Assessing the unidimensionality of Clayton’s Environmental Identity Scale using Confirmatory Factor Analysis (CFA) and Bifactor Exploratory Structural Equation Modeling (bifactor-ESEM)

Researche article available on the publisher's website Collections: Section: Social PsychologyCorrespondence concerning this article should be addressed to Prof. Paulo Moreira, Instituto de Psicologia e de Ciências da Educação, Universidade Lusíada, Rua de Moçambique 21 e 71, Porto 4100-348, Portugal. Email: [email protected] relevant intrapersonal characteristic for understanding intentions and behavior toward environmental sustainability is the degree to which nature is important for a person’s self-definition. Clayton’s Environmental Identity (EID) scale purports to measure this construct. However, a limited number of prior exploratory studies of this measure have supported different factor structures. Hence, our initial aim was to develop an understanding of the dimensionality of Clayton’s 24-item EID scale by testing competing latent structures using confirmatory factor analysis. We analyzed self-reported data from 458 adults (Mage = 26.7 years; 81% female). Four a priori models (a first-order model, a second-order model, a unidimensional model, and a bifactor model) did not show satisfactory fit to the data. An ancillary analysis using bifactor exploratory structural equation modeling (bifactor-ESEM) indicated a bifactor model with three specific factors had a good fit to the data. The factor loadings of this model and values for bifactor indices (Omega Hierarchical and Explained Common Variance [ECV]) indicated a single mean score across all EID scale items taps into an essentially unidimensional construct and is therefore appropriate to interpret. In sum, our study provides a critical insight into the dimensionality of Clayton’s EID scale that will be valuable when applying this measure for research and intervention purposes

Anthropometric Characteristics, Body Composition and Somatotype of Elite Pan-American Race Walking 20K

The anthropometric and somatotype evaluation is an essential tool in the selection and control of high-performance athletes. The aim of this study was to describe the somatotype and body composition of male elite race walkers (20 k modality), and its relationship with athletic performance. Twenty-four race walkers participated in this study. The sample was divided into two groups: the race walkers with the best performance (upper 25 percentile; n=7) and the second group (n=17) that corresponds to the rest of the participants. Weight (kg), height (cm), seven skinfolds, two diameters and five perimeters were measured. Body fat percentage (BF%) were estimated with the Yuhasz formula, and the somatotype was used applying the Heath-Carter method. The best performing athletes were taller (178.3 +/- 4.4 cm vs. 173.7 +/- 5.6 cm, p<0.05) and showed a greater ectomorphic component (p<0.05) than the rest of the participants. The somatotype of the best performance athletes was 2.2-2.8-4.1 against the 2.5-3.8-2.9 of the lowest performing athletes. The average time (hours, minute, seconds) of execution of the race in athletes of better performances was 1: 22:40, in comparison with the athletes of lower performances with 1: 32: 41 (p<0.02). The ectomorphic component and height are morphological characteristics that can determine athletic performance of race walkers. It is suggested to consider these factors in the selection of the race walkers. La evaluación antropométrica y del somatotipo es una importante herramienta en la selección y control de los atletas de alto rendimiento. El objetivo de este estudio fue describir el somatotipo y composición corporal de hombres marchistas olímpicos, modalidad 20 k, y su relación con el rendimiento atlético. Veinticuatro atletas de marcha participaron en este estudio. La muestra fue dividida en dos grupos: los marchistas de mejores rendimientos p25 superior (n=7) y el segundo grupo (n=17) que corresponde al resto de los participantes. Se registró el peso (kg), talla (cm), siete pliegues cutáneos, dos diámetros y cinco perímetros. Se estimó el porcentaje de grasa corporal (%GC) con la fórmula de Yuhasz y se describió el somatotipo utilizando el método de Heath-Carter. Se reporta una mayor altura en los atletas de mejor rendimiento (178,3±4,4 cm vs. 173,7±5,6 cm; p<0,05) y mayor componente ectomorfico (p<0,05) que el resto de los participantes. El somatotipo de los atletas de mejor rendimiento fue de 2.2-2.8-4.1 frente al 2.5-3.8-2.9 de los atletas de menor rendimiento. El tiempo promedio (hora, minuto, segundo) de ejecución de la carrera en atletas de mejores rendimientos fue de 1:22:40, en comparación con los atletas de menores rendimientos con 1:32:41 (p <0,02). El componente ectomórfico y altura serian características morfológicas que pueden determinar el rendimiento deportivo de atletas de marcha. Se sugiere considerar estos factores en la selección de los marchistas olímpicos

