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Biology subjects

Binder, M. D.

Publications and source records attributed to Binder, M. D..

2 recordsLinked to original sources

Roles of TYRO3 Family Receptors in Germ Cell Development During Mouse Testis Formation

Structured AbstractO_ST_ABSObjectiveC_ST_ABSTo investigate the role of a potential SOX9 target gene, Tyro3, along with its family members, Axl and Mertk (TAM family) in mouse testis development. DesignExperimental laboratory study. SettingResearch institute units. Subject(s)Embryonic day (E)11.5 Swiss mouse gonads for ex vivo gonad culture; Tyro3 knockout mouse embryos. Intervention(s)E11.5 Swiss mouse gonads were cultured in hanging droplets of 30 {micro}L DMEM medium supplemented with 10% FBS and 1% antibiotic-antimycotic. A pair of gonads were treated with 20 M of BMS-777607 or 30 M of LDC1267 and an equivalent volume of the vehicle control DMSO. Main Outcome Measure(s)Immunofluorescence to measure morphological changes of ex vivo cultured gonads and in vivo Tyro3 mouse testes; qRT-PCR to measure gene expressions. Result(s)Inhibition of the TAM family in E11.5 ex vivo cultured male mouse gonads led to reduced germ cell numbers caused by reduced proliferation and increased apoptosis of the germ cells. Tyro3 knockout mice exhibited reduced expression levels of the germ cell genes Ddx4, Dazl and Pou5f1 and increased expression levels of the Sertoli cell genes Sox9 and Amh at E12.5. However, by E14.5, the expression of Ddx4, Dazl, Sox9 and Amh had returned to normal levels in Tyro3 knockout testes. Tyro3 knockout testes displayed normal morphology and structures during fetal testis development. Conclusion(s)TAM family members have redundant roles in regulating germ cell development during early testis development. Attestation StatementO_LIData regarding any of the subjects in the study has not been previously published unless specified. C_LIO_LIData will be made available to the editors of the journal for review or query upon request. C_LI Data Sharing StatementN/A CapsuleInhibition of the TAM family led to loss of germ cells in fetal gonads and deletion of Tyro3 alone disturbed gene expressions of germ cells and Sertoli cells.

developmental biology↗

Mouse microglia express unique miRNA-mRNA networks to facilitate age-specific functions in the developing central nervous system

Microglia regulate multiple processes in the central nervous system, exhibiting a significant level of cellular plasticity which is facilitated by an equally dynamic transcriptional environment. While many gene networks that regulate microglial functions have been characterised, the influence of epigenetic regulators such as small non-coding microRNAs (miRNAs) is less well defined. We have sequenced the miRNAome and mRNAome of mouse microglia during brain development and adult homeostasis, identifying unique profiles of known and novel miRNAs. Microglia express both a consistently enriched miRNA signature as well as temporally distinctive subsets of miRNAs. We generated robust miRNA-mRNA networks related to fundamental developmental processes, in addition to networks associated with immune function and dysregulated disease states. There was no apparent influence of sex on miRNA expression. This study reveals a unique developmental trajectory of miRNA expression in microglia during critical stages of CNS development, establishing miRNAs as important modulators of microglial phenotype.

neuroscience↗