate bud outgrowth by regulating a set of major genes involved in bud outgrowth (strigolactones signalling, metabolisms and transports of auxin and of sugar, cell division and expansion). In order to identify the photoreceptors that are involved in this process, we studied pea (Pisum sativum L.) mutants. Our research indicate that the bud outgrowth profile along the stem is under photocontrol: being basitonic under white light, this profile becomes acrotonic under darkness or after mutations of phyA, phyB and cry1. These three photoreceptors thus play a major role in the control of the correlative inhibitions between buds. Since applications of CK allowed to restore the wild-type basitonic profile in the phyB mutant, this suggests that the light signalling pathway towards CK involves phyB.

Magnetoreception is the ability of some animals to use the weak magnetic field of the Earth for navigation over long-distance migrations. It is a well-known phenomenon, but its underlying biophysical mechanisms remain poorly understood. One proposal involves light-induced, magnetically sensitive chemical reactions occurring within cryptochrome proteins, rationalised via the radical pair mechanism (Chapter 1). The absence of evidence in support of this hypothesis is in part due to the lack of sufficiently sensitive techniques to measure magnetic field effects (MFEs) in biological samples. Cavity-enhanced detection, most commonly in the form of cavity ring-down spectroscopy (CRDS) or cavity-enhanced absorption spectroscopy (CEAS), is widely used in the gas phase to provide significant sensitivity gains over traditional single-pass measurements (Chapter 2). However, successful studies in the condensed phase are less prevalent due to the additional background losses inherent to the sample. This thesis reports on the application of broadband (i.e. monitoring > 100nm) variants of CRDS and CEAS to the study of MFEs on the radical recombination reactions of flavin-based systems in solution. The broadband CRDS (BBCRDS) instrument employed in Chapter 4 is able to monitor the spectral changes induced by magnetic fields with submicrosecond time resolution. However, the need to scan both the probe wavelength and time delay to construct time-resolved spectra leads to prohibitively long acquisition times, and hence exposure of sensitive samples to high numbers of photons. The broadband CEAS (BBCEAS) studies reported in Chapter 5 combine the high irradiance and spectral coverage of a supercontinuum radiation (SCR) source with a CCD detector to simultaneously acquire absorption spectra across the visible region (480–700nm). The CW nature of this technique precludes the possibility of following radical pair kinetics in real time. In an effort to combine the respective advantages of these two instruments, which individually have represented powerful advances in capability, a new cavity-enhanced technique is reported for the first time (Chapter 6). The result, optical cavity-enhanced transient absorption spectroscopy (OCTAS), is able to simultaneously monitor spectral evolution and associated MFEs on the microsecond timescale, with comparable sensitivity to the existing techniques. Magnetic responses in animal cryptochrome proteins have successfully been recorded using all three techniques, lending considerable weight to the hypothesis that these molecules are at the heart of the magnetic sense in animals.

Au cours de l’évolution, les plantes ont développé des mécanismes pour percevoir et s'adapter aux conditions de stress. Les formes actives de l'oxygène (FAO) sont des facteurs importants de l'état redox cellulaire et sont impliquées dans ces réponses. Le peroxyde d'hydrogène (H2O2), une FAO majeure des voies de signalisation oxydative, peut être produit rapidement dans la photorespiration. Chez Arabidopsis, le H2O2 produit dans la photorespiration est métabolisé notamment par la CATALASE2 (CAT2). Dans le contexte du mutant cat2 déficient pour cette catalase, les réponses au stress oxydatif induit par la production conditionnelle du H2O2 sont fortement dépendante de la photopériode. En particulier, la formation de lésions, accompagnée de réponses similaires à celles d' attaques pathogènes, sont spécifiques des conditions de culture en jours longs (JL). Ces effets ne sont pas observés en jours courts (JC) malgré un stress oxydant qui semble être aussi prononcé qu’en JL. Une approche transcriptomique globale a été utilisée pour explorer les patterns d’expression génique associées à ces effets. Elle a permis de mettre en évidence des interactions entre photopériode et H2O2 ou entre photopériode et CO2. En particulier, la majorité des gènes répondant à l' H2O2 dans le mutant cat2 sont induits lorsque les plantes sont cultivées en JC alors que un plus petit nombre sont induits par l’ H2O2 spécifiquement en JL. De façon générale, ces analyses ont mis en évidence des relations étroites entre les ressources carbonées, la lumière et l'état redox cellulaire dans les