Matrix Assisted Laser Desorption Ionization (MALDI) Mass Spectrometry: An Imaging Modality to Monitor the Effects of Gene Therapy in a Murine Model of GM1 Gangliosidosis

GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder caused by an enzyme deficiency of β-galactosidase (β-gal) leading to toxic accumulation of GM1 ganglioside in the central nervous system (CNS) and progressive neurodegeneration. Adeno-associated virus (AAV) mediated gene delivery of lysosomal enzymes to the CNS has shown great potential for the treatment of lysosomal storage diseases with neurological involvement. In this work we use MALDI mass spectrometry imaging (MSI) to assess the spatial distribution of gangliosides, ganglioside metabolites and related lipids in a GM1 gangliosidosis mouse brain model following adeno-associated virus (AAV) gene therapy. Deficiency of β-galactosidase enzyme in a β-gal-/- mouse brain showed an overall 8-fold increase in GM1 relative to the control by MSI analysis, with specific spatial localization based on its ceramide content. Bilateral thalamic injection of AAVrh10-bgal in β-gal-/- mice significantly reduced GM1 levels relative to untreated β-gal-/- mice. The therapeutic efficacy of this approach is through distribution of functional enzyme via axonal transport through the extensive connectivity of the thalamus with most of the brain, with some exceptions such as the temporal cortex. Accordingly MSI showed AAV gene therapy reduced GM1 nearly to the control levels in all regions of the brain except in the temporal cerebral cortex. This correlated with low levels of bgal in this brain region as assessed by histochemical staining of tissue sections. MSI also detected asialo-GM1 and other ganglioside metabolites elevated in untreated β-gal-/- mice, which were also reduced after AAV therapy. Interestingly sulfated galactocereberosides reduced in the myelin sheath in untreated β-gal-/- mice were restored to normal levels after AAV therapy. Overall, this study demonstrates that MALDI MSI can be used to map specific target analytes and their metabolites while also offering the ability to detect unanticipated effects caused by gene therapy

Megakaryocytes: Regulators of Bone Mass and Hematopoiesis

poster abstractEmerging evidence demonstrates that megakaryocytes (MK) play a key role in regulating skeletal homeostasis and hematopoiesis. Recent reports show that MK reside in close proximity to hematopoietic stem cells (HSC). Genetic depletion of MK resulted in mitotic activation of HSC suggesting that MK maintain HSC quiescence. Other studies demonstrated that following irradiation, surviving MK migrate to endosteal surfaces where osteoblast (OB) lineage cells dramatically increase and promote engraftment of transplanted HSC. Here we investigated if MK directly impact hematopoiesis or whether they indirectly support HSC function through their interaction with OB-lineage cells. Our data suggests that LSK (Lin-Sca+CD117+, an enriched HSC population) co-cultured with MK and OB generate significantly higher numbers of colony forming cells (HSC function) compared to LSK cocultured with either MK or OB alone. The functionality of this in vitro data was confirmed in vivo with transplantation studies which showed increased engraftment in mice transplanted with LSK cells co-cultured with OB and MK compared to LSK cells co-cultured with OB alone. To test if loss of MK negatively impacts osteoblastogenesis, we generated conditional knockout mice where cMpl, the receptor for the main MK growth factor, thrombopoietin (TPO), was deleted in MK (cMplfl/fl x PF4Cre). Unexpectedly, these mice exhibited a 10-fold increase in platelet numbers, megakaryocytosis, a dramatic expansion of phenotypically defined hematopoietic precursors, and a remarkable 20-fold increase in the bone volume fraction. Collectively, these data indicate that while MK modulate HSC function, this activity is in part mediated through interactions with OB and suggest a complex role for TPO and MK in HSC regulation. While work is needed to further elucidate mechanisms, understanding the coordinated interaction between MK, OB, HSC, and TPO/Mpl should inform the development of novel treatments to enhance HSC recovery following myelosuppressive injuries, as well as bone loss diseases, such as osteoporosis

