Maternal immune activation does not affect maternal microchimeric cells

被引:0
作者
Borges, Alexandria [1 ]
Irie, Naoki [2 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, 7-3-1 Bunkyo Ku, Hongo, Tokyo 1130033, Japan
[2] SOKENDAI, Res Ctr Integrat Evolutionary Sci, Hayama, Kanagawa 2400193, Japan
来源
BIOLOGY OPEN | 2024年 / 13卷 / 12期
关键词
Maternal microchimerism; Immunology; Embryonic development; Cell-level epigenetics; HLA; QUANTIFICATION; PATHOGENESIS; TRAFFICKING; LYMPHOCYTES; MOTHER; FETUS;
D O I
10.1242/bio.061830
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We are naturally chimeras. Apart from our own cells originating from the fertilized egg, placental mammals receive small numbers of maternal cells called maternal microchimerism (MMc) that persist throughout one's whole life. Not only are varying frequencies of MMc cells reported in seemingly contradicting phenomena, including immune tolerance and possible contribution to autoimmune-like disease, but frequencies are observable even among healthy littermates showing varying MMc frequencies and cell type repertoire. These varying differences in MMc frequencies or cell types could be contributing to the diverse phenomena related to MMc. However, factors biasing these MMc differences remain largely unknown. Here, we tested whether immunological activation leads to differing MMc frequencies, based on our recent study that suggests that most maternal cells are immune-related. Unexpectedly, fluorescence-activated cell sorting analysis on the murine spleen, thymus, and liver following maternal immune activation by mid- gestational lipopolysaccharide intraperitoneal injections detected no significant difference in the number, or ratio of, immune-related maternal cells in the tested embryonic organs of healthy offspring. These findings suggest that MMc frequencies remain stable even under immune-activated conditions, implying a possible control system of MMc migration against changes in the immunological conditions.
引用
收藏
页数:8
相关论文
共 38 条
  • [1] Aydin M. S., Yig it E. N., Vatandaslar E., Erdog an E., Ozturk G., Transfer and integration of breast milk stem cells to the brain of suckling pups, Sci. Rep, 8, (2018)
  • [2] Bakkour S., Baker C. A. R., Tarantal A. F., Wen L., Busch M. P., Lee T. H., Mccune J. M., Analysis of maternal microchimerism in rhesus monkeys (Macaca mulatta) using real-time quantitative PCR amplification of MHC polymorphisms, Chimerism, 5, pp. 6-15, (2014)
  • [3] Balle C., Armistead B., Kiravu A., Song X., Happel A.-U., Hoffmann A. A., Kanaan S. B., Nelson J. L., Gray C. M., Jaspan H. B., Et al., Factors influencing maternal microchimerism throughout infancy and its impact on infant T cell immunity, J. Clin. Investig, 132, (2022)
  • [4] Borges A., Castellan F., Irie N., Emergent roles of maternal microchimerism in postnatal development, Dev. Growth Diff, 65, pp. 75-81, (2023)
  • [5] Castellan F. S., Irie N., Postnatal depletion of maternal cells biases T lymphocytes and natural killer cells’ profiles toward early activation in the spleen, Biol. Open, 11, (2022)
  • [6] Dutta P., Burlingham W. J., Microchimerism: tolerance vs. sensitization, Curr. Opin. Organ Transplantat, 16, pp. 359-365, (2011)
  • [7] Dutta P., Molitor-Dart M., Bobadilla J. L., Roenneburg D. A., Yan Z., Torrealba J. R., Burlingham W. J., Microchimerism is strongly correlated with tolerance to noninherited maternal antigens in mice, Blood, 114, pp. 3578-3587, (2009)
  • [8] Fricke E. M., Elgin T. G., Gong H., Reese J., Gibson-Corley K. N., Weiss R. M., Zimmerman K., Bowdler N. C., Kalantera K. M., Mills D. A., Et al., Lipopolysaccharide-induced maternal inflammation induces direct placental injury without alteration in placental blood flow and induces a secondary fetal intestinal injury that persists into adulthood, Am. J. Reprod. Immunol, 79, (2018)
  • [9] Fujimoto K., Nakajima A., Hori S., Irie N., Whole embryonic detection of maternal microchimeric cells highlights significant differences in their numbers among individuals, PLoS ONE, 16, (2021)
  • [10] Fujimoto K., Nakajima A., Hori S., Tanaka Y., Shirasaki Y., Uemura S., Irie N., Whole-embryonic identification of maternal microchimeric cell types in mouse using single-cell RNA sequencing, Sci. Rep, 12, (2022)