CD56 Expression Marks Human Group 2 Innate Lymphoid Cell Divergence from a Shared NK Cell and Group 3 Innate Lymphoid Cell Developmental Pathway.
CD56 Expression Marks Human Group 2 Innate Lymphoid Cell Divergence from a Shared NK Cell and Group 3 Innate Lymphoid Cell Developmental Pathway.
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DOI:
10.1016/j.immuni.2018.08.010
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发表时间:
2018-09-18
期刊:
影响因子:
32.4
通讯作者:
Freud AG
中科院分区:
文献类型:
--
作者:
Chen L;Youssef Y;Robinson C;Ernst GF;Carson MY;Young KA;Scoville SD;Zhang X;Harris R;Sekhri P;Mansour AG;Chan WK;Nalin AP;Mao HC;Hughes T;Mace EM;Pan Y;Rustagi N;Chatterjee SS;Gunaratne PH;Behbehani GK;Mundy-Bosse BL;Caligiuri MA;Freud AG
According to the established model of murine innate lymphoid cell (ILC) development, helper ILCs develop separately from natural killer (NK) cells. However, it is unclear how helper ILCs and NK cells develop in humans. Here we elucidated key steps of NK cell, ILC2, and ILC3 development within human tonsils using ex vivo molecular and functional profiling and lineage differentiation assays. We demonstrated that while tonsillar NK cells, ILC2s, and ILC3s originated from a common CD34−CD117+ ILC precursor pool, final steps of ILC2 development deviated independently and became mutually exclusive from those of NK cells and ILC3s, whose developmental pathways overlapped. Moreover, we identified a CD34−CD117+ ILC precursor population that expressed CD56 and gave rise to NK cells and ILC3s but not to ILC2s. These data support a model of human ILC development distinct from the mouse, whereby human NK cells and ILC3s share a common developmental pathway separate from ILC2s. Human innate lymphoid cells (ILCs) develop from tissue-resident ILC precursors (ILCPs) in secondary lymphoid tissues. Here, Chen and colleagues describe a model of human ILC development in tonsils in which NK cells and group 3 ILCs derive from a CD56+ subset of ILCPs that cannot differentiate into group 2 ILCs.
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影响因子:
64.8
作者:
Cella, Marina;Fuchs, Anja;Vermi, William;Facchetti, Fabio;Otero, Karel;Lennerz, Jochen K. M.;Doherty, Jason M.;Mills, Jason C.;Colonna, Marco
通讯作者:
Colonna, Marco
影响因子:
17.1
作者:
Horowitz A;Strauss-Albee DM;Leipold M;Kubo J;Nemat-Gorgani N;Dogan OC;Dekker CL;Mackey S;Maecker H;Swan GE;Davis MM;Norman PJ;Guethlein LA;Desai M;Parham P;Blish CA
通讯作者:
Blish CA
影响因子:
32.4
作者:
Bernink, Jochem H.;Krabbendam, Lisette;Spits, Hergen
通讯作者:
Spits, Hergen
DOI:
10.1126/science.1198704
发表时间:
2011-05-06
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Bendall SC;Simonds EF;Qiu P;Amir el-AD;Krutzik PO;Finck R;Bruggner RV;Melamed R;Trejo A;Ornatsky OI;Balderas RS;Plevritis SK;Sachs K;Pe'er D;Tanner SD;Nolan GP
通讯作者:
Nolan GP
影响因子:
30.5
作者:
Bernink, Jochem H.;Peters, Charlotte P.;Spits, Hergen
通讯作者:
Spits, Hergen