<?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>S0535-51332023000300267</article-id>
<article-id pub-id-type="doi">10.54817/ic.v64n3a01</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Induced differentiation of adipose-derived stem cells enhance secretion of neurotrophic factors.]]></article-title>
<article-title xml:lang="es"><![CDATA[La diferenciación inducida de las células madre derivadas del tejido adiposo aumenta la secreción de factores neurotróficos.]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zeng]]></surname>
<given-names><![CDATA[Xin]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Liu]]></surname>
<given-names><![CDATA[Ya-nan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[Zhen]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[He]]></surname>
<given-names><![CDATA[Yun]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[Fang]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[Shu-yuan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gu]]></surname>
<given-names><![CDATA[Jing]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lu]]></surname>
<given-names><![CDATA[Li]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Lanzhou University School of Basic Medical Sciences ]]></institution>
<addr-line><![CDATA[Lanzhou Gansu]]></addr-line>
<country>China</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Lanzhou University The First Clinical Medical College ]]></institution>
<addr-line><![CDATA[Lanzhou Gansu]]></addr-line>
<country>China</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Gansu University of Traditional Chinese Medicine  ]]></institution>
<addr-line><![CDATA[Lanzhou Gansu]]></addr-line>
<country>China</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2023</year>
</pub-date>
<volume>64</volume>
<numero>3</numero>
<fpage>267</fpage>
<lpage>280</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_arttext&amp;pid=S0535-51332023000300267&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_abstract&amp;pid=S0535-51332023000300267&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_pdf&amp;pid=S0535-51332023000300267&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Adipose-derived stem cells (ADSCs) could be ideal seed cells for repairing nerve injury as they have the potential for multidirectional differentiation. However, it is still unclear whether the undifferentiated or the differentiated ADSCs have priorities in promoting axonal regeneration and myelin formation. In this study, the primary ADSCs from rats were cultured and differentiated. The morphology, differentiation potential, and secretion of neu rotrophic factors of ADSCs were compared before and after induction. Undifferentiated ADSCs (uADSCs) were aggregated into bundles containing reticular, star, and polygonal structures. They contained a large number of lipid droplets and were positive for Oil red O staining. After differentiation, differentiation ADSCs (dADSCs) become long and spindle-shaped with decreasing protrusions around the cells, spiraling growth, and were negative for Oil red O staining. When comparing the groups the flow cytometer analysis showed: similar CD29 and CD45 surface markers in both groups; and CD44 and CD90 markers were very low in the undifferentiated groups. The levels of neurotrophin 3 (NT-3) and neuregulin 1 (NRG-1), and their receptors tropomyosin receptor kinase C (TrkC) and receptor protein-tyrosine kinase erbB-4 (ErbB-4) in dADSCs were higher than those in uADSCs. While the expressions of myelin protein zero (P0), myelin-associated glycoprotein (MAG), and purine receptor P2X7 (P2X7) were not significantly different before and after differentiation. It may be speculated that the dADSCs have enhanced abilities in nerve repairment which is associated with increased expression of neurotrophic factors.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Las células madre derivadas del tejido adiposo (ADSCs) podrían ser una semilla ideal de células para la reparación de lesiones nerviosas, ya que tienen el potencial de diferenciación multidireccional. Sin embargo, aún no está claro si las ADSCs indiferenciadas o diferenciadas tienen prioridades en la promoción de la regeneración axonal y la formación de mielina. En este estudio, ADSCs primarias de las ratas fueron cultivadas y diferenciadas. Se compararon la morfología, el potencial de diferenciación y la secreción de los factores neurotróficos de las ADSCs antes y después de la inducción. Las ADSCs indiferenciadas (uADSCs) se encontraban agregadas en haces que contenían estructuras reticulares, estrelladas y poligonales. Contenían un gran número de gotitas de lípidos y fueron positivas para la tinción de Aceite Rojo O. Después de la diferenciación, las ADSCs (dADSCs) se vuelven largas y en forma de huso con un número decreciente de protuberancias alrededor de las células, crecimiento en espiral, y fueron negativas para la tinción de Aceite Rojo O. Cuando se compararon los dos grupos, análisis del citómetro de flojo muestra que los dos grupos de marcadores superficiales CD29 y CD45 eran similares; y los marcadores CD44 y CD90 eran muy bajos en el grupo indiferenciado. Los niveles de neurotrofina 3 (NT-3) y neuregulina 1 (NRG-1) y sus receptores, el receptor de tropomiosina quinasa C (TrkC) y el receptor de proteína tirosina quinasa erbB- 4 (ErbB-4) en dADSC fueron más altos que los de uADSC. Mientras que las expresiones de proteína cero de mielina (P0), glicoproteína asociada a mielina (MAG) y receptor de purina P2X7 (P2X7) no fueron significativamente diferentes antes y después de la diferenciación. Se puede especular que las dADSC tienen capacidades mejoradas en la reparación nerviosa que se asocia con una mayor expresión de factores neurotróficos.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[differentiated ADSCs]]></kwd>
<kwd lng="en"><![CDATA[Schwann cells]]></kwd>
<kwd lng="en"><![CDATA[neurotrophic factors]]></kwd>
<kwd lng="en"><![CDATA[P2X7]]></kwd>
<kwd lng="en"><![CDATA[nerve damage]]></kwd>
<kwd lng="es"><![CDATA[ADSC diferenciadas]]></kwd>
<kwd lng="es"><![CDATA[células de Schwann]]></kwd>
<kwd lng="es"><![CDATA[factores neurotróficos]]></kwd>
<kwd lng="es"><![CDATA[P2X7]]></kwd>
<kwd lng="es"><![CDATA[daño nervioso]]></kwd>
</kwd-group>
</article-meta>
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