Immunocytochemical demonstration of a new vimentin-associated protein in 3T3 fibroblasts

Seu Mei Wang, Jin-Shan Chen, Tsorng Harn Fong, Jiahn Chun Wu

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Using a xanthophore cytoskeletal preparation as immunogen, we have produced a monoclonal antibody, A2, which recognized a 160 kDa protein in 3T3 fibroblasts. This protein makes up a cytoplasmic filamentous system, which colocalizes with vimentin filaments. When microtubules and actin filaments are dissolved by high salt extraction, staining with antibody A2 is unaffected. Immunoblot analysis confirms that the 160 kDa protein is co-isolated with vimentin during in vivo high salt extraction. Following vinblastine treatment, both the 160 kDa protein and vimentin become localized to perinuclear caps, as do other intermediate filaments and their associated proteins; after vinblastine removal, the immunostaining produced by A2 becomes filamentous. Immunoelectron microscopy demonstrates that antibody A2 stains a filament system with a diameter of about 10 nm. Our observations suggest that the 160 kDa protein may be a new vimentin-associated protein which differs from the intermediate filament-associated proteins previously reported, and is widely distributed in several cell types.

Original languageEnglish
Pages (from-to)469-476
Number of pages8
JournalHistochemical Journal
Volume28
Issue number7
DOIs
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Anatomy
  • Cell Biology

Fingerprint

Dive into the research topics of 'Immunocytochemical demonstration of a new vimentin-associated protein in 3T3 fibroblasts'. Together they form a unique fingerprint.

Cite this