TY - JOUR
T1 - Osteoclasts promote the formation of hematopoietic stem cell niches in the bone marrow
AU - Mansour, Anna
AU - Abou-Ezzi, Grazia
AU - Sitnicka, Ewa
AU - Jacobsen, Sten Eirik W.
AU - Wakkach, Abdelilah
AU - Blin-Wakkach, Claudine
PY - 2012/3/12
Y1 - 2012/3/12
N2 - Formation of the hematopoietic stem cell (HSC) niche in bone marrow (BM) is tightly associated with endochondral ossification, but little is known about the mechanisms involved. We used the oc/oc mouse, a mouse model with impaired endochondral ossification caused by a loss of osteoclast (OCL) activity, to investigate the role of osteoblasts (OBLs) and OCLs in the HSC niche formation. The absence of OCL activity resulted in a defective HSC niche associated with an increased proportion of mesenchymal progenitors but reduced osteoblastic differentiation, leading to impaired HSC homing to the BM. Restoration of OCL activity reversed the defect in HSC niche formation. Our data demonstrate that OBLs are required for establishing HSC niches and that osteoblastic development is induced by OCLs. These findings broaden our knowledge of the HSC niche formation, which is critical for understanding normal and pathological hematopoiesis.
AB - Formation of the hematopoietic stem cell (HSC) niche in bone marrow (BM) is tightly associated with endochondral ossification, but little is known about the mechanisms involved. We used the oc/oc mouse, a mouse model with impaired endochondral ossification caused by a loss of osteoclast (OCL) activity, to investigate the role of osteoblasts (OBLs) and OCLs in the HSC niche formation. The absence of OCL activity resulted in a defective HSC niche associated with an increased proportion of mesenchymal progenitors but reduced osteoblastic differentiation, leading to impaired HSC homing to the BM. Restoration of OCL activity reversed the defect in HSC niche formation. Our data demonstrate that OBLs are required for establishing HSC niches and that osteoblastic development is induced by OCLs. These findings broaden our knowledge of the HSC niche formation, which is critical for understanding normal and pathological hematopoiesis.
UR - http://www.scopus.com/inward/record.url?scp=84860378826&partnerID=8YFLogxK
U2 - 10.1084/jem.20110994
DO - 10.1084/jem.20110994
M3 - Article
C2 - 22351931
AN - SCOPUS:84860378826
SN - 0022-1007
VL - 209
SP - 537
EP - 549
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 3
ER -