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We began analyzing https://journals.biologists.com/jcs/article-abstract/109/2/387/24728/CD36-participates-in-the-phagocytosis-of-rod-outer?redirectedFrom=fulltext, but it redirected us to https://journals.biologists.com/jcs/article-abstract/109/2/387/24728/CD36-participates-in-the-phagocytosis-of-rod-outer?redirectedFrom=fulltext. The analysis below is for the second page.

Title[redir]:
CD36 participates in the phagocytosis of rod outer segments by retinal pigment epithelium | Journal of Cell Science | The Company of Biologists
Description:
ABSTRACT. Mechanisms of phagocytosis are complex and incompletely understood. The retinal pigment epithelium provides an ideal system to study the specific aspects of phagocytosis since an important function of this cell is the ingestion of packets of membranous discs that are normally discarded at the apical ends of rod and cone cells during outer segment renewal. Here we provide evidence that rod outer segment phagocytosis by retinal pigment epithelium is mediated by CD36, a transmembrane glycoprotein which has been previously characterized on hematopoietic cells as a receptor for apoptotic neutrophils and oxidized low density lipoprotein.Immunocytochemical staining with monoclonal and polyclonal antibodies demonstrated CD36 expression by both human and rat retinal pigment epithelium in transverse cryostat sections of normal retina and in primary cultured cells. By western blot analysis of retinal pigment epithelial cell lysates, polyclonal and monoclonal antibodies to CD36 recognized an 88 kDa protein which comigrated with platelet CD36. Furthermore, the synthesis of CD36 mRNA by retinal pigment epithelium was confirmed by reverse transcriptase-PCR using specific CD36 oligonucleotides. The addition of CD36 antibodies to cultured retinal pigment epithelial cells reduced the binding and internalization of 125I-labeled rod outer segments by 60%. Immunofluorescence confocal microscopy confirmed that outer segment uptake was significantly diminished by an antibody to CD36.Moreover, we found that transfection of a human melanoma cell line with CD36 cDNA enabled these cells to bind and internalize isolated photoreceptor outer segments as seen by double immunofluorescent staining for surface bound and total cell-associated rod outer segments, and by measurement of cell-associated 125I-labeled rod outer segments.We conclude that the multifunctional scavenger receptor CD36 participates in the clearance of photoreceptor outer segments by retinal pigment epithelium and thus, participates in the visual process.

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Keywords {πŸ”}

cell, open, outer, retinal, pigment, menu, article, journal, rod, epithelium, biology, search, sign, segments, cells, company, register, issue, phagocytosis, segment, alert, content, contacts, participates, icon, mechanisms, provide, antibodies, microscopy, biologists, jcs, decision, manuscript, imaging, mitochondrial, policy, registered, skip, input, journals, science, articles, february, author, information, versions, share, tools, specific, aspects,

Topics {βœ’οΈ}

open menu article research article cell science journal fast-tracked decision making jcs fast-track option photoreceptor outer segments rod outer segments retinal pigment epithelium rod outer segment primary cultured cells outer segment renewal outer segment uptake journals journal article information search transverse cryostat sections western blot analysis reverse transcriptase-pcr google scholar crossref cambridge cb24 9lf cd36 cdna enabled double immunofluorescent staining guest editors ana οΏ½cell biology cell biology specific cd36 oligonucleotides prokaryotic intracytoplasmic membranes company limited skip view access $30 institution sign permissions sign rights reserved company special issue cd36 antibodies manuscripts cell sci total cell content register cone cells hematopoietic cells colleagues provide decision letters initial decision immunocytochemical staining monoclonal antibodies cd36 recognized platelet cd36

