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1.
Exp Eye Res ; 87(2): 115-21, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18571648

RESUMO

The corneal epithelium is continuously being renewed. Differentiated epithelial cells originate from limbal stem cells (LSCs) located in the periphery of the cornea, the corneoscleral limbus. We have recently identified superoxide dismutase 2 (SOD2) and cytokeratin (CK) 15 as limbal basal cell markers and potential markers for LSCs and early transient amplifying cells in human adults. In this study, we describe the development of the ectodermally derived LSCs and the mesodermally derived niche cells from the time at which the cornea is defined (week 6) until the formation of the early limbal niche (week 14) in human embryos and fetuses. The expression of SOD2 and CK15 was investigated together with other recently identified limbal proteins. Previously suggested LSC and differentiation markers (PAX6, aquaporin-1 and nestin) were also investigated. Both SOD2 and CK15 were present in the corneal epithelium from week 6. However, in week 14 they were predominantly expressed in the limbal epithelium. Both proteins were expressed already from week 7 in a stromal triangular region from which the early mesodermal limbal niche most likely originates. PAX6 was expressed in both ectodermally and mesodermally derived parts of the limbal niche, underscoring the importance of PAX6 in niche formation.


Assuntos
Proteínas do Olho/metabolismo , Células-Tronco Fetais/metabolismo , Limbo da Córnea/embriologia , Aquaporina 1/metabolismo , Biomarcadores/metabolismo , Diferenciação Celular , Epitélio Corneano/citologia , Epitélio Corneano/embriologia , Epitélio Corneano/metabolismo , Desenvolvimento Fetal/fisiologia , Células-Tronco Fetais/citologia , Proteínas de Homeodomínio/metabolismo , Humanos , Técnicas Imunoenzimáticas , Proteínas de Filamentos Intermediários/metabolismo , Queratina-15/metabolismo , Limbo da Córnea/citologia , Limbo da Córnea/metabolismo , Proteínas do Tecido Nervoso/metabolismo , Nestina , Fator de Transcrição PAX6 , Fatores de Transcrição Box Pareados/metabolismo , Proteínas Repressoras/metabolismo , Superóxido Dismutase/metabolismo
2.
J Histochem Cytochem ; 55(12): 1213-28, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17712177

RESUMO

YKL-40 is a growth factor for chondrocytes and fibroblasts. The aim was to evaluate YKL-40 expression in the musculoskeletal system during early human development. We studied sections from 15 human embryos [weeks 5.5-8; 7- to 31-mm crown-rump length (CRL)] and 68 fetuses (weeks 9-14; 33- to 105-mm CRL) for YKL-40 protein expression by immunohistochemistry. YKL-40 mRNA expression was evaluated in two human embryos (days 41 and 51). Initially YKL-40 is expressed in all germ layers: ecto-, meso-, and endoderm. YKL-40 mRNA and protein expression are found in tissues of the ecto-, meso-, and endoderm, and YKL-40 protein expression is present during development of cartilage, bone, joints, and muscles. At the cellular level, YKL-40 protein expression is high in tissues characterized by rapid proliferation, marked differentiation, and undergoing morphogenetic changes. Examples of rapid cell proliferation include the chondrogenic inner layer of perichondrium and the osteogenic inner layer of periosteum. Differences in YKL-40 expression during differentiation are found in the chondrogenic and osteogenic cell lineages. The initial shaping of cartilage and bone models and joints is concomitant with a strong outline of YKL-40-positive cells. This indicates that YKL-40 is associated with cell proliferation, differentiation, and tissue morphogenesis during development of the human musculoskeletal system.


Assuntos
Glicoproteínas/biossíntese , Sistema Musculoesquelético/metabolismo , Adipocinas , Proteína 1 Semelhante à Quitinase-3 , Idade Gestacional , Glicoproteínas/genética , Humanos , Imuno-Histoquímica , Lectinas , Sistema Musculoesquelético/embriologia , Especificidade de Órgãos , RNA Mensageiro/biossíntese , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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