réponses aux changements environnementaux. Un gène induit par le H2O2 spécifiquement en JL, l’AZELAIC ACID INDUCED 1 (AZI1), a été sélectionné pour des analyses fonctionnelles à l’aide d’approches génétique, biochimique et transcriptomique. L’analyse de mutants cat2 azi1 a révélé que AZI1 ne semble pas jouer un rôle majeur dans les réponses des plantes à un stress oxydatif durable. Cependant, ce gène semble jouer un rôle important lorsque le stress oxydatif est déclenchée de façon abrupte par le transfert des plantes de conditions de culture en fort CO2 vers l'air ambiant. De plus, cette étude montre que la communication de feuille à feuille est impliquée dans la régulation de l'expansion de la mort cellulaire en réponse a l'H2O2 issue de la photorespiration. Dans la régulation de l'expansion des lésions, nous proposons que AZI1 agirait d'une part localement pour induire la mort cellulaire et d'autre en inhibant la mort cellulaire d'une façon systémique. Dans des fonds génétiques sauvage Col-0 ou mutant cat2, l’analyse comparative de mutants d'insertion ADN-T pour les principaux photochromes (phyA , phyB) et cryptochromes (cry1, cry2) a permis d'étudier les interactions entre les stress et les fonctions des photorécepteurs. Il est apparu que, la mutation des gènes PHY comme CRY conduit a une stimulation de l’accumulation de glutathion H2O2 dépendante. En revanche, dans le fond génétique cat2 contrairement à la perte des fonctions PHY, la mutation des gènes cry conduit a une modulation du profil transcritomique induit par l’ H2O2. De plus, un criblage de conditions de stress sur les simples mutants cry a révélé une plus forte sensibilité de ces génotypes au stress osmotique, a l’ H2O2 et au paraquat. Globalement, ces données indiquent que l’ensemble des photorécepteurs et plus particulièrement les cryptochromes peuvent jouer un rôle dans la réponse à l’ H2O2 intracellulaire suggérant ainsi l’existence d’un réseau complexe permettant l’intégration de conditions environnementales et la détermination de réponses appropriées au stress. / During evolution, plants have developed mechanisms to perceive and respond to stress conditions. Reactive oxygen species (ROS) are important components of cell redox state that have been implicated in these responses. H2O2, an important ROS molecule in oxidative signalling, can be produced rapidly in photorespiration. In Arabidopsis, photorespiratory H2O2 is notably metabolized by CATALASE2 (CAT2). Responses to oxidative stress induced conditionally by photorespiratory H2O2 in the catalase-deficient mutant, cat2, are highly determined by growth daylength. In particular, lesion formation, accompanied by induction of a range of pathogenesis responses, is specific to the long day (LD) photoperiod: these responses are not observed in short days (SD), even though oxidative stress seems to be as marked as in LD. A whole-genome transcriptomics approach was used to explore gene expression patterns underlying these effects, and identified interactions between daylength and H2O2 and between daylength and CO2. In particular, the majority of H2O2-responsive genes in cat2 were up-regulated more strongly in SD air, though a subset of H2O2-induced genes showed a LD-specific response. Overall, this analysis indicates close networking between carbon status, light, and redox state in environmental responses. The most strongly H2O2-induced gene in LD was azelaic acid induced 1 (AZI1) and this gene was chosen for functional analysis using a genetic, biochemical and transcript profiling approach. Analysis of cat2 azi1 mutants revealed that AZI1 does not seem to play an important role in the plant response to sustained, continuous oxidative stress, but is influential when oxidative stress is abruptly induced, in this case, by transferring plants from high CO2 to air. Moreover, this study provided evidence that leaf-to-leaf communication is involved in regulating cell death spread in response to photorespiratory H2O2. In the regulation of this lesion spread, it is proposed that AZI1 acts both locally to promote cell death as well as systemically to inhibit it. Using a comparative analysis of T-DNA insertion mutants for the major phytochromes (phyA, phyB) and cryptochromes (cry1, cry2) introduced into the Col-0 or cat2 background, interactions between stress and photoreceptor function were analyzed. A stimulatory effect of both phy and cry mutations on H2O2-triggered glutathione accumulation was apparent. In contrast to loss of PHY function, both cry mutations modulated daylength-dependent H2O2-triggered transcriptome profiles in cat2. In addition, stress screening of single cry mutants revealed effects on osmotic, H2O2 and paraquat sensitivity. Overall, these data show that both kinds of photoreceptor, but particularly cryptochromes, can play a role in the response to intracellular H2O2, suggesting that there is an intricate network allowing integration of environmental information to determine appropriate responses to stress.

