bioRxiv Science⌕ Search

Biology subjects

Maden, M.

Publications and source records attributed to Maden, M..

5 recordsLinked to original sources

Insights into the evolution of dermal armour: osteoderms in a mammal, the spiny mouse, Acomys.

Osteoderms are bony plates which develop in the dermis of the skin of vertebrates, most commonly found in fishes and reptiles. They have evolved independently at least eight times in reptiles suggesting the presence of a gene regulatory network which is readily activated and inactivated. The absence of osteoderms in birds and mammals, except for the one example of armadillos, has prevented a comparative molecular approach to their evolution. However, following CT scanning, we have discovered that in two genera of Deomyinae, the spiny mouse Acomys and the brush-furred mouse, Lophuromys there are osteoderms present in the skin of their tails. We have studied osteoderm development within the dermis of the tail in Acomys cahirinus to show that they begin development before birth in the proximal part of the tail skin and they do not complete differentiation throughout the tail until 6 weeks after birth. This has allowed us to study the cellular differentiation of the osteoderms with histology and immunocytochemistry and perform RNA sequencing to identify the gene networks involved in their differentiation. There is a widespread down-regulation of keratin genes and an up-regulation of osteoblast genes and a finely balanced expression of signaling pathways as the osteoderms differentiate. Future comparisons with reptilian osteoderms may allow us to understand how these structures have evolved, why they are so rare in mammals and how they are position-specific.

evolutionary biology↗

Social dominance status and social stability in spiny mice (Acomys cahirinus) and its relation to ear-hole regeneration and glucocorticoids

Spiny mice (Acomys cahirinus) are an emerging animal model in studies measuring tissue regeneration, but decades of research on social dominance in other animals indicates the relationships animals form in their home-cage may affect phenotypic plasticity in tissue regeneration and glucocorticoids. Studies in baboons and mice, for example, indicate that subordinate ranked animals heal wounds slower than their dominant group-mates, and have increased levels of basal glucocorticoids. Recent studies in tissue regeneration with salamanders and zebrafish indicate that increased glucocorticoids can delay tissue regeneration, but whether this effect extends to Acomys is unknown, especially regarding their social dominance relationships. Here we report that most adult Acomys had a social dominance status, but many groups had unclear social stability, with more frequent huddling than fighting during their active cycle. We also found no sex differences in social dominance behavior, and that Acomys more frequently fled than froze when chased or approached. After a 4mm ear-pinna biopsy, we found that social stability significantly accounted for variability in time to close the ear-hole but adding age to the statistical model removed the effect of social stability. When investigating glucocorticoid blood levels, there were no significant effects of social dominance status or social stability. A transcriptional enhancer for StAR, Nr5a1 had a significant effect for the interaction of social dominance status and social stability. This effect, however, was not reflected in StAR and unclear groups mostly had unclear social statuses, so this effect should be considered with caution. This is the first study to investigate home-cage social dominance behaviors in Acomys since the 1970s or measure any associations with their ability to regenerate tissue. This provides a platform for further work on their social dominance and glucocorticoids and highlights the need to consider the role of aging in their ability to regenerate tissue.

animal behavior and cognition↗

Design, construction, and advantages of 100% online laboratories in an upper division undergraduate biology course

For centuries, students have been taught by passively listening to lectures, usually in large groups. In many fields, this type of course delivery is not ideal. In addition, students that have grown up with online access and/or have been forced to take online course during the recent pandemic, are seeking improved online educational experiences. As providers of education, Universities must adapt to this rapidly changing environment. The emergence of exciting, "disruptive" technologies has provided the tools needed for educators to revolutionize the delivery of higher education. The University of Florida, through UF Online, provides students the opportunity to enroll in fully online four-year undergraduate degrees. In this report, we describe the development of fully online laboratories for the upper-division course Evolutionary Developmental Biology, which fulfill the University of Floridas laboratory requirement. This course is taken by Biology, Zoology, and related majors, including majors in the 100% online Biology degree. The experiments in the virtual laboratories would have been impossible to teach in a residential setting due to time constraints, cost, student safety issues, and regulatory/certification requirements. The ability to perform these experiments online provided University of Florida undergraduates located throughout the world access to unique, one-of-a-kind laboratory experiences. The virtual laboratories allowed students to undertake in-depth exploration and application of course content that is not possible in a residential setting. Completion of the Evolutionary Developmental Biology course provided undergraduate students the opportunity to obtain a science degree without ever visiting the universitys residential campus. During the Fall 2020 term, this course was made available to residential students, thus allowing this cohort of students to continue to make progress, 100% online, towards their undergraduate degree during the COVID19 pandemic.

