Parathyroid Hormone Enhances Hematopoietic Expansion Via Upregulation of Cadherin-11 in Bone Marrow Mesenchymal Stromal Cells

Author:

Yao Hisayuki1,Miura Yasuo1,Yoshioka Satoshi12,Miura Masako3,Hayashi Yoshihiro14,Tamura Akihiro1,Iwasa Masaki14,Sato Atsushi1,Hishita Terutoshi5,Higashi Yayoi6,Kaneko Hitomi7,Ashihara Eishi8,Ichinohe Tatsuo9,Hirai Hideyo1,Maekawa Taira1

Affiliation:

1. Department of Transfusion Medicine and Cell Therapy Kyoto University Hospital, Kyoto, Japan

2. Department of Hematology/Oncology Kyoto University Graduate School of Medicine, Kyoto, Japan

3. Department of Medicine and Clinical Science Kyoto University Graduate School of Medicine, Kyoto, Japan

4. Division of Gastroenterology and Hematology Shiga University of Medical Science, Ōtsu, Shiga, Japan

5. Department of Hematology National Hospital Organization Himeji Medical Center, Himeji, Hyogo, Japan

6. Department of Gynecology and Obstetrics Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan

7. Department of Hematology Osaka Red Cross Hospital, Osaka, Japan

8. Department of Clinical and Translational Physiology Kyoto Pharmaceutical University, Kyoto, Japan

9. Department of Hematology and Oncology Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan

Abstract

Abstract Parathyroid hormone (PTH) stimulates hematopoiesis in mouse models. The involvement of osteoblasts in this process has been well investigated; however, the effects of PTH on human hematopoiesis and bone marrow mesenchymal stromal cells (BM-MSCs) are unclear. Here, we show that BM-MSCs contribute to the hematopoiesis-stimulating effects of PTH via upregulation of cadherin-11 (CDH11). When culture-expanded human BM-MSCs were stimulated with PTH, their ability to expand cocultured CD34+ hematopoietic progenitor cells (HPCs) was enhanced. Furthermore, when PTH-treated BM-MSCs were subcutaneously implanted into NOD/SCID mice, the induction of hematopoietic cells was enhanced. Culture-expanded human BM-MSCs expressed CDH11, and the level of CDH11 expression increased following PTH stimulation. Depletion of CDH11 expression in BM-MSCs using small interfering RNA abolished the enhancement of HPC expansion by PTH-treated BM-MSCs. In lethally irradiated mice that underwent BM transplantation, CDH11 expression in BM-MSCs was higher and survival was better in PTH-treated mice than in control mice. The number of hematopoietic cells in BM and the number of red blood cells in peripheral blood were higher in PTH-treated mice than in control mice. Our results demonstrate that PTH stimulates hematopoiesis through promoting the upregulation of CDH11 expression in BM-MSCs, at least in part. PTH treatment may be an effective strategy to enhance the ability of BM-MSCs to support hematopoiesis. Stem Cells  2014;32:2245–2255

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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