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Quantification of Immunostained Caspase-9 in Retinal Tissue.
Colón Ortiz, Crystal K; Potenski, Anna M; Johnson, Kendra V; Chen, Claire W; Snipas, Scott J; Jean, Ying Y; Avrutsky, Maria I; Troy, Carol M.
Afiliación
  • Colón Ortiz CK; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Potenski AM; Department of Molecular Pharmacology and Therapeutics, Vagelos College of Physicians and Surgeons, Columbia University.
  • Johnson KV; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Chen CW; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Snipas SJ; NCI-designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute.
  • Jean YY; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Avrutsky MI; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Troy CM; Department of Pathology & Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University; Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University; The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Vagelos College of Physic
J Vis Exp ; (185)2022 07 25.
Article en En | MEDLINE | ID: mdl-35938825
ABSTRACT
The family of caspases is known to mediate many cellular pathways beyond cell death, including cell differentiation, axonal pathfinding, and proliferation. Since the identification of the family of cell death proteases, there has been a search for tools to identify and expand the function of specific family members in development, health, and disease states. However, many of the currently commercially available caspase tools that are widely used are not specific for the targeted caspase. In this report, we delineate the approach we have used to identify, validate, and target caspase-9 in the nervous system using a novel inhibitor and genetic approaches with immunohistochemical read-outs. Specifically, we used the retinal neuronal tissue as a model to identify and validate the presence and function of caspases. This approach enables the interrogation of cell-type specific apoptotic and non-apoptotic caspase-9 functions and can be applied to other complex tissues and caspases of interest. Understanding the functions of caspases can help to expand current knowledge in cell biology, and can also be advantageous to identify potential therapeutic targets due to their involvement in disease.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retina / Caspasas Tipo de estudio: Prognostic_studies Idioma: En Revista: J Vis Exp Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retina / Caspasas Tipo de estudio: Prognostic_studies Idioma: En Revista: J Vis Exp Año: 2022 Tipo del documento: Article
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