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Jo-Ann L Stanton

Publications and source records attributed to Jo-Ann L Stanton.

4 recordsLinked to original sources

Nerve growth factor mRNA expression in the regenerating antler tip of red deer (Cervus elaphus).

Deer antlers are the only mammalian organs that can fully regenerate each year. During their growth phase, antlers of red deer extend at a rate of approximately 10 mm/day, a growth rate matched by the antler nerves. It was demonstrated in a previous study that extracts from deer velvet antler can promote neurite outgrowth from neural explants, suggesting a possible role for Nerve Growth Factor (NGF) in antler innervation. Here we showed using the techniques of Northern blot analysis, denervation, immunohistochemistry and in situ hybridization that NGF mRNA was expressed in the regenerating antler, principally in the smooth muscle of the arteries and arterioles of the growing antler tip. Regenerating axons followed the route of the major blood vessels, located at the interface between the dermis and the reserve mesenchyme of the antler. Denervation experiments suggested a causal relationship exists between NGF mRNA expression in arterial smooth muscle and sensory axons in the antler tip. We hypothesize that NGF expressed in the smooth muscle of the arteries and arterioles promotes and maintains antler angiogenesis and this role positions NGF ahead of axons during antler growth. As a result, NGF can serve a second role, attracting sensory axons into the antler, and thus it can provide a guidance cue to define the nerve track. This would explain the phenomenon whereby re-innervation of the regenerating antler follows vascular ingrowth. The annual growth of deer antler presents a unique opportunity to better understand the factors involved in rapid nerve regeneration.

Amino Acid Sequence↗

The organic osmolytes betaine and proline are transported by a shared system in early preimplantation mouse embryos.

Betaine and proline protect preimplantation mouse embryos against increased osmolarity and decreased cell volume, implying that they may function as organic osmolytes. However, the transport system(s) that mediates their accumulation in fertilized eggs and early embryos was unknown, and previously identified mammalian organic osmolyte transporters could not account for their transport. Here, we report that there is a single saturable transport component shared by betaine and proline in 1-cell mouse embryos. A series of inhibitors had nearly identical effects on both betaine and proline transport by this system. In addition, K(i) values for reciprocal inhibition of betaine and proline transport were approximately 100-300 microM, similar to K(m) values ( approximately 200-300 microM) for their transport, and both had similar maximal transport rates (V(max)). The K(i) values for inhibition of betaine and proline transport by dimethylglycine were similar ( approximately 2 mM), further supporting transport of both substrates by a single transport system. Finally, betaine and proline transport each required Na(+)- and Cl(-). These data were consistent with a single, Na(+)- and Cl(-)-requiring, betaine/proline transport system in 1-cell mouse embryos. While betaine was only transported by a single saturable system, we found an additional, less conspicuous proline transport route that was betaine-insensitive, Na(+)-sensitive, and inhibited by alanine, leucine, cysteine, and methionine. Furthermore, we showed that betaine, like proline, is present in the mouse oviduct and thus could serve as a physiological substrate. Finally, accumulation of both betaine and proline increased with increasing osmolarity, consistent with a possible role as organic osmolytes in early embryos.

Alanine↗

Gene expression in the mouse preimplantation embryo.

Mouse preimplantation development represents a tightly controlled programme of gene expression and cell division, which starts with the fertilized egg and ends with implantation of the blastocyst approximately 4.5 days later. Spatial and temporal differences in gene expression underpin establishment of axes at the two-cell stage and development of the trophectoderm and inner cell mass after embryo compaction at the eight-cell stage. Approximately 15 700 mouse genes expressed during preimplantation development have been identified from cDNA sequences deposited in the UniGene database of the National Institutes of Health. This inventory of preimplantation genes is the starting point for identifying signalling modules that function in preimplantation development.

Animals↗

Identifying tissue-enriched gene expression in mouse tissues using the NIH UniGene database.

There is considerable interest in the gene expression profiles that underpin the phenotypes of cells and tissues. We have developed Bioperl scripts for mining the National Institutes of Health (NIH) UniGene databases to identify this tissue-enriched gene expression. UniGene imports expressed sequence tags (ESTs) from the NIH dbEST database and clusters them by searching for sequence matches. In principle, each UniGene cluster represents the product(s) of a single transcriptional unit in the genome. This transcriptional unit can be expressed in a range of cell types, and UniGene clusters reflect these heterogeneous origins. UniGene clusters containing ESTs expressed predominantly or uniquely by one tissue will show a high proportion of ESTs from that tissue. Our Bioperl scripts parse the NIH UniGene data files as a starting point for an in-house UniGene database. Each UniGene cluster is then assessed for the total number of ESTs from a specified set of dbEST libraries and the total number of ESTs in the cluster. The ratio of the two gives a measure of enrichment. In this paper, we identify tissue-enriched gene expression in mouse pancreas, mammary gland and heart. Each tissue-enriched expression profile identifies genes that are recognisably characteristic of the respective tissue. It also identifies significant numbers of tissue-enhanced UniGenes that are derived from transcriptional units with no known function. These genes may play important and specialised functions in the tissue in question and offer targets for drug action.

Animals↗