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In male rats gubernacular cones develop during the latter half of prenatal life. Inversion of these papilla-like organs after birth is the first step to postnatal growth of the muscular cremaster sacs. The factors regulating prenatal growth and differentiation or postnatal inversion of these gubernacular cones are unknown. The lack of a detailed and unequivocal description of the normal gubernacular cone growth is judged at least partially responsible for this ignorance. The present study therefore describes the normal development of the gubernacular cones in male and female rats from day 14 of fetal life. Androgens are hypothesized to control male gubernacular cone development but recent evidence throws doubt upon this proposal. Therefore, the second part of this study describes perinatal development of gubernacular cones in male rat foetuses exposed to the anti-androgen flutamide from day 10 after conception. Quantitatively normal growth occurred prior to birth, indicating no role of androgen in this process. Excessive growth in length was noticed during the neonatal period together with delay of gubernacular cone inversion. These developmental alterations did not represent direct anti-androgen-induced modifications of gubernacular cones development as the alterations were not observed in flutamide-exposed neonatally castrated animals. Failure of androgens to affect directly perinatal gubernacular cone growth could represent a rat-specific feature. Fetal rabbits show the development of similar structures during the second half of fetal life.(ABSTRACT TRUNCATED AT 250 WORDS)
Anat Rec 1993 Jun
PMID:Perinatal development of gubernacular cones in rats and rabbits: effect of exposure to anti-androgens. 833 43

The effects of pretreatment with androgen or thyroid hormone on androgen-induced proliferation of granular convoluted tubular cells (GCT cells) in the submandibular glands of ovariectomized female BALB/c or C57BL/6 mice were investigated. The proliferation of GCT cells was estimated by their labeling index. Daily injections of 5 alpha-dihydrotestosterone (DHT) (100 micrograms/mouse/day) caused a transient increase in the labeling index of GCT cells of ovariectomized 60-day-old BALB/c mice during the first four injections, but injections of thyroxine (T4) (15 micrograms/mouse/day) did not. On the other hand, both DHT and T4 increased the esteroprotease activity, a marker of the differentiation of GCT cells, time dependently. Injections of DHT into ovariectomized 102-day-old BALB/c mice also caused a transient increase in the labeling index of GCT cells. However, pretreatment of ovariectomized 60-day-old BALB/c mice with DHT for 4 or 14 days completely abolished the DHT-induced increase in the labeling index of 102-day-old mice, and pretreatment with T4 for 14 days reduced this increase. Pretreatment with DHT or T4 for 14 days did not affect the DHT-induced increase in esteroprotease activity. Pretreatment of ovariectomized 60-day-old C57BL/6 mice with DHT for 14 days also completely abolished the DHT-induced increase in the labeling index of GCT cells at the age of 102 days, but pretreatment with T4 for 14 days did not affect the increase.(ABSTRACT TRUNCATED AT 250 WORDS)
Anat Rec 1993 Aug
PMID:Effects of pretreatment with androgen or thyroid hormone on androgen-induced proliferation of granular convoluted tubular cells in mouse submandibular glands. 837 91

Vascular smooth muscle cells (SMCs) originate from multiple types of progenitor cells. In the embryo, the most well studied SMC progenitor is the cardiac neural crest stem cell. Smooth muscle differentiation in the neural crest lineage is controlled by a combination of cell intrinsic factors, including Pax3, Tbx1, FoxC1, and serum response factor, interacting with various extrinsic factors in the local environment such as bone morphogenetic proteins (BMPs), Wnts, endothelin (ET)-1, and FGF8. Additional sources of multipotential cells that give rise to vascular SMCs in the embryo include proepicardial cells and possibly endothelial progenitor cells. In the adult, vascular SMCs must continually repair arterial injuries and maintain functional mass in response to changing demands upon the vessel wall. Recent evidence suggests that this is accomplished, in part, by recruiting multipotential vascular progenitors from bone marrow-derived stem cells as well as from less well defined sources within adult tissues themselves. This article will review our current understanding of the origins of vascular SMCs from multipotential stem and progenitor cells in developing as well as adult vasculature.
Anat Rec A Discov Mol Cell Evol Biol 2004 Jan
PMID:Smooth muscle stem cells. 1469 31