Osteoclast differentiation and function in aquaglyceroporin AQP9-null mice

被引:22
作者
Liu, Yangjian [1 ,2 ]
Song, Linhua [1 ]
Wang, Yiding [1 ]
Rojek, Aleksandra [3 ]
Nielsen, Soren [3 ]
Agre, Peter [1 ,4 ,5 ]
Carbrey, Jennifer M. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[3] Univ Aarhus, Water & Salt Res Ctr, DK-8000 Aarhus, Denmark
[4] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[5] Johns Hopkins Bloomberg Sch Publ Hlth, Malaria Res Inst, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
aquaglyceroporin; aquaporin; aquaporin 9 (AQP9); bone; osteoclast; MOLECULAR CHARACTERIZATION; BONE-RESORPTION; AQUAPORIN-9; GLYCEROL; CELLS; AQP9; CHANNELS; LIVER; EXPRESSION; PROTEIN;
D O I
10.1042/BC20080083
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Background information. Osteoclasts are cells specialized for bone resorption and play important roles in bone growth and calcium homoeostasis. Differentiation of osteoclasts involves fusion of bone marrow macrophage mononuclear precursors in response to extracellular signals. A dramatic increase in osteoclast cell volume occurs during osteoclast biogenesis and is believed to be mediated by AQP9 (aquaporin 9), a membrane protein that can rapidly transport water and other small neutral solutes across cell membranes. Results. In the present study we report an increase in expression of AQP9 during differentiation of a mouse macrophage cell line into osteoclasts. Bone marrow macrophages from wild-type and AQP9-null mice differentiate into osteoclasts that have similar morphology, contain comparable numbers of nuclei, and digest synthetic bone to the same extent. Bones from wild-type and AQP9-null mice contain similar numbers of osteoclasts and have comparable density and structure as measured by X-ray absorptiometry and microcomputed tomography. Conclusions. Our results confirm that AQP9 expression rises during osteoclast biogenesis, but indicate that AQP9 is not essential for osteoclast function or differentiation under normal physiological conditions.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 24 条
[1]
Pharmacological comparison of swelling-activated excitatory amino acid release and Cl- currents in cultured rat astrocytes [J].
Abdullaev, Iskandar F. ;
Rudkouskaya, Alena ;
Schools, Gary P. ;
Kimelberg, Harold K. ;
Mongin, Alexander A. .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 572 (03) :677-689
[2]
Aquaporin water channels - from atomic structure to clinical medicine [J].
Agre, P ;
King, LS ;
Yasui, M ;
Guggino, WB ;
Ottersen, OP ;
Fujiyoshi, Y ;
Engel, A ;
Nielsen, S .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 542 (01) :3-16
[3]
Involvement of aquaporin 9 in osteoclast differentiation [J].
Aharon, Refael ;
Bar-Shavit, Zvi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (28) :19305-19309
[4]
FHL2 inhibits the activated osteoclast in a TRAF6-dependent manner [J].
Bai, ST ;
Kitaura, H ;
Zhao, HB ;
Chen, J ;
Müller, JM ;
Schüle, R ;
Darnay, B ;
Novack, DV ;
Ross, FP ;
Teitelbaum, SL .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (10) :2742-2751
[5]
CELL-MEDIATED EXTRACELLULAR ACIDIFICATION AND BONE-RESORPTION - EVIDENCE FOR A LOW PH IN RESORBING LACUNAE AND LOCALIZATION OF A 100-KD LYSOSOMAL MEMBRANE-PROTEIN AT THE OSTEOCLAST RUFFLED BORDER [J].
BARON, R ;
NEFF, L ;
LOUVARD, D ;
COURTOY, PJ .
JOURNAL OF CELL BIOLOGY, 1985, 101 (06) :2210-2222
[6]
Aquaglyceroporin AQP9: Solute permeation and metabolic control of expression in liver [J].
Carbrey, JM ;
Gorelick-Feldman, DA ;
Kozono, D ;
Praetorius, J ;
Nielsen, S ;
Agre, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (05) :2945-2950
[7]
Cathepsin K, but not cathepsins B, L, or S, is abundantly expressed in human osteoclasts [J].
Drake, FH ;
Dodds, RA ;
James, IE ;
Connor, JR ;
Debouck, C ;
Richardson, S ;
LeeRykaczewski, E ;
Coleman, L ;
Rieman, D ;
Barthlow, R ;
Hastings, G ;
Gowen, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12511-12516
[8]
Immunolocalization of AQP9 in liver, epididymis, testis, spleen, and brain [J].
Elkjær, ML ;
Vajda, Z ;
Nejsum, LN ;
Kwon, TH ;
Jensen, UB ;
Amiry-Moghaddam, M ;
Frokiær, J ;
Nielsen, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 276 (03) :1118-1128
[9]
Phloretin differentially inhibits volume-sensitive and cyclic AMP-activated, but not Ca-activated, Cl- channels [J].
Fan, HT ;
Morishima, S ;
Kida, H ;
Okada, Y .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 133 (07) :1096-1106
[10]
U0126 and PD98059, specific inhibitors of MEK, accelerate differentiation of RAW264.7 cells into osteoclast-like cells [J].
Hotokezaka, H ;
Sakai, E ;
Kanaoka, K ;
Saito, K ;
Matsuo, K ;
Kitaura, H ;
Yoshida, N ;
Nakayama, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :47366-47372