Nature uses sunlight either as energy source or as information carrier. Photoreception is achieved by two groups of specialised proteins: photo-enzymes that catalyse photoreactions and photosensors that initiate physiological functions. In the present work mechanistic studies were conducted on one representative of each group by using site-directed mutagenesis as well as stationary and time-resolved spectroscopy. The photo-enzyme NADPH:Protochlorophyllide Oxidoreductase (POR) catalyses the light-dependent C17-C18 double bond reduction of protochlorophyllide, including a hydride and a proton transfer, to produce chlorophyllide, the immediate precursor of chlorophyll. POR provides a unique opportunity to study the hydride transfer mechanism in detail. Three distinct intermediates, prior to product formation, were observed that were interpreted as electron and proton-coupled electron transfer reactions from NADPH indicating a sequential hydride transfer mechanism. An active-site mutant, POR-C226S, yields distinct different intermediates compared to POR wild type but ends in the same chlorophyllide stereoisomer most likely due to an altered protochlorophyllide binding. This work provides the first direct observation of a stepwise hydride transfer mechanism in a biological system. Cryptochromes (CRY) are so far defined as flavoprotein blue-light photosensors that regulate the circadian clock throughout nature and are suggested as the candidate magnetoreceptor in animals. Animal CRY are subdivided into two classes of proteins: the light-responsive Type I (invertebrates) and the light-independent Type II (mainly vertebrates). The molecular basis of their different roles in the circadian clock is still unknown. Animal Type I CRY are suggested to undergo conformational changes - required for induction of subsequent signalling cascades - induced by the change in the FAD redox state due to light absorption. The study shows that in contrast to Type I animal Type II CRY do not bind tightly FAD as a cofactor due to the lack of structural features and therefore provide the molecular basis for their different biological roles ruling out a direct photomagnetoreceptor function. Further, detailed studies on a fruit fly (Dm)CRY reveal that it does not undergo a photocycle as FAD release and Trp decomposition were observed. Thus, it is suggested that light is a negative regulator of DmCRY stability linking the initial photochemistry to subsequent dark processes leading to signal transduction on a molecular level.

RESUME GENERAL<p><p>Contexte :une association entre exposition prolongée aux champs magnétiques (CM) d’extrêmement basses fréquences (ELF) et risque sanitaire a été établie pour la leucémie infantile (CM 50/60 Hz de l’électricité, RR = 2,0 pour ≥ 0,4 µT d‘intensité moyennée dans le temps) et est suggérée pour le décès par maladie d’Alzheimer (CM 50/60 Hz, CM 16,7 Hz des voies ferrées pour 21 µT d’intensité moyennée dans le temps) et pour certaines hémopathies chez l’adulte (CM 16,7 Hz). Ces associations restent inexpliquées à ce jour. Sur base d’observations animales (effets des CM ELF sur la sécrétion de mélatonine) d’une part, et de la sensibilité magnétique confirmée des cryptochromes (régulateurs des biorythmes) d’autre part, il a été suggéré que ces associations puissent être dues à une perturbation des biorythmes par les CM ELF. Selon les instances internationales, une intensité > 1 mT est requise pour l’existence d’effets biologiques. <p>Objectifs et méthode :sur base d’une revue exhaustive de la littérature et de modèles théoriques reconnus, le présent travail développe certains mécanismes possibles pour un effet perturbateur des biorythmes par les CM ELF. L’impact en santé publique de cette hypothèse est ensuite évalué. Enfin, des protocoles sont proposés pour sa mise à l’épreuve, tenant compte des mécanismes envisagés. <p>Résultats :la possibilité existe d’une interaction des oscillations ELF de l’intensité et/ou de l’orientation du CM (somme vectorielle du CM ELF et du CM terrestre ou CMT) avec les cryptochromes rétiniens. Chez l’animal magnétosensible (dont le rongeur), une perturbation des biorythmes pourrait être consécutive à un mécanisme non spécifique de perturbation sensorielle. Toute observation animale pourrait donc ne pas être extrapolable à l’Homme. Chez ce dernier, une perturbation des biorythmes pourrait être causée par les oscillations de l’intensité du CM (peut- être dès < 100 µT d’intensité de CM ELF). Une telle perturbation pourrait aussi être causée par les variations spatiales de l’intensité du CMT qui existent dans l’environnement résidentiel (proximité de structures métalliques). Par ailleurs, dans