From the early steps of whisker formation to its evolutionary disappearance: the (curious) case of Prdm1 and its regulation
Whiskers (also known as vibrissae) are sensory organs that are thought to have first appeared in Therapsida, a group of synapsids that includes mammals and evolutionary ancestors like the Thrinaxodon(1). They are highly conserved among mammals to the notable exception of the higher primates and are...
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Zusammenfassung: | Whiskers (also known as vibrissae) are sensory organs that are thought to have first appeared in Therapsida, a group of synapsids that includes mammals and evolutionary ancestors like the Thrinaxodon(1). They are highly conserved among mammals to the notable exception of the higher primates and are important for behavior, especially for nocturnal animals and the ones living in burrows(2). Furthermore, the mechanoreceptors of the vibrissae signal to the primary somatosensory cortex, where a discrete and well-defined structure in layer 4 represents each whisker(3). This structure, known as barrel cortex, occupies a large portion of the rodent brain. Strikingly, Prdm1 conditional KO (cKO) mice are one of the rare transgenic strains that do not develop whiskers while forming a pelage; on the other hand, the other head structures expressing Prdm1 (including pelage hair follicles and teeth) grow normally(4). In the developing whisker pad, Prdm1 expression is confined to the mesenchyme underlying the embryonic epidermis that will later form the whisker epidermal placode; it lasts until dermal papilla formation, when a âswitchâ occurs to the precursors of the inner root sheath. The Prdm1 ablation study we conducted revealed the absence of the patterned up-regulation of Bmp2 (marker of placode formation), Shh (a protein secreted by the epidermal placode responsible for the first epidermal signal) and Bmp4 (expressed in the pre-follicle mesenchyme). On the other hand, Lef1 is expressed uniformly in the mesenchyme of the whisker pad, thus pointing out the integrity of the βCatenin-mediated first mesenchymal signal. Those results suggest the role of Prdm1 as a master gene in whisker development. Prdm1 expressing cells are mainly non-proliferative; however, a small subpopulation at the periphery is cycling. Being Sox2 coexpressed with Prdm1 in the whisker mesenchyme, we performed lineage tracing with Sox2CreERT2 and ROSAYFP transgenic strains. Those experiments revealed that Sox2/Prdm1 expressing cells contribute to the formation of the dermal papilla, dermal sheath and putative pericytes of the whisker follicle and thus constitute a population of embryonic progenitors crucial for whisker formation. We subsequently investigated the development of the barrel cortex in our cKO mice. Intriguingly, a disorganized pattern was observed in cKO mice, suggesting that the loss of expression of a single gene, and consequently the disappearance of vibrissae, drastically impac |
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DOI: | 10.5075/epfl-thesis-6984 |