developmental biology↗

Spiny mice (Acomys) exhibit attenuated hallmarks of aging and rapid cell turnover after UV exposure in the skin epidermis

The study of long-lived and regenerative animal models has revealed diverse protective responses to stressors such as aging and tissue injury. Spiny mice (Acomys) are a unique mammalian model of skin regeneration, but their response to other types of physiological skin damage have not been investigated. In this study, we examine how spiny mice skin responds to acute UVB damage or chronological aging compared to non-regenerative C57Bl/6 mice (M. musculus). We find that, compared to M. musculus, the skin epidermis in A. cahirinus experiences a similar UVB-induced increase in basal cell proliferation but exhibits increased epidermal turnover. Notably, A. cahirinus uniquely form a suprabasal layer co-expressing Keratin 14 and Keratin 10 after UVB exposure concomitant with reduced epidermal inflammatory signaling and reduced markers of DNA damage. In the context of aging, old M. musculus animals exhibit typical hallmarks including epidermal thinning, increased inflammatory signaling and senescence. However, these age-related changes are absent in old A. cahirinus skin. Overall, we find that A. cahirinus have evolved novel responses to skin damage that reveals new aspects of its regenerative phenotype.

cell biology↗

Molecular and histologic outcomes following spinal cord injury in spiny mice, Acomys cahirinus

The spiny mouse (Acomys cahirinus) appears to be unique among mammals by showing little scarring or fibrosis after skin or muscle injury, but the Acomys response to spinal cord injury (SCI) is unknown. We tested the hypothesis that Acomys would have molecular and immunohistochemical evidence of reduced spinal inflammation and fibrosis following SCI as compared to C57BL/6 mice (Mus), which similar to all mammals studied to date exhibits spinal scarring following SCI. Initial experiments used two pathway-focused RT-PCR gene arrays (\"wound healing\" and \"neurogenesis\") to evaluate tissue samples from the C2-C6 spinal cord 3-days after a C3/C4 hemi-crush injury (C3Hc). Based on the gene array, specific genes were selected for RT-qPCR evaluation using species-specific primers. The results supported our hypothesis by showing increased inflammation and fibrosis related gene expression (Serpine 1, Plau, Timp1) in Mus as compared to Acomys (P<0.05). RT-qPCR also showed enhanced stem cell and axonal guidance related gene expression (Bmp2, GDNF, Shh) in Acomys compared to Mus (P<0.05). Immunohistochemical evaluation of the spinal lesion at 4-wks post-injury indicated reduced collagen IV immunostaining in Acomys (P<0.05). Glial fibrillary acidic protein (GFAP) and ionized calcium binding adaptor molecule 1(IBA1) immunostaining indicated morphological differences in the appearance of astrocytes and macrophages/microglia in Acomys. Collectively, the molecular and histologic results support the hypothesis that Acomys has reduced spinal inflammation and fibrosis following SCI. We suggest that Acomys may be a useful comparative model to study adaptive responses to SCI.\n\nHighlightsO_LISpiny mice (Acomys cahirinus) and C57BL/6 (Mus) were studied after spinal injury\nC_LIO_LIRT-PCR gene arrays suggested different molecular response in Acomys\nC_LIO_LIRTq-PCR with species-specific primers showed increased neurogenesis-related signaling\nC_LIO_LIHistology indicates reduced scarring and fibrosis in Acomys\nC_LIO_LIAcomys may be a useful comparative model to study SCI\nC_LI

neuroscience↗