Co-localization of nestin and insulin and expression of islet cell markers in long-term human pancreatic nestin-positive cell cultures

• Autor(a) principal: Maria-Engler, Sylvia Stucchi
• Data de Publicação: 2004
• Outros Autores: Correa-Giannella, Maria Lucia C, Labriola, Leticia, Krogh, Karin, Colin, Christian, Lojudice, Fernando Henrique, Aita, Carlos Alberto Mayora, Oliveira, Elizabeth Maria Costa de, Correa, Tatiana C Silveira, Silva, Irenice Cairo da, Genzini, Tercio, Miranda, Marcelo Perosa de, Noronha, Irene Lourdes, Vilela, Luciano, Coimbra, Cassio Negro, Mortara, Renato A. [UNIFESP], Guia, Marcos Mares, Eliaschewitz, Freddy Goldenberg, Sogayar, Mari Cleide
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• Texto Completo: http://dx.doi.org/10.1677/joe.1.05703; http://repositorio.unifesp.br/handle/11600/28032

Strategies to differentiate progenitor cells into beta cells in vitro have been considered as an alternative to increase beta cell availability prior to transplantation. It has recently been suggested that nestin-positive cells could be multipotential stern cells capable of expressing endocrine markers upon specific stimulation; however, this issue still remains controversial. Here, we characterized short- and long-term islet cell cultures derived from three different human islet preparations. with respect to expression of nestin and islet cell markers, using confocal microscopy and semi-quantitative PT-PCR. the number of nestin-positive cells was found to be strikingly high in long-term cultures. in addition, a large proportion (49.7%) of these nestin-positive cells, present in long-term culture, are shown to be proliferative, as judged by BrdU incorporation. the proportion of insulin-positive cells was found to be high in short-term (up to 28 days) cultures and declined thereafter, when cells were maintained in the presence of 10% serum, concomitantly with the decrease in insulin and PDX-1 expression. Interestingly, insulin and nestin co-expression was observed as a rare event in a small proportion of cells present in freshly isolated human islets as well as in purified islet cells cultured in vitro for long periods of time. in addition, upon long-term subculturing of nestin-positive cells in 10% serum, we observed reappearance of insulin expression at the mRNA level; when these cultures were shifted to 1% serum for a month, expression of insulin, glucagon and somatostatin was also detected, indicating that manipulating the culture conditions can be used to modulate the nestin-positive cell's fate. Attempts to induce cell differentiation by plating nestin-positive cells onto Matrigel revealed that these cells tend to aggregate to form islet-like clusters, but this is not sufficient to increase insulin expression upon short-term culture. Our data corroborate previous findings indicating that, at least ill vitro, nestin-positive cells may undergo the early stages of differentiation to an islet cell phenotype and that long-term cultures of nestin-positive human islet cells may be considered as a potential source of precursor cells to generate fully differentiated/functional beta cells.