Abstract

The mechanisms underlying the initiation of puberty, one of the cornerstones of human evolution, have not been fully elucidated as yet. However, recently, an accumulating body of evidence has helped unravel several critical aspects of the process. It is clear that a change in the pattern of pituitary gonadotropin secretion serves as a hormonal trigger for puberty induction. This change is directly guided by the hypothalamic GnRH pulse generation, a phenomenon regulated by the Kisspeptin-Neurokinin-Dynorphin (KNDy) system also in the hypothalamus. This represents the kisspeptin molecule, which is crucial in augmenting GnRH secretion at puberty, whose secretion is fine-tuned by the opposing signals neurokinin B and dynorphin. Recently, the novel kisspeptin inhibitory signal MKRN3 was described, whose role in puberty initiation provided further insight into the mechanistic aspects of pubertal onset. Furthermore, the description of higher inhibitory and stimulatory signals acting upstream of the KNDy neurons suggested that the trigger point of puberty is located upstream of the KNDy system and the GnRH pulse generator. However, the mechanism of pubertal onset should not be considered as an isolated closed loop system. On the contrary, it is influenced by such factors as adipose tissue, gastrointestinal function, adrenal androgen production, energy sensing, and physical and psychosocial stress. Also, fetal and early life stressful events, as well as exposure to endocrine disruptors, may play important roles in pubertal initiation, the latter primarily through epigenetic modifications. Here we present the available data in the field and attempt to provide an integrated view of this unique and crucial phenomenon.

Highlights

  • According to Webster’s dictionary, puberty is defined as “the period of first becoming capable of reproducing, and is marked by maturation of the genital organs, development of secondary sex characteristics, acceleration in linear growth velocity, changes in affect, and, in the female, the occurrence of menarche.” It is obvious that this period of quick and radical changes of human physiology, as well as of psychosocial and psycho-behavioral functions, is regulated by hormonal mechanisms

  • Its central role in the natural course of puberty is emphasized by the observation made through a large genome-wide analysis study (GWAS), that single-nucleotide polymorphisms (SNPs) of the MKRN3 region affect the age of menarche in healthy girls [18]

  • The action of leptin on pubertal onset is essential but permissive rather than regulatory, granted that in patients with lipodystrophies, where minimal amounts of leptin are produced, pubertal development is normal [50]. Another factor related to adipose tissue is DLK1, or preadipocyte factor 1 (Pref-1), which is a transmembrane protein encoded by an imprinted, paternally expressed gene: it is located on the long arm of chromosome 14 (14q32.2) and acts as an adipogenesis gatekeeper by preventing adipocyte differentiation; this factor is expressed in kisspeptin cell lines and several hypothalamic nuclei [51]

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Summary

Frontiers in Endocrinology

Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach. It is clear that a change in the pattern of pituitary gonadotropin secretion serves as a hormonal trigger for puberty induction. This change is directly guided by the hypothalamic GnRH pulse generation, a phenomenon regulated by the Kisspeptin-Neurokinin-Dynorphin (KNDy) system in the hypothalamus. This represents the kisspeptin molecule, which is crucial in augmenting GnRH secretion at puberty, whose secretion is fine-tuned by the opposing signals neurokinin B and dynorphin. The novel kisspeptin inhibitory signal MKRN3 was described, whose role in puberty initiation provided further insight into the mechanistic aspects of pubertal onset. We present the available data in the field and attempt to provide an integrated view of this unique and crucial phenomenon

INTRODUCTION
Integrated Puberty Machinery
GnRH PULSE GENERATOR
The KNDy System
INHIBITORY SIGNALS
EXTRINSIC FACTORS
ENDOCRINE DISRUPTORS
ADIPOSE TISSUE
THE GASTROINTESTINAL AXIS
ENERGY SENSING
SYNTHESIS OF DATA
Findings
CONCLUSIONS
Full Text
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