Razvoj kaudalnog dijela zametka u mišjih mutanata splotch i truncate

doctoral thesis

• Title (english): Development of the caudal part of splotch and truncate mouse embryos
• Author: Dinko Mitrečić; MBZ: 272015
• Mentor: Srećko Gajović (mentor)
• Committee member: nije dostupno (član povjerenstva)
• Granter: University of Zagreb; School of Medicine; Zagreb
• Defense date and country: 2006-04-21, Croatia
• Scientific / art field, discipline and subdiscipline: BIOMEDICINE AND HEALTHCARE; Basic Medical Sciences
• Universal decimal classification (UDC): 61 - Medical sciences

Abstract

Razvoj kaudalnog dijela zametka kralješnjaka odvija se nakon završetka gastrulacije i nestanka primitivne pruge sekundarnim mehanizmom razvoja, tijekom kojeg strukture osnove repa nastaju od nediferenciranih stanica repnog pupoljka. Kaudalni dio zametka poremećen je u mišjih mutanata splotch i truncate. U splotch miševa mutiran je gen Pax3, što ima za posljedicu otvorenu neuralnu cijev (spina bifida) i poremećaj migracije stanica neuralnog grebena. U truncate miševa mutiran je gen Noto, gdje je poremećen razvoj notokorda. Hipoteza ovog istraživanja bila je da je fenotip mutiranih miševa splotch i truncate posljedica nepravilnog razvoja repnog pupoljka, te poremećenog sekundarnog mehanizma razvoja. Cilj rada bio je usporediti razvoj kaudalnog dijela zametka visoko srođenog soja C57Bl/6 s poremećenim razvojem mutanata splotch i truncate. Građa mišjih zametaka starih od 9 do 12,5 dana proučavana je svjetlosnom mikroskopijom serijskih polutankih rezova obojanih toluidinskim modrilom. U zamecima C57Bl/6 miševa sekundarni mehanizam razvoja obuhvaća postupnu diferencijaciju stanica repnog pupoljka, koje se dijele na moždinski tračak od kojeg nastaje sekundarna neuralna cijev, i repni tračak od kojeg nastaje notokord i repno crijevo. Poremećena neurulacija u splotch zametaka nije praćena poremećajem građe repnog pupoljka, osim u splotch zametaka starih 12,5 dana, gdje dolazi do sveobuhvatnog poremećaja razvoja osnove repa kaudalno od spine bifide. Spina bifida u splotch zametaka nastaje na prijelazu iz primarne u sekundarnu neuralnu cijev. U truncate zametaka djelomično nedostaje notokord. Diferencijacija repnog pupoljka je poremećena, te se notokord umjesto od repnog tračka odvaja od ventralne strane sekundarne neuralne cijevi. Dorzalni dio repnog tračka umjesto notokorda oblikuje dodatni lumen repnog crijeva. Nedostatak notokorda u osnovi repa povezan je s poremećajem razvoja susjednih struktura, neuralne cijevi i somita. Opisana morfogenetska zbivanja doprinose razumijevanju razvojnih poremećaja u čovjeka - spine bifide, sindroma kaudalne disgeneze i Waardenburgovog sindroma.

Abstract (english)

Development of the caudal part of vertebrate embryo occurs when gastrulation is completed and after the regression of the primitive streak. Tail structures form directly from the tail bud blastema, by secondary body development. The caudal part of the body is malformed in splotch and truncate embryos. Splotch is caused by mutation of Pax3 gene and it is characterized by the open neural tube (spina bifida) and defective neural crest migration. Truncate is mutant of Noto gene, characterized by defective development of the notochord. The hypothesis of this study was that the phenotype of splotch and truncate mutants resulted from defective tail bud and secondary body development. The aim of this work was to describe development of the caudal part of C57Bl/6 embryos and to compare it to those of splotch and truncate. Morphology of 9-12.5 days old embryos was investigated by light microscopy using semithin toluidin stained histology sections. The secondary body development in the caudal part of the mouse embryo included gradual differentiation of the tail bud. Tail bud divided and formed the medullary cord and the tail cord. The medullary cord differentiated in the neural tube and the tail cord differentiated in the notochord and the tail gut. Defective neurulation in splotch embryos was not accompanied by defective tail bud morphology, except in 12.5 days old embryos, when complete morphology of the tail, caudal from spina bifida, was disturbed. Spina bifida in splotch embryos developed at the primary and secondary neural tube boundary. In truncate embryos notochord was partially missing. Differentiation of the tail bud was disturbed and the notochord did not develop from the tail cord, but from ventral neuroectoderm. Dorsal part of the tail cord, instead of the notochord, formed additional tail gut. Lack of the notochord was accompanied by disturbed development of the neighboring structures, the neural tube and the somites. Described morphogenetic processes which lead to secondary neural tube and notochord malformations contribute to understanding of human birth defects – spina bifida, caudal disgenesis syndrome and Waardenburg syndrome.

• Keywords: medicina
• Keywords (english): medicine
• Language: croatian
• URN:NBN: urn:nbn:hr:105:324494
• Study programme: Title: Biomedicine and Health Sciences; Study programme type: university; Study level: postgraduate; Academic / professional title: doktor/doktorica znanosti, područje biomedicine i zdravstva (doktor/doktorica znanosti, područje biomedicine i zdravstva)
• Type of resource: Text
• Extent: 118 str.
• File origin: Born digital
• Access conditions: Open access
• Created on: 2023-05-05 07:02:24