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Mesohyl
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The mesohyl, formerly known as mesenchyme or as mesoglea, is the gelatinous matrix within a sponge. It fills the space between the external pinacoderm and the internal choanoderm. The mesohyl resembles a type of connective tissue and contains several amoeboid cells such as amebocytes, as well as fibrils and skeletal elements. For a long time, it has been largely accepted that sponges lack true tissue, but it is currently debated as to whether mesohyl and pinacoderm layers are tissues.
The mesohyl is composed of the following main elements: collagen, fibronectin-like molecules, galectin, and a minor component, dermatopontin. These polypeptides form the extracellular matrix which provides the platform for specific cell adhesion as well as for signal transduction and cellular growth.
The mesohyl includes a noncellular colloidal mesoglea with embedded collagen fibers, spicules and various cells, being as such a type of mesenchyme.[1]
References
[edit]- ^ Brusca, R.C. & Brusca, G.J. (2003). Invertebrates. 2nd ed. Sunderland, Massachusetts: Sinauer Associates, p. 183.
Bibliography
[edit]- Lytle, Charles F.; Meyer, John R. (May 21, 2004). General Zoology Laboratory Guide (Fourteenth ed.). New York: McGraw-Hill. ISBN 978-0-07-234900-9.
- Müller, Werner E.G. (February 2003). "The Origin of Metazoan Complexity: Porifera as Integrated Animals". Integrative and Comparative Biology. 43 (1): 3–10. CiteSeerX 10.1.1.333.3174. doi:10.1093/icb/43.1.3. JSTOR 3884834. PMID 21680404.
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Mesohyl
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Overview
Definition
The mesohyl is the internal gelatinous matrix that fills the space between the outer pinacoderm, an epithelial-like layer of cells, and the inner choanoderm, consisting of flagellated collar cells, in sponges of the phylum Porifera.[5][6] This matrix serves as the primary non-cellular component of the sponge body, embedding various suspended elements that contribute to its overall architecture.[7] In sponges, the mesohyl functions as a mesenchyme-like connective tissue analogue, providing structural integrity and support without the presence of true organs or differentiated tissues typical of more complex animals.[6] It maintains the flexible yet robust form of the sponge, allowing it to withstand physical stresses in aquatic environments while facilitating basic physiological processes.[7] The mesohyl constitutes the bulk of the sponge body across the three primary architectural plans: asconoid, syconoid, and leuconoid.[8] In asconoid sponges, it forms the thin walls surrounding the central spongocoel; in syconoid forms, it separates incurrent canals from choanocyte chambers; and in the more complex leuconoid plan, it proliferates extensively to create a network of chambers and channels, enabling larger body sizes.[5][8]Etymology and Historical Context
The term mesohyl derives from the Greek prefix meso- ("middle") and hylē ("matter" or "wood"), reflecting its role as the intermediary substance within sponge anatomy to specifically denote this gelatinous middle layer.[9] Early observations of sponge internal structures were rudimentary, with microscopists like Robert Grant in the 1820s providing vague accounts of water expulsion from internal cavities, establishing sponges as animals but without precise delineation of the intervening matrix.[10] By the mid-20th century, the layer was commonly termed "mesenchyme" or "mesoglea," with Libbie Hyman clarifying its nature as a supportive gelatinous matrix in her 1940 treatise on invertebrates, emphasizing its role in poriferan organization.[11] The shift to "mesohyl" gained prominence in the 1970s and 1980s, as researchers distinguished the sponge's collagen-rich, largely acellular matrix from the more cellular mesoglea of cnidarians, resolving terminological overlap with vertebrate embryology and highlighting its unique composition.[12] This evolution in nomenclature paralleled advancing histological insights into sponge tissue layers.Structure and Composition
Location and Physical Properties
