Table 1.
Overview of representative human organoids.
| Organ types | Available cell types | Characteristics/function | Limitations |
|---|---|---|---|
| Brain | Neural stem/progenitor cells, radial glia, neurons, astrocytes, and oligodendrocytes[71,135,136] | Modeling development of specific brain regions, cortical layering, early neurogenesis, synapse formation, and spontaneous electrical activity | Size limit due to oxygen and nutrient diffusion constraints; lack of microvascular differentiation; absence of microglial cells; can not replicate complex neural connections and projection; lack of higher-order neural network functions |
| Spinal cord | Motor neurons, interneurons, progenitor cells, astrocytes, and oligodendrocytes[137–139] | Modeling the early development of the neural tube, axon growth, neurotransmission of sensory inputs and motor outputs | Limited maturation of spinal structures; incomplete myelination; lack of peripheral tissue integration; absence of immune response |
| Retina | Photoreceptors, bipolar, horizontal, amacrine, ganglion cells, and Müller cells[140–142] | Modeling simulating light signal processing | Lack of vascularization; limited optic nerve formation and incomplete retinal structure; lack a specific cone cell-rich region similar to the human central fovea |
| Heart | Cardiomyocytes, cardiac fibroblasts, endothelial cells, epicardial cells, and endocardial cells[143–145] | Modeling functional characteristics such as contractility, cavity formation, action potential propagation, and forming vascular-like structures | Incomplete heart chamber formation; limited electrical activity; insufficient integration with vasculature and lack of true perfusion through blood vessels |
| Liver | Hepatocytes, cholangiocytes, Kupffer cells, hepatic stellate cells, and liver sinusoidal endothelial cells[146–148] | Modeling the production of albumin and the secretion of bile acids and accumulating glycogen and producing albumin and bile acids | Limited bile duct formation and immune interactions; lack of full functional vascular network; lack of full metabolic complexity |
| Kidney | Multiple lineages such as nephron progenitors, ureteric buds, stromal progenitors, and vascular endothelial cells[21,73,149] | Modeling key renal functions such as glomerular filtration and tubular reabsorption | Lack of full functional vascular network and filtration systems; lack of distal nephrons (distal renal tubules and loops of Henle); insufficient maturation of the collecting ducts; limited nephron complexity |
| Lung | Basal cells, club cells, alveolar type 2 epithelial cells[150–152] | Replicating the functional capabilities of basal cells in self-renewal and differentiation, club cells in mucin production for airway protection, and alveolar type 2 epithelial cells in differentiating into AEC1s for gas exchange | Lack of terminal cellular maturity, particularly mature alveolar lineages, and progressive branching formation; absence of vascularization and immune cells |
| Pancreas | Islet cells, ductal cells, and acinar cells, which can differentiate into various pancreatic cell types, including β-cells, under specific culture conditions[153–155] | Replicating insulin secretion and endocrine function | Lack of islet maturation; low differentiation efficiency and long-term instability; lack of a complete vascular system and interactions with other pancreatic cell types and non-pancreatic tissues |
| Intestine | Intestinal stem cells, epithelial cells, including absorptive enterocytes and secretory cells like goblet, Paneth, and enteroendocrine cells[156–158] | Modeling the natural polarity and functionality of the intestinal epithelium | Lack of the full complement of the in vivo intestinal environment, including a complete immune cell community, neural cells, and microbiota |
| Blood vessels | Endothelial cells, pericytes, and vascular smooth muscle cells[159–161] | Modeling angiogenesis, vascular maturation, and the interaction between endothelial cells and pericytes; blood vessels can be formed within 2–3 weeks | Limited vessel maturation and connection structures; lack of perfusable capillary networks; insufficient integration with other tissues or organoids for perfusion |
AEC1s: alveolar epithelial type 1 cells.