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Multiple approaches for the evaluation of connexin-43 expression and function in macrophages.
de Sousa, Júlia Costa; Santos, Stephanie Alexia Cristina Silva; Kurtenbach, Eleonora.
Afiliación
  • de Sousa JC; Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, 21941-902 Rio de Janeiro, RJ, Brazil; Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil. Electronic address: julia.sousa@bioqmed.ufrj.br.
  • Santos SACS; Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
  • Kurtenbach E; Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, 21941-902 Rio de Janeiro, RJ, Brazil; Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
J Immunol Methods ; 533: 113741, 2024 Oct.
Article en En | MEDLINE | ID: mdl-39111361
ABSTRACT
Connexins are essential gap junction proteins that play pivotal roles in intercellular communication in various organs of mammals. Connexin-43 (Cx43) is expressed in various components of the immune system, and there is extensive evidence of its participation in inflammation responses. The involvement of Cx43 in macrophage functionality involves the purinergic signaling pathway. Macrophages contribute to defenses against inflammatory reactions such as bacterial sepsis and peritonitis. Several assays can identify the presence and activity of Cx43 in macrophages. Real-time polymerase chain reaction (PCR) can measure the relative mRNA expression of Cx43, whereas western blotting can detect protein expression levels. Using immunofluorescence assays, it is possible to analyze the expression and observe the localization of Cx43 in cells or tissues. Moreover, connexin-mediated gap junction intercellular communication can be evaluated using functional assays such as microinjection of fluorescent dyes or scrape loading-dye transfer. The use of selective inhibitors contributes to this understanding and reinforces the role of connexins in various processes. Here, we discuss these methods to evaluate Cx43 and macrophage gap junctions.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Uniones Comunicantes / Conexina 43 / Macrófagos Límite: Animals / Humans Idioma: En Revista: J Immunol Methods Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Uniones Comunicantes / Conexina 43 / Macrófagos Límite: Animals / Humans Idioma: En Revista: J Immunol Methods Año: 2024 Tipo del documento: Article