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ScholarlyArticle:
      context:https://schema.org
      id:https://journals.biologists.com/jcs/article/109/2/387/24728/CD36-participates-in-the-phagocytosis-of-rod-outer
      name:CD36 participates in the phagocytosis of rod outer segments by retinal pigment epithelium
      datePublished:1996-02-01
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         datePublished:1996-02-01
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            id:https://journals.biologists.com/jcs
            type:Periodical
            name:Journal of Cell Science
            issn:
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      url:https://dx.doi.org/10.1242/jcs.109.2.387
      keywords:
         CD36
         Rod outer segment
         Retinal pigment epithelium
      inLanguage:en
      copyrightHolder:
      copyrightYear:2025
      publisher:
      author:
            name:Ryeom, Sandra W.
            affiliation:1 Program in Cell Biology and Genetics, Division of Hematology-Oncology and NIH-Specialized Center of Thrombosis Research
            type:Person
            name:Sparrow, Janet R.
            affiliation:2 Department of Ophthalmology , Cornell University Medical College , New York, NY 10021, USA
            type:Person
            name:Silverstein, Roy L.
            affiliation:1 Program in Cell Biology and Genetics, Division of Hematology-Oncology and NIH-Specialized Center of Thrombosis Research
            type:Person
      description:ABSTRACT. Mechanisms of phagocytosis are complex and incompletely understood. The retinal pigment epithelium provides an ideal system to study the specific aspects of phagocytosis since an important function of this cell is the ingestion of packets of membranous discs that are normally discarded at the apical ends of rod and cone cells during outer segment renewal. Here we provide evidence that rod outer segment phagocytosis by retinal pigment epithelium is mediated by CD36, a transmembrane glycoprotein which has been previously characterized on hematopoietic cells as a receptor for apoptotic neutrophils and oxidized low density lipoprotein.Immunocytochemical staining with monoclonal and polyclonal antibodies demonstrated CD36 expression by both human and rat retinal pigment epithelium in transverse cryostat sections of normal retina and in primary cultured cells. By western blot analysis of retinal pigment epithelial cell lysates, polyclonal and monoclonal antibodies to CD36 recognized an 88 kDa protein which comigrated with platelet CD36. Furthermore, the synthesis of CD36 mRNA by retinal pigment epithelium was confirmed by reverse transcriptase-PCR using specific CD36 oligonucleotides. The addition of CD36 antibodies to cultured retinal pigment epithelial cells reduced the binding and internalization of 125I-labeled rod outer segments by 60%. Immunofluorescence confocal microscopy confirmed that outer segment uptake was significantly diminished by an antibody to CD36.Moreover, we found that transfection of a human melanoma cell line with CD36 cDNA enabled these cells to bind and internalize isolated photoreceptor outer segments as seen by double immunofluorescent staining for surface bound and total cell-associated rod outer segments, and by measurement of cell-associated 125I-labeled rod outer segments.We conclude that the multifunctional scavenger receptor CD36 participates in the clearance of photoreceptor outer segments by retinal pigment epithelium and thus, participates in the visual process.
      pageStart:387
      pageEnd:395
      siteName:The Company of Biologists
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      headline:CD36 participates in the phagocytosis of rod outer segments by retinal pigment epithelium
      image:https://cob.silverchair-cdn.com/cob/content_public/journal/jcs/issue/109/2/6/m_joces_109_2.cover.png?Expires=1814644676&Signature=IOf5L7OczfuuRmKuYY-W8srUS5Sb8N5uQ0Ppr8qCOtd67NEYBy0REbh8Iq163PFuCzlSwUXwbOyYHgkbcdgUioDMJk0LPpzo8dFZ-sApT3YOp9llq1UMb5IHm8uZTgbhl7VUX3HJN1A~8w1EX9Kkgoc7iPYLrcn-Ao3yYsDbjjPb4aoxvMQ36~CBWqlVYTCS7xS65ZRe28k1Rx-swxeWt7RwDxuMkoJXbcap4kPY8JL-WdvCRhAD0mBsO68mDvZr-DfpcM5aibIYQcn~3M9uyqlTjrKReyMAhVAFrQDhXtSiyn~FXi3nZof6IFbUxC9a6nWF3c1KfJc~kAAZy3gGKw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA
      image:alt:Issue Cover
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PublicationIssue:
      id:https://journals.biologists.com/jcs/issue/109/2
      issueNumber:2
      datePublished:1996-02-01
      isPartOf:
         id:https://journals.biologists.com/jcs
         type:Periodical
         name:Journal of Cell Science
         issn:
            1477-9137
Periodical:
      id:https://journals.biologists.com/jcs
      name:Journal of Cell Science
      issn:
         1477-9137
Person:
      name:Ryeom, Sandra W.
      affiliation:1 Program in Cell Biology and Genetics, Division of Hematology-Oncology and NIH-Specialized Center of Thrombosis Research
      name:Sparrow, Janet R.
      affiliation:2 Department of Ophthalmology , Cornell University Medical College , New York, NY 10021, USA
      name:Silverstein, Roy L.
      affiliation:1 Program in Cell Biology and Genetics, Division of Hematology-Oncology and NIH-Specialized Center of Thrombosis Research

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