<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0535-5133</journal-id>
<journal-title><![CDATA[Investigación Clínica]]></journal-title>
<abbrev-journal-title><![CDATA[Invest. clín]]></abbrev-journal-title>
<issn>0535-5133</issn>
<publisher>
<publisher-name><![CDATA[Instituto de Investigaciones Clínicas "Dr. Américo Negrette", Facultad de Medicina, Universidad del Zulia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0535-51332024000200179</article-id>
<article-id pub-id-type="doi">10.54817/ic.v65n2a05</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Insulin-like growth factor-1 promotes the proliferation and odontogenic differentiation of human dental pulp cells in vitro and in vivo.]]></article-title>
<article-title xml:lang="es"><![CDATA[El factor de crecimiento similar a la insulina-1 promueve la proliferación y diferenciación odontogénica de células de pulpa dental humana in vitro e in vivo.]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[Yan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Du]]></surname>
<given-names><![CDATA[Nan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Liu]]></surname>
<given-names><![CDATA[Cong-na]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[Wen-jing]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,The Second Hospital of Hebei Medical University Department of Oral Medicine ]]></institution>
<addr-line><![CDATA[Shijiazhuang ]]></addr-line>
<country>China</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2024</year>
</pub-date>
<volume>65</volume>
<numero>2</numero>
<fpage>179</fpage>
<lpage>191</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_arttext&amp;pid=S0535-51332024000200179&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_abstract&amp;pid=S0535-51332024000200179&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_pdf&amp;pid=S0535-51332024000200179&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Human dental pulp cells (hDPCs) have emerged as a potential alternative for the regeneration of dental tissues. Insulin-like growth factor-1 (IGF-1) is involved in the proliferation and osteogenic differentiation of hDPCs in vitro. However, the effect of IGF-1 on the proliferation and odontogenic differentiation of hDPCs in vivo remains unknown. This study collected hDPCs from healthy premolars and third molars by collagenase type I and dispase. Immunocytochemical staining showed positive vimentin staining and negative cytokeratin staining in hDPCs. Treatment with IGF-1 (50, 75, and 100 ng/mL) significantly increased the proliferation ability of hDPCs in a concentration-dependent manner. In vivo experiments, hDPCs were seeded into an acellular dermal matrix and transplanted subcutaneously into nude mice. After two and four weeks of transplantation, the hematoxylin and eosin staining revealed more cells and extracellular matrix in implants from the IGF-1 treatment group, and Alizarin Red staining revealed more mineralized tissue compared to the control group. Transmission electron microscopy (TEM) analysis of hDPCs showed an abundance of mitochondria, rough endoplasmic reticulum, and Golgi complexes. In conclusion, IGF-1 promotes the proliferation of hDPCs in vitro and odontogenic differentiation of hDPCs in vivo, indicating that modifying IGF-1 signaling may provide potential strategies for the regeneration of dental tissues.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Las células de la pulpa dental humana (hDPCs) han emergido como una alternativa prometedora para la regeneración de tejidos dentales. El factor de crecimiento insulínico tipo 1 (IGF-1) juega un rol crucial en la proliferación y diferenciación osteogénica de las hDPCs en condiciones in vitro. No obstante, el impacto del IGF-1 sobre la proliferación y diferenciación odontogénica de las hDPCs en un contexto in vivo aún no ha sido completamente elucidado. En el presente estudio, se extrajeron hDPCs de premolares y terceros molares sanos mediante el uso de colagenasa tipo I y dispasa. La tinción inmunocitoquímica de las hDPCs reveló una reactividad positiva para vimentina y negativa para citoqueratina. El tratamiento con IGF-1 en concentraciones de 50, 75 y 100 ng/mL incrementó de manera significativa y dependiente de la dosis la capacidad proliferativa de las hDPCs. En experimentos in vivo, las hDPCs fueron implantadas en una matriz dérmica acelular y posteriormente trasplantadas de manera subcutánea en ratones desnudos. Tras 2 y 4 semanas de trasplante, la coloración con hematoxilina y eosina evidenció un aumento en la cantidad de células y matriz extracelular en los implantes tratados con IGF-1, mientras que la coloración con Rojo de Alizarina indicó una mayor formación de tejido mineralizado en comparación con el grupo control. El análisis mediante microscopía electrónica de transmisión (TEM) de las hDPCs mostró una abundante presencia de mitocondrias, retículo endoplásmico rugoso y complejos de Golgi. En conclusión, nuestros hallazgos sugieren que el IGF-1 favorece la proliferación de las hDPCs in vitro así como su diferenciación odontogénica in vivo, lo cual señala que la modificación de la señalización del IGF-1 podría ofrecer estrategias potenciales para la regeneración de tejidos dentales.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[dental tissue regeneration]]></kwd>
<kwd lng="en"><![CDATA[odontoblasts]]></kwd>
<kwd lng="en"><![CDATA[osteogenic differentiation]]></kwd>
<kwd lng="es"><![CDATA[regeneración del tejido dental]]></kwd>
<kwd lng="es"><![CDATA[odontoblastos]]></kwd>
<kwd lng="es"><![CDATA[diferenciación osteogénica]]></kwd>
</kwd-group>
</article-meta>
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