Hyaluronan-Induced CD44-iASPP Interaction Affects Fibroblast Migration and Survival

Author:

Lin Chun-Yu12ORCID,Basu Kaustuv13,Ruusala Aino1,Kozlova Inna1,Li Yan-Shuang14ORCID,Skandalis Spyridon S.15,Heldin Carl-Henrik1ORCID,Heldin Paraskevi1ORCID

Affiliation:

1. Department of Medical Biochemistry and Microbiology, Uppsala University, SE-751 23 Uppsala, Sweden

2. Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University Hospital, School of Medicine, College of Medicine, Center for Tropical Medicine and Infectious Diseases Research, Kaohsiung Medical University, Kaohsiung 807, Taiwan

3. Department of Mechanical Engineering, McGill University, Montréal, QC H3A 0C3, Canada

4. Department of Breast Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China

5. Laboratory of Biochemistry, Department of Chemistry, University of Patras, 26504 Patras, Greece

Abstract

In the present study, we show that the inhibitor of the apoptosis-stimulating protein of p53 (iASPP) physically interacts with the hyaluronan receptor CD44 in normal and transformed cells. We noticed that the CD44 standard isoform (CD44s), but not the variant isoform (CD44v), bound to iASPP via the ankyrin-binding domain in CD44s. The formation of iASPP-CD44s complexes was promoted by hyaluronan stimulation in fibroblasts but not in epithelial cells. The cellular level of p53 affected the amount of the iASPP-CD44 complex. iASPP was required for hyaluronan-induced CD44-dependent migration and adhesion of fibroblasts. Of note, CD44 altered the sub-cellular localization of the iASPP-p53 complex; thus, ablation of CD44 promoted translocation of iASPP from the nucleus to the cytoplasm, resulting in increased formation of a cytoplasmic iASPP-p53 complex in fibroblasts. Overexpression of iASPP decreased, but CD44 increased the level of intracellular reactive oxygen species (ROS). Knock-down of CD44s, in the presence of p53, led to increased cell growth and cell density of fibroblasts by suppression of p27 and p53. Our observations suggest that the balance of iASPP-CD44 and iASPP-p53 complexes affect the survival and migration of fibroblasts.

Funder

Swedish Cancer Society

Ministry of Science and Technology, Taiwan

Kaohsiung Medical University Hospital

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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