Scaffold-free bioprinting of mesenchymal stem cells using the Regenova printer: Spheroid characterization and osteogenic differentiation

Limitations in scaffold material properties, such as sub-optimal degradation time, highlight the need for alternative approaches to engineer de novo tissues. One emerging solution for fabricating tissue constructs is scaffold-free tissue engineering. To facilitate this approach, three-dimensional (3D) bioprinting technology (Regenova Bio 3D Printer) has been developed to construct complex geometric shapes from discrete cellular spheroids without exogenous scaffolds. Optimizing spheroid fabrication and characterizing cellular behavior in the spheroid environment are important first steps prior to printing larger constructs. Here, we characterized spheroids of immortalized mouse bone marrow stromal cells (BMSCs) that were differentiated to the osteogenic lineage. Immortalized BMSCs were seeded in low attachment 96-well plates in various numbers to generate self-aggregated spheroids either under the force of gravity or centrifugation. Cells were cultured in control or osteogenic media for up to 28 days. Spheroid diameter, roundness and smoothness were measured. Cell viability, DNA content and alkaline phosphatase activity were assessed at multiple time points. Additionally, expression of osteogenic markers was determined using real time qPCR. Spheroids formed under gravity with 20 K, 30 K and 40 K cells had average diameters of 498.5 ± 8.3 μm, 580.0 ± 32.9 μm and 639.2 ± 54.0 μm, respectively, while those formed under 300G centrifugation with the same numbers of cells had average diameters of 362.3 ± 3.5 μm, 433.1 ± 6.4 μm and 491.2 ± 8.0 μm. Spheroids formed via centrifugation were superior to those formed by gravity, as evidenced by better roundness and smoothness and double the retention of DNA (cellular) content. Cells in spheroids exhibited a robust osteogenic response to the differentiation medium, including higher mRNA expression of alkaline phosphatase, collagen type I, and osteocalcin than those cultured in control medium, as well as greater alkaline phosphatase activity. The optimal spheroid fabrication technique from this study was to aggregate 40 K cells under 150–300G centrifugation. In future investigations, these spheroids will be 3D printed into larger tissue constructs

Microwave Assisted Synthesis of Py-Im Polyamides

Microwave synthesis was utilized to rapidly build Py-Im polyamides in high yields and purity using Boc-protection chemistry on Kaiser oxime resin. A representative polyamide targeting the 5′-WGWWCW-3′ (W = A or T) subset of the consensus Androgen and Glucocorticoid Response Elements was synthesized in 56% yield after 20 linear steps and HPLC purification. It was confirmed by Mosher amide derivatization of the polyamide that a chiral α-amino acid does not racemize after several additional coupling steps

The proto‐oncogene function of Mdm2 in bone

Mouse double minute 2 (Mdm2) is a multifaceted oncoprotein that is highly regulated with distinct domains capable of cellular transformation. Loss of Mdm2 is embryonically lethal, making it difficult to study in a mouse model without additional genetic alterations. Global overexpression through increased Mdm2 gene copy number (Mdm2Tg) results in the development of hematopoietic neoplasms and sarcomas in adult animals. In these mice, we found an increase in osteoblastogenesis, differentiation, and a high bone mass phenotype. Since it was difficult to discern the cell lineage that generated this phenotype, we generated osteoblast‐specific Mdm2 overexpressing (Mdm2TgOb) mice in 2 different strains, C57BL/6 and DBA. These mice did not develop malignancies; however, these animals and the MG63 human osteosarcoma cell line with high levels of Mdm2 showed an increase in bone mineralization. Importantly, overexpression of Mdm2 corrected age‐related bone loss in mice, providing a role for the proto‐oncogenic activity of Mdm2 in bone health of adult animals