Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury

Yukihiko Seki, Hisashi Kai, Rei Shibata, Tsuyoshi Nagata, Hideo Yasukawa, Akihiko Yoshimura, Tsutomu Imaizumi

Research output: Contribution to journalArticle

98 Citations (Scopus)

Abstract

In cultured vascular smooth muscle cells (VSMCs), Janus kinases (JAKs) and signal transducers and activators of transcription (STATs) are expressed constitutively and play a role in angiotensin II (Ang II)-induced intracellular signaling and proliferation. However, little is known regarding the relevance of these proteins to the process of vascular remodeling. The role of JAK and STAT proteins in vascular remodeling and their functional coupling with Ang II were examined in balloon-injured rat carotid artery. Immunoreactive Jak2, Tyk2, Stat1, and Stat3 were not detected in the intact artery. Immunohistostaining showed transient expressions of these JAKs and STATs in medial and neointimal VSMCs at days 2 and 5, respectively, with a peak at day 7 in both layers. The expressions declined to insignificant levels by day 14. Ang II type 1 receptors (AT1s) were coexpressed in the medial and neointimal VSMCs expressing Jak2 and Stat3. The Jak2 and Stat3 inductions in the injured artery were accompanied by constitutive Jak2 and Stat3 phosphorylations, which were enhanced by ex vivo Ang II stimulation via AT1. Additionally, a Jak2 inhibitor, AG490, blocked the Ang II-induced Stat3 phosphorylation. Furthermore, local treatment with AG490 inhibited constitutive Stat3 phosphorylation and neointimal VSMC replication and subsequently reduced neointima formation in the injured artery. In conclusion, JAK and STAT proteins were inducible in medial and neointimal VSMCs after vascular injury and were functionally coupled to AT1. The inductions of JAKs and STATs would be involved in the mechanisms of neointima formation after vascular injury.

Original languageEnglish
Pages (from-to)12-18
Number of pages7
JournalCirculation Research
Volume87
Issue number1
Publication statusPublished - 2000 Jul 7
Externally publishedYes

Fingerprint

Janus Kinases
Vascular System Injuries
Transducers
Vascular Smooth Muscle
Carotid Arteries
Smooth Muscle Myocytes
Angiotensin II
STAT Transcription Factors
Neointima
Arteries
Phosphorylation
Angiotensin Type 1 Receptor
Proteins

Keywords

  • Angiotensin
  • Arteries
  • Muscle, smooth
  • Remodeling
  • Signal transduction

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Seki, Y., Kai, H., Shibata, R., Nagata, T., Yasukawa, H., Yoshimura, A., & Imaizumi, T. (2000). Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury. Circulation Research, 87(1), 12-18.

Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury. / Seki, Yukihiko; Kai, Hisashi; Shibata, Rei; Nagata, Tsuyoshi; Yasukawa, Hideo; Yoshimura, Akihiko; Imaizumi, Tsutomu.

In: Circulation Research, Vol. 87, No. 1, 07.07.2000, p. 12-18.

Research output: Contribution to journalArticle

Seki, Y, Kai, H, Shibata, R, Nagata, T, Yasukawa, H, Yoshimura, A & Imaizumi, T 2000, 'Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury', Circulation Research, vol. 87, no. 1, pp. 12-18.
Seki Y, Kai H, Shibata R, Nagata T, Yasukawa H, Yoshimura A et al. Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury. Circulation Research. 2000 Jul 7;87(1):12-18.
Seki, Yukihiko ; Kai, Hisashi ; Shibata, Rei ; Nagata, Tsuyoshi ; Yasukawa, Hideo ; Yoshimura, Akihiko ; Imaizumi, Tsutomu. / Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury. In: Circulation Research. 2000 ; Vol. 87, No. 1. pp. 12-18.
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