Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA, 15213, USA.
Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, 15213, USA.
Mol Nutr Food Res. 2022 Oct;66(19):e2200090. doi: 10.1002/mnfr.202200090. Epub 2022 Aug 31.
Human breast milk contains a variety of cell types that have potential roles in infant immunity and development. One challenge associates with defining the purpose(s) of milk cells in the infant is a poor understanding of the effect of digestion on cell fate.
This study first demonstrates that milk cell death occurs after gastric digestion in mice. Then flow cytometry and RT-PCR are used to understand the mechanism of human milk cell death and quantify live cell types before and after simulated gastric digestion. This study finds that digestion in simulated gastric fluid for 30 min reduces cell viability from 72% to 27%, with most cell death is caused by the acidic pH. The primary mechanism of cell death is caspase-mediated apoptosis. The non-cellular components of milk offer only mild protection against cell death from stomach acid.
Gastric digestion does not select for a specific resilient cell population to survive-most cell types die in equal proportions in the gastric environment. Taken together, these results provide a foundation with which to understand the fate of human breast milk cells in the infant's intestine and beyond.
人乳含有多种细胞类型,这些细胞在婴儿的免疫和发育中具有潜在作用。在确定乳汁细胞在婴儿中的作用(多个作用)时存在一个挑战,即人们对消化对细胞命运的影响了解甚少。
本研究首先证明了在小鼠中,胃消化后会发生乳细胞死亡。然后使用流式细胞术和 RT-PCR 来了解人乳细胞死亡的机制,并在模拟胃消化前后定量活细胞类型。本研究发现,在模拟胃液中消化 30 分钟会使细胞活力从 72%降低到 27%,大多数细胞死亡是由酸性 pH 值引起的。细胞死亡的主要机制是半胱氨酸天冬氨酸蛋白酶(caspase)介导的细胞凋亡。乳中的非细胞成分仅对胃酸引起的细胞死亡提供轻度保护。
胃消化不会选择特定的有弹性的细胞群来存活——大多数细胞类型在胃环境中以相等的比例死亡。综上所述,这些结果为理解人乳细胞在婴儿肠道及其他部位的命运提供了基础。