Dergiler / Turkish Journal of Biology / 2017 / Cilt: 41 - Sayı: 1

The Sca1+ mesenchymal stromal subpopulation promotes dendritic cell commitment in the niche

Sayfa
58–65
Yayın Tarihi
2022-10-17
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Meanwhile, Sca1+ MSCs also mediate the activation and migration capabilities of DCs.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:The hematopoietic microenvironment regulates self-renewal and differentiation of hematopoietic stem cells.
📊
Temel Bulgular & Veri:The current study showed that one of the bone-related Sca1+ MSCs enhanced bone marrow cell differentiation into DCs by direct cell-to-cell contact.
💡
Sonuç & Katkı:Meanwhile, Sca1+ MSCs also mediate the activation and migration capabilities of DCs.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

The hematopoietic microenvironment regulates self-renewal and differentiation of hematopoietic stem cells. Mesenchymal stromal cells (MSCs) contribute to the niche and participate in supporting dendritic cell (DC) commitment in vitro and in vivo. However, due to MSCs being heterogenic, it is necessary to understand the function of the MSC subpopulation in modulating the DC commitment. The current study showed that one of the bone-related Sca1+ MSCs enhanced bone marrow cell differentiation into DCs by direct cell-to-cell contact. Furthermore, the expression of STAT3 and STAT5 genes decreased in supernatant cells after Sca1+ MSCs were cocultured with bone marrow cells. In contrast, the expression level of caspase-3 in cells increased. At the same time, the presentation of costimulatory molecules CD80/CD86 and the migration of activated DCs towards lymph nodes were augmented by Sca1+ MSCs. The results demonstrated that the Sca1+ MSC subpopulation promotes the differentiation of bone marrow cells into DCs by direct cell-to-cell contact via STAT3/STAT5 and caspase-3 signaling. Meanwhile, Sca1+ MSCs also mediate the activation and migration capabilities of DCs.

🔖

Bu Makaleye Atıf Yap

LI, N., HU, X., XU, J., LIU, Z., CHEN, Y., YIN, D., WANG, Y., AN, N., WEN, F., XIN, J., ZHANG, H., YIN, W. (2022). The Sca1+ mesenchymal stromal subpopulation promotes dendritic cell commitment in the niche. Turkish Journal of Biology, Cilt: 41 - Sayı: 1, 58–65. https://ajindex.com/articles/600300

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (14)

  1. Abdul-Ghani M, Megeney LA (2008). Rehabilitation of a contract killer: caspase-3 directs stem cell differentiation. Cell Stem Cell 2: 515-516.
  2. Belz GT, Nutt SL (2012). Transcriptional programming of the dendritic cell network. Nat Rev Immunol 12: 101-113.
  3. Chen Y, Chen Y, Yin D, Wang Y, Liu Z, An N, Wen F, Li N, Xin J, Hu X et al. (2016a). The Sca-1+ mesenchymal stromal cells modulate macrophage commitment and function. Turk J Biol 40: 473-483.
  4. Chen Y, Yang J, Zhang HJ, Fan H, An N, Xin J, Li N, Xu J, Yin W, Wu Z et al. (2016b). Sca-1+ mesenchymal stromal cells inhibit splenic marginal zone B lymphocytes commitment through Caspase-3. Cell Biol Int 40: 549-559.
  5. Chiesa S, Morbelli S, Morando S, Massollo M, Marini C, Bertoni A, Frassoni F, Bartolome ST, Sambuceti G, Traggiai E et al. (2011). Mesenchymal stem cells impair in vivo T-cell priming by dendritic cells. P Natl Acad Sci USA 108: 17384-17389.
  6. Ding L, Morrison SJ (2013). Haematopoietic stem cells and early lymphoid progenitors occupy distinct bone marrow niches. Nature 495: 231-235.
  7. Ding L, Saunders TL, Enikolopov G, Morrison SJ (2012). Endothelial and perivascular cells maintain haematopoietic stem cells. Nature 481: 457-462.
  8. Esashi E, Wang YH, Perng O, Qin XF, Liu YJ, Watowich SS (2008). The signal transducer STAT5 inhibits plasmacytoid dendritic cell development by suppressing transcription factor IRF8. Immunity 28: 509-520.
  9. Frenette PS, Pinho S, Lucas D, Scheiermann C (2013). Mesenchymal stem cell: keystone of the hematopoietic stem cell niche and a stepping-stone for regenerative medicine. Annu Rev Immunol 31: 285-316.
  10. Galderisi U, Giordano A (2014). The gap between the physiological and therapeutic roles of mesenchymal stem cells. Med Res Rev 34: 1100-1126.
  11. Ganguly D, Haak S, Sisirak V, Reizis B (2013). The role of dendritic cells in autoimmunity. Nat Rev Immunol 13: 566-577.
  12. Hammer GE, Ma A (2013). Molecular control of steady-state dendritic cell maturation and immune homeostasis. Annu Rev Immunol 31: 743-791.
  13. Hudson JE, Mills RJ, Frith JE, Brooke G, Jaramillo-Ferrada P, Wolvetang EJ, Cooper-White JJ (2011). A defined medium and substrate for expansion of human mesenchymal stromal cell progenitors that enriches for osteo- and chondrogenic precursors. Stem Cells Dev 20: 77-87.
  14. Jiang XX, Zhang Y, Liu B, Zhang SX, Wu Y, Yu XD, Mao N (2005). Human mesenchymal stem cells inhibit differentiation and function of monocyte-derived dendritic cells. Blood 105: 4120- 4126. Lai HY, Yang MJ, Wen KC, Chao KC, S