l’éventualité de l’existence, chez l’Homme également, d’une sensibilité directionnelle basée sur les cryptochromes rétiniens, les oscillations de l’orientation du CM pourraient alors aussi interférer avec ces cryptochromes (peut-être dès ≤ 10 µT). Dans l’hypothèse où une telle interférence affecte les biorythmes, seules pourraient alors être concernées les oscillations dont l’amplitude atteint plusieurs degrés d’angle. Un tel mécanisme ne pourrait donc s’appliquer à la relation entre CM ELF et leucémie infantile que dans l’éventualité où les intensités les plus élevées (+ 1 à 2 SD) de CM ELF y jouent un rôle. Au cas où l’hypothèse de la perturbation des biorythmes par les CM ELF se voyait confirmée, d’autres troubles de santé seraient alors concernés et d’autres sources de CM seraient en cause, tels les CM statiques d’intensité variable émis par les lignes de transport électrifié. Les paramètres d’exposition considérés devraient inclure l’orientation relative CM ELF/CMT, mais aussi l’intensité locale du CMT (facteur à la fois déterminant et confondant dans la présente hypothèse). L’expérimentation animale devrait investiguer l’expression des clock genes. L’expérimentation humaine devrait investiguer les biorythmes chez l’enfant. Et l’épidémiologie devrait investiguer l’incidence de troubles liés à une perturbation des biorythmes en relation avec l’exposition aux CM ELF ainsi qu’aux variations locales de l’intensité du CMT. <p>Conclusions :malgré les incertitudes persistantes quant aux fonctions précises des cryptochromes de la rétine humaine et quant à l’exactitude des modèles théoriques qui décrivent les interactions entre CM et cryptochromes, certains mécanismes paraissent possibles pour une interaction entre CM ELF et biorythmes. En l’absence persistante d’alternative valide pour l’explication de l’association entre CM ELF et leucémie infantile, l’hypothèse de la perturbation des biorythmes par ces CM paraît devoir être investiguée plus avant, mais en tenant compte des variations locales d’intensité du CMT. <p>Background: An association between prolonged exposure to extremely low frequency (ELF) magnetic fields (MF) and health risk has been established for childhood leukemia (50/60 Hz MF of electricity, RR = 2.0 for ≥ 0.4 µT of time-averaged intensity) and is suggested for death by Alzheimer's disease (50/60 Hz MF, 16.7 Hz MF of railways at 21 µT of time-averaged intensity) and for some hematologic malignancies in adults (16.7 Hz MF). These associations remain unexplained so far. Based on animal studies (effects of ELF MF on melatonin secretion) on the one hand, and on the confirmed magnetic sensitivity of cryptochromes (regulators of biorhythms) on the other hand, it has been suggested that these associations may be due to a disruption of biorhythms by ELF MF. From current data, however, biological effects seem only possible at > 1 mT of intensity.<p>Objectives and methods: on the basis of an exhaustive literature review and with use of recognized theoretical models, this paper develops some possible mechanisms for disruption of biorhythms by ELF MF. The public health impact of this hypothesis is then evaluated. Finally, protocols are proposed for the testing of it, with taking into account the proposed mechanisms.<p>Results: an interaction seems possible between ELF oscillations of the intensity and/or the orientation of the ambient MF (the vector sum of both the ELF MF and the geomagnetic field or GMF) with retinal cryptochromes. In magnetosensitive animals (including rodents), disruption of biorhythms may then be secondary to a non-specific mechanism of sensory disturbance. All animal observation could therefore not be extrapolated to humans. In the latter, on his turn, a disruption of biorhythms may be caused by the oscillations of the MF intensity (perhaps from <100 µT of ELF MF intensity). Such disruption could also be caused by spatial variations of the intensity of the GMF that exist in residential environment (near steel structures). Moreover, in case of the existence in humans (like in animals) of a directional sensitivity based on retinal cryptochromes, then the oscillations of the MF orientation also could interfere with these cryptochromes (perhaps from ≤ 10 µT). In the event that such interference affects biorhythms, only oscillations of several degrees of amplitude would then be concerned. As a consequence, such a mechanism could apply to the relation between ELF MF and childhood leukemia only in the event that the highest MF intensities (Mean + 1-2 SD) also play a role in that relation. In the event the hypothesis of disruption of biorhythms by ELF MF is confirmed, other health problems would be concerned and other kind of MF would be involved, such as the static MF of variable intensity that are emitted by the lines of electrified transport. The considered exposure parameters should include the relative orientation of ELF MF and GMF, but also the local intensity of GMF (both determining factor and confounder in this case). Animal experiments should investigate the expression of clock genes. Human experimentation should investigate biorhythms in children. And epidemiology should investigate the incidence of disorders related to disruption of biorhythms in relation to exposure to ELF MF as well as to local variations in the intensity of the GMF.