An article published this year in “JOURNAL OF CELLULAR PHYSIOLOGY” using
our anti Human
CD105 (Clon 2H6F11), by our customers from Dipartimento Scienze Cliniche e
Molecolari, Clinica di Ematologia, Università Politecnica delle Marche, Ancona,
Italy, in the analysis of how Bone marrow adipocytes support haematopoietic
stem cell survival. Congrats and Thanks.
Summary:
In bone marrow (BM), haematopoietic
elements are mingled with adipocytes (BM-A), which are the most abundant
stromal component in the niche. BM-A progressively increase with ageing,
eventually occupying up to 50% of BM cavities.

Findings demonstrated that BM-A are
capable of supporting HSC survival in the LTC-IC assay, since after 5 weeks of
co-culture, HSC were still able to proliferate and differentiate. Furthermore,
critical molecules such as C-X-C motif chemokine 12 (CXCL12), interleukin
(IL)-8, colony-stimulating factor 3 (CSF3), and leukaemia inhibitory factor
(LIF), were expressed at similar levels in BM-A and in primary human BM
mesenchymal stromal cells (BM-MSC), whereas IL-3 was higher in BM-A.
Interestingly, BM-A displayed a
different gene expression profile compared with subcutaneous adipose tissue
adipocytes (AT-A) collected from abdominal surgery patients, especially in
terms of regulation of lipid metabolism, stemness genes and white-to-brown
differentiation pathways. Accordingly, analysis of the gene pathways involved
in haematopoiesis regulation showed that BM-A are more closely related to
BM-MSC than to AT-A.
The present data suggest that BM-A
play a supporting role in the haematopoietic niche and directly sustain HSC
survival.
Reference:
Product link:
Anti Human CD105 (clon 2H6F1): http://www.immunostep.com/antibodies/2792-cd105.html
No comments:
Post a Comment