Adult lung side population cells have mesenchymal stem cell potential

被引:84
作者
Martin, J. [1 ,3 ]
Helm, K. [3 ]
Ruegg, P. [5 ]
Varella-Garcia, M. [2 ,3 ]
Burnham, E. [4 ]
Majka, S. [1 ,3 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Div Cardiol, Cardiol Pulm Lab, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Div Med Oncol, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Ctr Canc, Denver, CO 80262 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Med, Dept Med Pulm & Crit Care Med, Denver, CO 80262 USA
[5] IHC Technol, Aurora, CO USA
关键词
adult stem cells; cell therapy; lung side population cells; mesenchymal stem cells;
D O I
10.1080/14653240801895296
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background The development of stem cell therapy for pulmonary diseases remains a challenge. Many diverse cell types reside within the lung and a common stem cell has not yet been identified. A basic understanding of lung stem cell fate during disease may prove important for drug intervention as well as autologous therapies. Niches for resident mesenchymal stem cells (MSC) have been identified in many adult tissues and more recently in the lung. We present data to confirm the observation that non-hematopoietic CD45(neg) lung side population (SP) cells contain MSC, single cells capable of multilineage differentiation. Methods We carried these observations forward by analyzing the MSC potential of single-cell clones, as well as their chromosomal stability and telomerase activity. Results The expression of MSC markers was characterized in mouse CD45(neg) lung SP by flow cytometry on freshly isolated or cultured clonal populations. The karyotype of these cells was subsequently assayed by banding analysis, and telomerase activity was assessed using quantitative polymerase chain reaction. MSC differentiation potential was confirmed by the characteristic ability of single-cell clones to differentiate into cells of three mesenchymal lineages, chondrocytes, adipocytes and osteocytes. Differentiation was confirmed by histochemical analysis. All analyzed populations of CD45(neg) lung SP expressed mesenchymal markers (CD44, CD90, CD105, CD106, CD73 and Sca-I) and lacked hematopoietic markers (CD45, c-kit, CD11b, CD34 and CD14). The cultured and clonal CD45(neg) lung SP had normal chromosomal structures and expressed high levels of telomerase. After being expanded and cultured in differentiation medium, all populations of CD45(neg) lung SP demonstrated adipogenic, osteogenic and chrondrogenic potential. Adult CD45(neg) lung SP cells are a source of MSC. Discussion In defining this tissue-specific stem cell population in the lung, we are now better able to clarify a potential role for them in lung diseases.
引用
收藏
页码:140 / 151
页数:12
相关论文
共 45 条
  • [1] Alteration of marrow cell gene expression, protein production, and engraftment into lung by lung-derived microvesicles: A novel mechanism for phenotype modulation
    Aliotta, Jason M.
    Sanchez-Guijo, Fermin M.
    Dooner, Gerri J.
    Johnson, Kevin W.
    Dooner, Mark S.
    Greer, Kenneth A.
    Greer, Deborah
    Pimentel, Jeffrey
    Kolankiewicz, Lutz M.
    Puente, Napoleon
    Faradyan, Sam
    Ferland, Paulette
    Bearer, Elaine L.
    Passero, Michael A.
    Adedi, Mehrdad
    Colvin, Geralt A.
    Quesenberry, Peter J.
    [J]. STEM CELLS, 2007, 25 (09) : 2245 - 2256
  • [2] Side population cells from diverse adult tissues are capable of in vitro hematopoietic differentiation
    Asakura, A
    Rudnicki, MA
    [J]. EXPERIMENTAL HEMATOLOGY, 2002, 30 (11) : 1339 - 1345
  • [3] Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo
    Bartholomew, A
    Sturgeon, C
    Siatskas, M
    Ferrer, K
    McIntosh, K
    Patil, S
    Hardy, W
    Devine, S
    Ucker, D
    Deans, R
    Moseley, A
    Hoffman, R
    [J]. EXPERIMENTAL HEMATOLOGY, 2002, 30 (01) : 42 - 48
  • [4] Mesenchymal stromal cell-like characteristics of corneal keratocytes
    Choong, P-F
    Mok, P-L
    Cheong, S-K
    Then, K-Y
    [J]. CYTOTHERAPY, 2007, 9 (03) : 252 - 258
  • [5] Stem cells and cancer: Two faces of eve
    Clarke, MF
    Fuller, M
    [J]. CELL, 2006, 124 (06) : 1111 - 1115
  • [6] Isolation of a mesenchymal cell population from murine dermis that contains progenitors of multiple cell lineages
    Crigler, Lauren
    Kazhanie, Amita
    Yoon, Tae-Jin
    Zakhari, Julia
    Anders, Joanna
    Taylor, Barbara
    Virador, Victoria M.
    [J]. FASEB JOURNAL, 2007, 21 (09) : 2050 - 2063
  • [7] Mesenchymal-epithelial interactions in lung development and repair: are modeling and remodeling the same process?
    Demayo, F
    Minoo, P
    Plopper, CG
    Schuger, L
    Shannon, J
    Torday, JS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 283 (03) : L510 - L517
  • [8] Stem cell niches in the mouse airway
    Engelhardt, JF
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 24 (06) : 649 - 652
  • [9] Elevated telomerase activity and minimal telomere loss in cord blood long-term cultures with extensive stem cell replication
    Gammaitoni, L
    Weisel, KC
    Gunetti, M
    Wu, KD
    Bruno, S
    Pinelli, S
    Bonati, A
    Aglietta, M
    Moore, MAS
    Piacibello, W
    [J]. BLOOD, 2004, 103 (12) : 4440 - 4448
  • [10] Gebb SA, 2000, DEV DYNAM, V217, P159, DOI 10.1002/(SICI)1097-0177(200002)217:2<159::AID-DVDY3>3.3.CO