<p>Conclusions: Despite the persisting uncertainties about the precise functions of retinal cryptochrome as well as about the accuracy of the theoretical models that describe the interactions between MF and cryptochromes, some mechanisms seem possible for an interaction between ELF MF and biorhythms. In the persisting absence of valid alternative explanation for the association between childhood leukemia and ELF MF, the hypothesis of biorhythm disturbance by ELF MF deserves further investigation, however with taking into account local intensity variations of the GMF.<p> / Doctorat en Sciences de la santé publique / info:eu-repo/semantics/nonPublished

Ectopic calcification can cause pain and limit mobility. Studies suggest that circadian genes may play a role in the calcification process. Core circadian genes Clock, Npas2, and Bmal1 are transcription factors that form CLOCK:BMAL1 or NPAS2:BMAL1 transactivator complexes that drive the rhythmic expression of circadian oscillator genes and output genes. Circadian oscillator genes Period1-3 and Cryptochrome1-2 encode proteins that form transcription repressor complexes that feedback to inhibit CLOCK/NPAS2:BMAL1 activity, thus completing the feedback loop that is the basis of the molecular circadian clockwork. Arrhythmic Bmal1-/- mice exhibit site-specific, age-dependent arthropathy. While studying the circadian phenotype of Clock-/-;Npas2m/m double mutant mice, we discovered that these double mutant mice develop site-specific arthropathy similar to the arthropathy described in Bmal1-/- mice. Based on the circadian clockwork mechanism, we hypothesized that CLOCK/NPAS2:BMAL1 transactivator complexes drive the expression of a gene (or genes) that prevents age-dependent arthropathy. To investigate Clock-/-;Npas2m/m double mutant mouse arthropathy, we evaluated mutant mice using X-ray, micro-computed tomography, and histology, and found that Clock-/-;Npas2m/m double mutant mice exhibit age-dependent, site-specific arthropathy that phenocopies that of Bmal1-/- mice. The costosternal junction and calcaneal tendon are most prominently affected, in that calcification of those tissues is detectable as early as 4-5 weeks and 11-12 weeks, respectively. The arthropathic lesions in these tissues consist of calcium phosphate vii deposits, and in Bmal1-/- costosternal junction calcifications, the deposits contain calcium pyrophosphate dihydrate crystals. Mechanical stress, disregulation of centrally-regulated circadian rhythms, and systemic serum mineral imbalances likely do not contribute to this pathology. In vitro micromass cultures generated from Clock-/-;Npas2m/m double mutant mouse embryonic fibroblasts do not exhibit irregular chondrocyte differentiation compared to wild-type cultures, suggesting that chondrocyte cell-autonomous mechanisms are insufficient to induce this arthropathy. Analysis of Clock-/-;Npas2m/m double mutant intersternebral tissue RNA did not reveal significant changes in chondrocyte or calcification-related gene expression. Histological stains showed an absence of osteoblasts and osteoclasts around costosternal junction calcifications, suggesting that these cell types are not contributing to this pathology. Instead, chondrocytes are localized to the costosternal junction but there were no significant changes in the distribution of chondrocyte markers in this tissue, as evaluated by immunohistochemistry. These findings suggest that Clock or Npas2, and Bmal1, regulate ectopic calcification through a combination of systemic and local factors, and that the cells affected by Clock and Npas2, or Bmal1, disruption are a subset of the cells distributed in specific tissues that develop age-dependent arthropathy. The significance of these findings is that “circadian genes” play a role in the regulation of ectopic calcification in a non-oscillator capacity. Understanding this new mechanism by which ectopic calcification is controlled could lead to novel approaches for the treatment of some human calcification diseases.