Human Stem Cell Cultures from Cleft Lip/Palate Patients Show Enrichment of Transcripts Involved in Extracellular Matrix Modeling By Comparison to Controls


Autoria(s): BUENO, Daniela Franco; SUNAGA, Daniele Yumi; KOBAYASHI, Gerson Shigeru; AGUENA, Meire; RAPOSO-AMARAL, Cassio Eduardo; MASOTTI, Cibele; CRUZ, Lucas Alvizi; PEARSON, Peter Lees; PASSOS-BUENO, Maria Rita
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Nonsyndromic cleft lip and palate (NSCL/P) is a complex disease resulting from failure of fusion of facial primordia, a complex developmental process that includes the epithelial-mesenchymal transition (EMT). Detection of differential gene transcription between NSCL/P patients and control individuals offers an interesting alternative for investigating pathways involved in disease manifestation. Here we compared the transcriptome of 6 dental pulp stem cell (DPSC) cultures from NSCL/P patients and 6 controls. Eighty-seven differentially expressed genes (DEGs) were identified. The most significant putative gene network comprised 13 out of 87 DEGs of which 8 encode extracellular proteins: ACAN, COL4A1, COL4A2, GDF15, IGF2, MMP1, MMP3 and PDGFa. Through clustering analyses we also observed that MMP3, ACAN, COL4A1 and COL4A2 exhibit co-regulated expression. Interestingly, it is known that MMP3 cleavages a wide range of extracellular proteins, including the collagens IV, V, IX, X, proteoglycans, fibronectin and laminin. It is also capable of activating other MMPs. Moreover, MMP3 had previously been associated with NSCL/P. The same general pattern was observed in a further sample, confirming involvement of synchronized gene expression patterns which differed between NSCL/P patients and controls. These results show the robustness of our methodology for the detection of differentially expressed genes using the RankProd method. In conclusion, DPSCs from NSCL/P patients exhibit gene expression signatures involving genes associated with mechanisms of extracellular matrix modeling and palate EMT processes which differ from those observed in controls. This comparative approach should lead to a more rapid identification of gene networks predisposing to this complex malformation syndrome than conventional gene mapping technologies.

FAPESP/CEPID

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

Ministério da Ciência, Tecnologia e Inovação do Brasil (MCTI)

MCT

Financiadora de Estudos e Projetos (FINEP)

FINEP

Identificador

STEM CELL REVIEWS AND REPORTS, v.7, n.2, p.446-457, 2011

1550-8943

http://producao.usp.br/handle/BDPI/27548

10.1007/s12015-010-9197-3

http://dx.doi.org/10.1007/s12015-010-9197-3

Idioma(s)

eng

Publicador

SPRINGER HEIDELBERG

Relação

Stem Cell Reviews and Reports

Direitos

restrictedAccess

Copyright SPRINGER HEIDELBERG

Palavras-Chave #Nonsyndromic cleft lip and palate #Gene expression profile #Dental pulp #Stem cell #Epithelial-mesenchymal transition #Extracellular matrix #EPITHELIAL-MESENCHYMAL TRANSFORMATION #GENE-EXPRESSION #CRANIOFACIAL DEVELOPMENT #SUSCEPTIBILITY LOCUS #MICROARRAY ANALYSIS #PALATE #LIP #PALATOGENESIS #RECEPTOR #WIDE #Cell & Tissue Engineering #Cell Biology #Medicine, Research & Experimental
Tipo

article

original article

publishedVersion