The mesohyl is located between the outer epithelial layer, known as the pinacoderm, and the inner choanoderm, which lines the water-flow channels within the sponge body.[8] In leuconoid sponges, the most structurally complex form comprising the majority of sponge species, the mesohyl extends throughout the intricate network of incurrent and excurrent canals as well as the flagellated chambers, filling the spaces that support the overall architecture.[13] Physically, the mesohyl exhibits a gelatinous, semi-fluid consistency that provides a flexible scaffold for the sponge.[14] It displays viscoelastic behavior, allowing it to deform under mechanical stress and recover its shape, as observed in species like Chondrosia reniformis where the mesohyl can shift between stiff and pliant states in response to environmental stimuli.[15] Density variations occur across sponge classes; for instance, the mesohyl in calcareous sponges (Calcarea) is typically denser due to the incorporation of abundant calcium carbonate spicules, contrasting with the often lighter, silica-spicule-reinforced mesohyl in demosponges (Demospongiae).[16] This gelatinous matrix functions as an endoskeleton, helping to maintain the sponge's tubular morphology against the forces of water flow during filter feeding.[14] Its thickness ranges from 10–50 μm in thin ectosomal regions of certain homoscleromorph sponges to 550–1,000 μm in subectosomal layers of more robust calcareous sponge species, depending on overall body size and architectural complexity.[17][18]Extracellular Matrix Components
The extracellular matrix of the mesohyl in sponges is primarily composed of collagen proteins, which include fibrillar forms analogous to vertebrate type I collagen and network-forming variants similar to type IV collagen. These collagens provide structural integrity and are secreted by specialized cells such as lophocytes, forming bundled fibrils that contribute to the matrix's tensile strength.[3] In addition to collagens, the matrix contains several adhesion and elasticity-promoting proteins unique to sponge biology, including fibronectin-like molecules that mediate interactions between cells and the extracellular scaffold, galectin which facilitates both cell-cell and cell-matrix binding, and dermatopontin as a minor but essential component enhancing fibril assembly and flexibility. These proteins collectively form a biochemically complex network adapted for the aquatic environment of sponges.[19][20] Embedded within this proteinaceous matrix are skeletal elements that reinforce the mesohyl's architecture. Spicules, rigid needle-like structures, are either siliceous (composed of hydrated silica) in demosponges or calcareous (calcium carbonate-based) in calcareous sponges; they are classified as megascleres for primary load-bearing roles or microscleres for supplementary support and defense. (Hexactinellids, which lack a true mesohyl, possess siliceous spicules in their syncytial tissue.) In certain demosponge groups, particularly keratose species, spongin—a keratin-like, halogenated collagenous protein—forms horny fibers that interweave with spicules or stand alone, providing elasticity and resistance to degradation; as of March 2025, spongin has been found to contain mammalian-like collagens I and III as main structural components.[3][21] The mesohyl matrix overall manifests as a colloidal gel, characterized by intertwined fibrils measuring 10-100 nm in diameter, which create a porous, pH-neutral framework highly hydrated with up to 90% water content to maintain flexibility and facilitate internal transport.[3]Cellular Components
Types of Cells
The mesohyl of sponges harbors a variety of specialized cell types that contribute to the tissue's composition, primarily derived from totipotent stem-like cells. These include amoebocytes, which encompass several subtypes such as archeocytes and collencytes, as well as sclerocytes, spongocytes, and lophocytes.[22][23] Amoebocytes are motile cells characterized by their amoeboid shape and pseudopodia, enabling movement through the mesohyl matrix. Archeocytes, a key subtype, are nucleolated amoeboid cells with non-specific cytoplasmic inclusions, functioning as totipotent stem cells capable of differentiating into other cell types.[23][22] Collencytes produce collagen fibers, often forming nets within their cytoplasm.[24] Sclerocytes are specialized for biomineralization, secreting siliceous or calcareous spicules that form the sponge's skeletal elements. Spongocytes synthesize the protein spongin, an organic fiber that reinforces the mesohyl structure in certain sponge classes. Lophocytes, resembling amoebae, secrete collagen to maintain the mesohyl and move slowly through the tissue.[22][24][25] The mesohyl acts as a dynamic habitat supporting this cellular diversity.[26]Cellular Interactions Within Mesohyl
