Allegra Alessandro, Coppolino Giuseppe, Bolignano Davide, Giacobbe Maria Stella, Alonci Andrea, D'Angelo Arianna, Bellomo Giacomo, Teti Diana, Loddo Saverio, Musolino Caterina, Buemi Michele
Division of Hematology, University of Messina, Messina, Italy.
J Nephrol. 2009 Jul-Aug;22(4):463-75.
Bone marrow-derived, CD34+ progenitor cells have been shown to promote the repair of damaged tissues, offering promise for the treatment of hereditary and acquired human diseases. These cells in fact differentiate into endothelia, hematopoietic cells and possibly neurons, fibroblasts and muscle. CD34+ and AC133+ progenitor cells may participate in neovascularization by differentiating into endothelial cells. Circulating bone marrow-derived endothelial cells home to sites of neovascularization and stimulate healing of injured tissues but also promote restenosis, tumor growth and inflammatory disease. These cells may thus participate in tissue regeneration or pathogenesis of several diseases. Although the molecular mechanisms that promote the homing and recruitment of bone marrow-derived progenitor cells to remodeling tissues remain unclear the evidence that these cells promote tissue repair is strong.
骨髓来源的CD34+祖细胞已被证明可促进受损组织的修复,为治疗遗传性和后天性人类疾病带来了希望。这些细胞实际上可分化为内皮细胞、造血细胞,还可能分化为神经元、成纤维细胞和肌肉。CD34+和AC133+祖细胞可能通过分化为内皮细胞参与新血管形成。循环中的骨髓来源内皮细胞归巢至新血管形成部位,刺激受伤组织愈合,但也会促进再狭窄、肿瘤生长和炎症性疾病。因此,这些细胞可能参与多种疾病的组织再生或发病机制。尽管促进骨髓来源祖细胞归巢和募集至重塑组织的分子机制尚不清楚,但这些细胞促进组织修复的证据确凿。