
The distinction between human and mouse NK cells lies in the occurrence of NK cells in the lymph nodes. Typically, human NK cells reside naturally within the lymph nodes. Conversely, in untreated or unmanipulated mice, NK cells are absent from the lymph nodes, and their presence is only observed after external stimulation.
NKp46, a unique stimulatory receptor, is exclusively expressed in all human NK cells and plays a pivotal role in mediating natural cytotoxicity.
Athymic nude mice are frequently utilized for xenograft transplants, attributed to their lack of a thymus. These mice are capable of hosting xenografts derived from cell lines of different species without rejecting the foreign xenograft. Consequently, this allows researchers to delve into the intricate nature of metastasized cancer in its advanced forms.
Human NK cells are capable of expressing the pan-ILC markers, CD127 and CD161, as reported in studies (18-20). However, NK cells are primarily distinguished by their unique surface expression profile, which includes CD16 (FcγRIIIA), CD94/NKG2 heterodimers, killer immunoglobulin-like receptors (KIRs), NKG2D, and NKp80 (21). This characteristic expression pattern allows for the identification and distinction of NK cells from other immune cell types.
The surface distribution of CD27 and CD11b markers allows for the categorization of mouse natural killer (NK) cells into four distinct subpopulations: CD11blowCD27low, CD11blowCD27high, CD11bhighCD27high, and CD11bhighCD27low. In order to elucidate the developmental interplay among these four subpopulations, we employed a multifaceted approach.scc7 cell line
CD64, also known as FcγRI, stands out as the sole FcR with a profound affinity for IgG. Similar to CD16A, it recognizes and interacts with the same IgG isotypes. However, a crucial distinction lies in the fact that it is absent in human NK cells. With the aim of bolstering their ADCC capabilities, we have successfully engineered human NK cells to express recombinant CD64. 24th February, 2022
CD11b, also known as Mac-1, serves as an indicator for the activation and memory of CD8+ cytotoxic T cells during viral infections.
The proteins RAG1 and RAG2 initiate the process of V(D)J recombination by creating double-stranded breaks at the junction between a recombination signal sequence (RSS) and a coding segment.bend.3 cells
Dendritic Cells
Fully mature mouse DCs exhibit the integrin CD11c and can be categorized into three primary groups: lymphoid tissue-resident DCs (LT-DCs), migratory DCs (mDCs), and inflammatory DCs (infDCs) [78]. Among the LT-DC category, one finds the classic DCs (cDCs) as well as plasmacytoid-like DCs (pDCs).
In murine systems, the distinction of NK cells into various maturational stages is achieved through the differential expression of CD27 and CD11b markers. Younger NK cells, characterized by the presence of CD27 but absence of CD11b (CD27+CD11b−), traverse a transitional phase marked by the concurrent expression of both markers (CD27+CD11b+) before ultimately attaining a fully mature phenotype defined by the absence of CD27 and presence of CD11b (CD27−CD11b+) (Hayakawa andmyth S, 2006). This process of maturation offers insights into the developmental trajectory of NK cells in mice.mouse nk cell line
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