Cells within the mesohyl of sponges engage in dynamic interactions primarily through adhesion to the extracellular matrix (ECM) and migration along its fibrillar components. Cell-matrix adhesion is mediated by integrins, transmembrane receptors that link the cytoskeleton to ECM proteins such as collagen, facilitating mechanical stability and signaling in this pseudotissue environment.[27] These interactions enable cells like amoebocytes to navigate the mesohyl, migrating along collagen fibrils at speeds up to 15 μm/min, which supports tissue remodeling and reorganization without a fixed epithelial structure.[28] Amoebocytes and other mesohyl cells also participate in collaborative processes, including epithelial-to-mesenchymal transitions that allow cells to shift between stationary and migratory states during regeneration or growth.[29] This mobility contributes to the formation of cell clusters and blastema-like masses, where interactions via filopodia guide collective movement and tissue morphogenesis.[29] Differentiation within the mesohyl is exemplified by archeocytes, totipotent stem-like cells that transform into gametes or somatic cell types during reproduction, driven by signaling pathways embedded in the ECM.[30] Transforming growth factor-β (TGF-β) signaling, enriched in specific mesohyl cell populations, regulates these differentiation events by modulating gene expression for cell fate commitment.[31] The mesohyl thus functions as a responsive pseudotissue, where cells adjust to environmental cues to maintain structural integrity.[32]Functions
Structural and Mechanical Roles
The mesohyl serves as the primary structural framework in sponges, providing mechanical support through its gel-like extracellular matrix reinforced by spicules and, in many species, spongin fibers. The colloidal gel matrix, composed largely of collagen and glycosaminoglycans, offers viscoelastic properties that allow the tissue to withstand compressive forces, while embedded siliceous or calcareous spicules act as rigid skeletal elements to distribute loads and prevent buckling.[3] This composite structure enables resistance to compression, as demonstrated in studies of demosponge tissues where the matrix absorbs energy through molecular rearrangements.[33] In demosponges, spongin—a collagenous protein—further enhances flexibility, permitting the sponge to bend and recover from mechanical stresses imposed by water flow or substrate movement.[7] The mesohyl plays a critical role in maintaining the overall body plan of the sponge by stabilizing the aquiferous system, including incurrent and excurrent canals that form the water-flow network. By filling the spaces between epithelial layers and choanocyte chambers, the mesohyl acts as an endoskeleton that reinforces canal walls against inward collapse during pumping cycles. This support is essential under the low hydrostatic pressures generated by flagellar action, typically ranging from 2 to 50 Pa, ensuring continuous water circulation without deformation of the internal architecture.[34] In leuconoid sponges, which represent the most complex body organization, the mesohyl is particularly vital for reinforcing the numerous flagellated chambers and interconnecting canals, allowing for efficient scaling of body size. This reinforcement distributes mechanical loads across the expanded tissue volume, enabling these sponges to achieve diameters up to 2 m, as seen in large demosponge species like Xestospongia muta. Without the mesohyl's supportive role, such expansive forms would be prone to gravitational sagging or hydrodynamic disruption.[35]Metabolic and Transport Roles
The mesohyl serves as a primary site for nutrient transport in sponges, where its porous structure facilitates the diffusion of dissolved organic matter and other solutes from surrounding seawater into the internal tissues. Amoebocytes, motile cells within the mesohyl, actively shuttle ingested particles and nutrients to various cell types, enabling efficient distribution throughout the sponge body.[36][7][6] Metabolically, the mesohyl supports digestion through archaeocytes, which perform intracellular breakdown of food particles via lysosomal enzymes following phagocytosis. This process allows the sponge to process captured organics into usable forms, contributing to overall energy acquisition. Oxygen diffuses through the mesohyl to sustain aerobic respiration in most regions, though limited diffusion can create anaerobic zones that enable alternative metabolic pathways, such as fermentation by resident microbes.[37][38] A critical aspect of mesohyl metabolism involves symbiotic microorganisms, which can constitute up to 40% of the sponge's total biomass in high-microbial-abundance species and drive carbon and nitrogen cycling by fixing CO₂, oxidizing ammonia, and recycling nutrients. These symbionts enhance the sponge's ability to utilize dissolved organics, with waste products expelled through excurrent pores facilitated by choanocyte-driven water currents.[39][40][41]Evolutionary and Research Context
Evolutionary Significance
