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Morphological, biochemical and molecular evaluation of the elastogenesis in the adult tissues of the mouse pubic symphysis during and after pregnancy

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Author(s):
Sílvio Roberto Consonni
Total Authors: 1
Document type: Master's Dissertation
Press: Campinas, SP.
Institution: Universidade Estadual de Campinas (UNICAMP). Instituto de Biologia
Defense date:
Examining board members:
Paulo Pinto Joazeiro; Lucia Elvira Alvares; Olga Maria de Toledo Correa
Advisor: Paulo Pinto Joazeiro; Claudio Chrysostomo Werneck
Abstract

The organization of elastic fibers involves the synthesis and the deposition of molecules in a high regulated sequence to ensure the elastic characteristics in the early stages of development. During pregnancy, elastic fibers-enriched pelvic tissues change to allow safe delivery and this remodeling is essential to the vaginal delivery. The mouse pubic symphysis articulation also remodels in a controlled hormonal process. This phenomenon comprises the "transformation" of the fibrocartilage into an interpubic ligament (IpL) followed by its relaxation before parturition. After the first parturition, recovery process occurs to ensure the pelvic tissue homeostasis. Adding to that, pelvic organ support impairment had been described in genetically modified mouse for the proteins involved in the elastogenesis such as lysyl oxidase-like 1 (LOXL-1), fibulin-3 and -5. Since, ligaments are the main supportive structures of pelvic organs, the aim of this study was to evaluate the elastogenesis in the IpL development during mouse pregnancy. Thus virgin, pregnant and postpartum C57Bl/06 wild-type and fibrillin-1mg?/+ female mice were studied using light, confocal, transmission electron microscopy, western blotting and real-time PCR. Both, wild-type and fibrillin-1mg?/+ female mice showed classically the separation of the pubic bones, the formation and relaxation of the IpL and the recovery at postpartum. These processes suggested a pattern which cells control the extracellular matrix remodeling under hormonal and molecular signaling. The ultra-structure of the fibrocartilaginous tissue had slender bundles of microfibrils randomly distributed among the fibrochondrocytes. By the time IpL is formed, there were seen elastic fibers, which consist of small conglomerates of amorphous material, distributed among the bundles of microfibrils. The IpL showed elastic fibers and all tissue compounds aligned to the opening axis of the articulation before parturition. The immunohistochemical study and quantitative gene expression indicated that during IpL development in wild-type mice, tropoelastin/elastin, fibrillin-1, fibrillin-2, LOXL-1, fibulin-5 and TGF-? were spatial and temporal regulated, and these molecules might contribute to the synthesis of new elastic fibers that assure the elasticity that is needed to the pelvic girdle during preparation for parturition and also the recovery at postpartum. However, compared to wild-type mice, alterations were found in the quantitative gene expression of elastin, fibrillin-1, LOXL-1, fibulin-5 and TGF- ?, different from the morphology that was very similar to the one that was observed in wild-type mice. In this study, the fibrillinmg?/+ mice did not show pelvic organ prolapse after the first parturition as LOXL1-/- did (Liu et al., 2004), neither morphological modifications that could be related to the weakness of pelvic tissue. However, this is the first work about pelvic dysfunctions in multiparous fibrillin-1mg?/+ mice used as reproductive matrices. In conclusion, the elastic fiber assembly that occurred in the mouse pubic symphysis during the adult life has characteristics of a model that could be used to understand normal and pathological processes, mainly those related to genetically modified mice for the proteins involved in the elastogenesis. Then, this work may bring readers up-to-date with accumulating evidence that the mouse pubic symphysis undergoes remarkable modifications during pregnancy with new synthesized elastic fibers and may contribute to our understanding of the biological mechanisms about elastic fiber assembly (AU)