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Ann Anat ; 200: 24-9, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25723517

RESUMO

There have been few studies on human embryos describing a specific pattern of hindgut colonization by hematopoietic stem cells (HSCs) and interstitial Cajal cells (ICCs). We aimed to study CD34, CD45 and CD117/c-kit expression in late stage human embryos, to attain observational data that could be related to studies on the aorta-gonad-mesonephros (AGM)-derived HSCs, and data on hindgut ICCs. Antibodies were also applied to identify alpha-smooth muscle actin and neurofilaments. Six human embryos of 48-56 days were used. In the 48 day embryo, the hindgut was sporadically populated by c-kit+ ICCs, but, in all other embryos, a layer of myenteric ICCs had been established. Intraneural c-kit+ cells were found in pelvic nerves and vagal trunks, suggesting that the theory of Ramon y Cajal assuming that ICCs may be primitive neurons may not be so invalid. Also in the 48 day embryo, c-kit+/CD45+ perivascular cells were found along the pelvic neurovascular axes, suggesting that not only liver, but also other organs could be seeded with HSCs from the AGM region. CD45+ cells with dendritic morphologies were found in all hindgut layers, including the epithelium. This last evidence is suggestive of an AGM contribution to the tissue resident macrophages and could be related to processes of sprouting angiogenesis which, in turn, have been found to be guided by filopodia of endothelial tip cells. Further studies on human embryonic and fetal material should be performed to attempt to clarify whether the hindgut colonization with HSCs is a transitory or definitive process.


Assuntos
Células-Tronco Embrionárias/fisiologia , Feto/fisiologia , Trato Gastrointestinal/citologia , Células-Tronco Hematopoéticas/fisiologia , Células Intersticiais de Cajal/fisiologia , Actinas/metabolismo , Adulto , Células Dendríticas/fisiologia , Feminino , Feto/citologia , Trato Gastrointestinal/embriologia , Trato Gastrointestinal/fisiologia , Humanos , Antígenos Comuns de Leucócito/metabolismo , Plexo Mientérico/citologia , Plexo Mientérico/embriologia , Neovascularização Fisiológica/fisiologia , Gravidez , Proteínas Proto-Oncogênicas c-kit/genética , Proteínas Proto-Oncogênicas c-kit/metabolismo
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