The mesohyl represents a primitive extracellular matrix in sponges (Porifera), the earliest-branching metazoan phylum, which diverged from the common ancestor of all animals approximately 600–800 million years ago during the Cryogenian to early Ediacaran periods. A 2025 integrative phylogenomics study has confirmed Porifera as the sister group to all other animals, reinforcing their position at the root of the animal tree.[42] As the structural core between the outer pinacoderm and inner choanoderm, the mesohyl consists of a collagen-rich, gelatinous substance interspersed with motile cells, predating the development of organized true tissues in more derived metazoans. This configuration allowed early sponges to form a cohesive yet flexible body plan without epithelial barriers, facilitating the transition from unicellular choanoflagellate-like ancestors to multicellular filter-feeders.[3][43][44] In comparison to other basal metazoans, the sponge mesohyl is analogous to the mesoglea of cnidarians but exhibits greater cellularity, housing amoeboid cells such as archaeocytes and lophocytes that enable dynamic remodeling and nutrient distribution within the matrix. Cnidarian mesoglea, by contrast, is predominantly acellular and jelly-like, serving primarily as a hydrostatic scaffold between ectoderm and endoderm layers. Furthermore, the absence of a basement membrane in most sponge classes—unlike the collagen IV-lined barriers in eumetazoan epithelia—underscores the non-bilaterian status of Porifera, reflecting an evolutionary stage before the consolidation of polarized tissues and organ systems.[45][46][47] Fossil evidence supports the ancient origins of mesohyl-like structures, with a well-preserved 600-million-year-old Ediacaran sponge-grade fossil, Eocyathispongia qiania, exhibiting a tubular body with internal chambers suggestive of an early mesohyl-supported aquiferous system. These findings indicate that the mesohyl played a pivotal role in enabling the sessile lifestyle of ancestral sponges, providing mechanical stability through collagen and spongin fibers that anchored the body to substrates while accommodating the expansive water-flow network essential for passive feeding. This adaptation likely contributed to the ecological success of sponges as foundational metazoans in Precambrian oceans.[48][3]Current Research and Knowledge Gaps
Recent genomic studies of sponges, initiated in the 2010s, have significantly advanced understanding of mesohyl composition by identifying genes encoding extracellular matrix proteins such as collagens and fibrillins. For instance, the genome of the demosponge Amphimedon queenslandica, sequenced in 2010, revealed upregulated expression of matrix-related genes during the transition to the adult stage, where they contribute to mesohyl formation. Subsequent projects, including single-cell genomics of symbionts in the mesohyl, have highlighted carbohydrate degradation pathways in Poribacteria, a dominant microbial phylum within the matrix. These efforts underscore the mesohyl's role as a genetic hotspot for host-symbiont interactions. Advancements in imaging techniques have enabled detailed visualization of mesohyl cellular architecture. Confocal microscopy, combined with transcriptomics, has mapped 3D distributions of cell types like choanocytes and archeocytes in species such as Ephydatia muelleri, revealing dynamic motile behaviors within the matrix. Live imaging approaches, including optical coherence microscopy, have further elucidated cellular responses in the mesohyl during processes like deflation in Tethya wilhelma. These methods provide high-resolution insights into cell-matrix interactions previously inaccessible through traditional histology. Post-2020 research on microbiome-mesohyl interactions has suggested potential antimicrobial properties mediated by symbionts. Studies using 16S rRNA metagenomics in Red Sea sponges have identified diverse bacterial communities, including Alphaproteobacteria and Roseobacteraceae, that produce bioactive metabolites within the mesohyl for host defense. Metabolomics analyses of Mediterranean sponges have correlated microbial diversification with secondary metabolite production, implying roles in pathogen resistance. However, functional validation of these antimicrobial mechanisms remains pending, as experimental disruptions of symbiont-matrix associations are limited. Despite these progresses, significant knowledge gaps persist in mesohyl biology. Molecular signaling pathways, such as those involving Wnt or NF-κB in cell-matrix communication, are poorly characterized, with current data relying on indirect transcriptomic inferences rather than direct pathway mapping. The mesohyl's role in disease resistance is unclear, particularly regarding how matrix integrity influences susceptibility to emerging fungal pathogens amid global change. Additionally, impacts of climate stressors like ocean warming and acidification on mesohyl structure—such as collagen degradation leading to tissue breakdown—are underexplored, with observational data from heatwave events indicating vulnerability but lacking mechanistic studies.References
- https://en.wiktionary.org/wiki/mesohyl